Keywords
Last Name
Institution

Maria I. New

TitlePROFESSOR
InstitutionMount Sinai
DepartmentEndocrinology - Adrenal Steroid Disorders
Address5 East 98th Street, 10th Floor
New York NY 10029
    Other Positions
    TitlePROFESSOR
    InstitutionMount Sinai
    DepartmentGenetics and Genomic Sciences


     Bibliographic 
     selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Tamma R, Sun L, Cuscito C, Lu P, Corcelli M, Li J, Colaianni G, Moonga SS, Di Benedetto A, Grano M, Colucci S, Yuen T, New MI, Zallone A, Zaidi M. Regulation of bone remodeling by vasopressin explains the bone loss in hyponatremia. Proc Natl Acad Sci U S A. 2013 Nov 12; 110(46):18644-9.
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    2. Sun L, Zhu LL, Lu P, Yuen T, Li J, Ma R, Baliram R, Baliram R, Moonga SS, Liu P, Zallone A, New MI, Davies TF, Zaidi M. Genetic confirmation for a central role for TNFa in the direct action of thyroid stimulating hormone on the skeleton. Proc Natl Acad Sci U S A. 2013 Jun 11; 110(24):9891-6.
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    3. New M, Olzscha H, Liu G, Khan O, Stimson L, McGouran J, Kerr D, Coutts A, Kessler B, Middleton M, La Thangue NB. A regulatory circuit that involves HR23B and HDAC6 governs the biological response to HDAC inhibitors. Cell Death Differ. 2013 Oct; 20(10):1306-16.
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    4. Haider S, Islam B, D'Atri V, Sgobba M, Poojari C, Sun L, Yuen T, Zaidi M, New MI. Structure-phenotype correlations of human CYP21A2 mutations in congenital adrenal hyperplasia. Proc Natl Acad Sci U S A. 2013 Feb 12; 110(7):2605-10.
      View in: PubMed
    5. New MI, Abraham M, Gonzalez B, Dumic M, Razzaghy-Azar M, Chitayat D, Sun L, Zaidi M, Wilson RC, Yuen T. Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Proc Natl Acad Sci U S A. 2013 Feb 12; 110(7):2611-6.
      View in: PubMed
    6. Lekarev O, Tafuri K, Lane AH, Zhu G, Nakamoto JM, Buller-Burckle AM, Wilson TA, New MI. Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene. J Perinatol. 2013 Jan; 33(1):76-8.
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    7. New M, Olzscha H, La Thangue NB. HDAC inhibitor-based therapies: can we interpret the code? Mol Oncol. 2012 Dec; 6(6):637-56.
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    8. New MI, Abraham M, Yuen T, Lekarev O. An update on prenatal diagnosis and treatment of congenital adrenal hyperplasia. Semin Reprod Med. 2012 Oct; 30(5):396-9.
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    9. Zhu LL, Blair H, Cao J, Yuen T, Latif R, Guo L, Tourkova IL, Li J, Davies TF, Sun L, Bian Z, Rosen C, Zallone A, New MI, Zaidi M. Blocking antibody to the ß-subunit of FSH prevents bone loss by inhibiting bone resorption and stimulating bone synthesis. Proc Natl Acad Sci U S A. 2012 Sep 4; 109(36):14574-9.
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    10. Meyer-Bahlburg HF, Dolezal C, Haggerty R, Silverman M, New MI. Cognitive outcome of offspring from dexamethasone-treated pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Eur J Endocrinol. 2012 Jul; 167(1):103-10.
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    11. Rabbani B, Mahdieh N, Sayarifar F, Ashtiani MT, New M, Parsa A, Akbari MT, Rabbani A. A girl with 45,X/46,XX Turner syndrome and salt wasting form of congenital adrenal hyperplasia due to regulatory changes. Clin Lab. 2012; 58(9-10):1063-6.
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    12. Lekarev O, New MI. Adrenal disease in pregnancy. Best Pract Res Clin Endocrinol Metab. 2011 Dec; 25(6):959-73.
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    13. Lekarev O, Mallet D, Yuen T, Morel Y, New MI. Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein gene. Eur J Pediatr. 2012 May; 171(5):787-93.
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    14. Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Barta C, Lu RB, Zhukova OV, Kim JJ, Siniscalco M, New M, Li H, Kajuna SL, Manolopoulos VG, Speed WC, Pakstis AJ, Kidd JR, Kidd KK. A global view of the OCA2-HERC2 region and pigmentation. Hum Genet. 2012 May; 131(5):683-96.
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    15. Rabbani B, Mahdieh N, Ashtiani MT, Larijani B, Akbari MT, New M, Parsa A, Schouten JP, Rabbani A. Mutation analysis of the CYP21A2 gene in the Iranian population. Genet Test Mol Biomarkers. 2012 Feb; 16(2):82-90.
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    16. Nimkarn S, Lin-Su K, New MI. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia. Pediatr Clin North Am. 2011 Oct; 58(5):1281-300, xii.
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    17. Willis KJ, Feurdean A, Birks HJ, Bjune AE, Breman E, Broekman R, Grytnes JA, New M, Singarayer JS, Rozema J. Quantification of UV-B flux through time using UV-B-absorbing compounds contained in fossil Pinus sporopollenin. New Phytol. 2011 Oct; 192(2):553-60.
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    18. McEvoy MP, Rich BS, New M, Tang LH, La Quaglia MP. Thymic carcinoid presenting with Cushing's syndrome in a 17-year-old boy: a case report and review of the literature. J Clin Oncol. 2011 Sep 1; 29(25):e716-8.
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    19. Parsa AA, New MI. Low-renin hypertension of childhood. Endocrinol Metab Clin North Am. 2011 Jun; 40(2):369-77, viii.
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    20. Lin-Su K, Harbison MD, Lekarev O, Vogiatzi MG, New MI. Final adult height in children with congenital adrenal hyperplasia treated with growth hormone. J Clin Endocrinol Metab. 2011 Jun; 96(6):1710-7.
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    21. George MM, Sinha S, Mamkin I, Philibert P, New MI, Wilson RC, Sultan C, Ten S, Bhangoo A. Isolated mild clitoral hypertrophy may reveal 46,XY disorders of sex development in infancy due to 17ßHSD-3 defect confirmed by molecular analysis. Gynecol Endocrinol. 2011 Nov; 27(11):890-4.
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    22. Dumic M, New MI, Lin-Su K, McElreavey K, Leibel NI, Ciglar S, Nimkarn S, Vinci G, Wilson J, Lasan R. Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual development. Adv Exp Med Biol. 2011; 707:169-70.
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    23. New MI, Parsa AA. Long range outcome of prenatal treatment. Adv Exp Med Biol. 2011; 707:33-5.
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    24. Harbison MD, Lin-Su K, New MI. Growth hormone treatment in children with congenital adrenal hyperplasia. Adv Exp Med Biol. 2011; 707:107.
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    25. Lekarev O, Morel Y, New MI. Atypical presentation and novel star protein gene mutation in a 46,XY female with lipoid congenital adrenal hyperplasia. Adv Exp Med Biol. 2011; 707:133-4.
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    26. New MI. Ancient history of congenital adrenal hyperplasia. Endocr Dev. 2011; 20:202-11.
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    27. New MI. Vindication of prenatal diagnosis and treatment of congenital adrenal hyperplasia with low-dose dexamethasone. Am J Bioeth. 2010 Dec; 10(12):67-8.
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    28. New M. Description and defense of prenatal diagnosis and treatment with low-dose dexamethasone for congenital adrenal hyperplasia. Am J Bioeth. 2010 Sep; 10(9):48-51.
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    29. George MM, New MI, Ten S, Sultan C, Bhangoo A. The clinical and molecular heterogeneity of 17ßHSD-3 enzyme deficiency. Horm Res Paediatr. 2010; 74(4):229-40.
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    30. Nimkarn S, New MI. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A paradigm for prenatal diagnosis and treatment. Ann N Y Acad Sci. 2010 Mar; 1192:5-11.
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    31. Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Mehdi SQ, Kajuna SL, Barta C, Kungulilo S, Karoma NJ, Lu RB, Zhukova OV, Kim JJ, Comas D, Siniscalco M, New M, Li P, Li H, Manolopoulos VG, Speed WC, Rajeevan H, Pakstis AJ, Kidd JR, Kidd KK. The distribution and most recent common ancestor of the 17q21 inversion in humans. Am J Hum Genet. 2010 Feb 12; 86(2):161-71.
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    32. Dumic K, Wilson R, Thanasawat P, Grubic Z, Kusec V, Stingl K, New MI. Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other. Eur J Pediatr. 2010 Jul; 169(7):891-4.
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    33. Nimkarn S, Lin-Su K, New MI. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia. Endocrinol Metab Clin North Am. 2009 Dec; 38(4):699-718.
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    34. Guevarra FM, Nimkarn S, New MI, Lin-Su K. Long-term growth hormone therapy in an adolescent boy with 45,X/46,XidicY(p11). J Pediatr. 2009 Nov; 155(5):752-5.e1-3.
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    35. Bas F, Kayserili H, Darendeliler F, Uyguner O, Günöz H, Yüksel Apak M, Atalar F, Bundak R, Wilson RC, New MI, Wollnik B, Saka N. CYP21A2 gene mutations in congenital adrenal hyperplasia: genotype-phenotype correlation in Turkish children. J Clin Res Pediatr Endocrinol. 2009; 1(3):116-28.
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    36. Quintos JB, Krotz S, Vogiatzi MG, Kralickova M, New MI. Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor. J Pediatr Endocrinol Metab. 2009 Feb; 22(2):181-5.
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    37. Nimkarn S, New MI. Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Mol Cell Endocrinol. 2009 Mar 5; 300(1-2):192-6.
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    38. Guevarra FM, New MI. Mutation of growth hormone receptor in children with Idiopathic Short Stature. Mt Sinai J Med. 2008 Dec 1; 75(6):556-7.
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    39. Jacovina A, New M. Chemokine (C-C motif) receptor 5 entry inhibitors: new class of drugs for acquired immune deficiency syndrome. Mt Sinai J Med. 2008 May-Jun; 75(3):297-8.
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    40. Ten S, Bhangoo A, Ramchandani N, Mueller C, Vogiatzi M, New M, Lesser M, Maclaren N. Resting energy expenditure in insulin resistance falls with decompensation of insulin secretion in obese children. J Pediatr Endocrinol Metab. 2008 Apr; 21(4):359-67.
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    41. Funder J, New MI. Low renin hypertension (LRH): shades of John Laragh. Trends Endocrinol Metab. 2008 Apr; 19(3):83.
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    42. Dumic M, Lin-Su K, Leibel NI, Ciglar S, Vinci G, Lasan R, Nimkarn S, Wilson JD, McElreavey K, New MI. Report of fertility in woman with predominantly 46,XY karyotype in family with multiple disorders of sexual development: review of prismatic case. Mt Sinai J Med. 2008 Mar-Apr; 75(2):168-9.
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    43. Nimkarn S, New MI. Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia. Trends Endocrinol Metab. 2008 Apr; 19(3):96-9.
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    44. Meyer-Bahlburg HF, Dolezal C, Baker SW, New MI. Sexual orientation in women with classical or non-classical congenital adrenal hyperplasia as a function of degree of prenatal androgen excess. Arch Sex Behav. 2008 Feb; 37(1):85-99.
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    45. Lin-Su K, New MI. Inactivation of the acid labile subunit gene resulting in insulin-like growth factor deficiency. Mt Sinai J Med. 2008 Jan-Feb; 75(1):57-8.
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    46. Lin-Su K, Nimkarn S, New MI. Congenital adrenal hyperplasia in adolescents: diagnosis and management. Ann N Y Acad Sci. 2008; 1135:95-8.
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    47. Dumic M, Lin-Su K, Leibel NI, Ciglar S, Vinci G, Lasan R, Nimkarn S, Wilson JD, McElreavey K, New MI. Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual development. J Clin Endocrinol Metab. 2008 Jan; 93(1):182-9.
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    48. Lin-Su K, New MI. Effects of adrenal steroids on the bone metabolism of children with congenital adrenal hyperplasia. Ann N Y Acad Sci. 2007 Nov; 1117:345-51.
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    49. Ten S, Bhangoo A, Ramchandani N, Mueller C, Vogiatzi M, New M, Lesser M, Maclaren N. Characterization of insulin resistance syndrome in children and young adults. When to screen for prediabetes? J Pediatr Endocrinol Metab. 2007 Sep; 20(9):989-99.
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    50. Trinh L, Nimkarn S, New MI, Lin-Su K. Growth and pubertal characteristics in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Pediatr Endocrinol Metab. 2007 Aug; 20(8):883-91.
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    51. Messer CK, Kirschenbaum A, New MI, Unger P, Gabrilove JL, Levine AC. Concomitant secretion of glucocorticoid, androgens, and mineralocorticoid by an adrenocortical carcinoma: case report and review of literature. Endocr Pract. 2007 Jul-Aug; 13(4):408-12.
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    52. Nimkarn S, New MI. Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Nat Clin Pract Endocrinol Metab. 2007 May; 3(5):405-13.
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    53. New MI. Apparent mineralocorticoid excess manifested in an elderly patient with hypothyroidism. Mt Sinai J Med. 2007 Apr; 74(1):40-1.
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    54. Wilson RC, Nimkarn S, Dumic M, Obeid J, Azar MR, Azar M, Najmabadi H, Saffari F, New MI. Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Mol Genet Metab. 2007 Apr; 90(4):414-21.
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    55. Nimkarn S, New MI. Prenatal diagnosis and treatment of congenital adrenal hyperplasia. Pediatr Endocrinol Rev. 2006 Dec-2007 Jan; 4(2):99-105.
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    56. Meyer-Bahlburg HF, Dolezal C, Zucker KJ, Kessler SJ, Schober JM, New MI. The Recalled Childhood Gender Questionnaire-Revised: a psychometric analysis in a sample of women with congenital adrenal hyperplasia. J Sex Res. 2006 Nov; 43(4):364-7.
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    57. Nimkarn S, New MI. Prenatal diagnosis and treatment of congenital adrenal hyperplasia. Horm Res. 2007; 67(2):53-60.
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    58. Nimkarn S, Lin-Su K, Berglind N, Wilson RC, New MI. Aldosterone-to-renin ratio as a marker for disease severity in 21-hydroxylase deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2007 Jan; 92(1):137-42.
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    59. New MI. Congenital adrenal hyperplasia and poverty. J Pediatr Endocrinol Metab. 2006 Oct; 19(10):1191.
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    60. Chalmers LJ, Casas L, New MI, Blackett PR. Prolongation of growth by treatment of 11-hydroxylase deficiency with depot-leuprolide, growth hormone, and hydrocortisone. J Pediatr Endocrinol Metab. 2006 Oct; 19(10):1251-5.
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    61. Bhangoo A, Wilson R, New MI, Ten S. Donor splice mutation in the 11beta-hydroxylase (CypllB1) gene resulting in sex reversal: a case report and review of the literature. J Pediatr Endocrinol Metab. 2006 Oct; 19(10):1267-82.
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    62. New MI. Extensive clinical experience: nonclassical 21-hydroxylase deficiency. J Clin Endocrinol Metab. 2006 Nov; 91(11):4205-14.
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    63. Meyer-Bahlburg HF, Dolezal C, Baker SW, Ehrhardt AA, New MI. Gender development in women with congenital adrenal hyperplasia as a function of disorder severity. Arch Sex Behav. 2006 Dec; 35(6):667-84.
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    64. Ergun-Longmire B, Auchus R, Papari-Zareei M, Tansil S, Wilson RC, New MI. Two novel mutations found in a patient with 17alpha-hydroxylase enzyme deficiency. J Clin Endocrinol Metab. 2006 Oct; 91(10):4179-82.
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    65. New MI. Nonclassic 21-hydroxylase deficiency. Fertil Steril. 2006 Jul; 86 Suppl 1:S2.
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    66. Dumic M, Janjanin N, Ille J, Zunec R, Spehar A, Zlopasa G, Francetic I, New MI. Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Pediatr Endocrinol Metab. 2005 Sep; 18(9):887-95.
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    67. Ergun-Longmire B, Vinci G, Alonso L, Matthew S, Tansil S, Lin-Su K, McElreavey K, New MI. Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature. J Pediatr Endocrinol Metab. 2005 Aug; 18(8):739-48.
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    68. So A, Duffy DL, Gordon RD, Jeske YW, Lin-Su K, New MI, Stowasser M. Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity. J Hypertens. 2005 Aug; 23(8):1477-84.
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    69. Keen-Kim D, Redman JB, Alanes RU, Eachus MM, Wilson RC, New MI, Nakamoto JM, Fenwick RG. Validation and clinical application of a locus-specific polymerase chain reaction- and minisequencing-based assay for congenital adrenal hyperplasia (21-hydroxylase deficiency). J Mol Diagn. 2005 May; 7(2):236-46.
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    70. New MI, Geller DS, Fallo F, Wilson RC. Monogenic low renin hypertension. Trends Endocrinol Metab. 2005 Apr; 16(3):92-7.
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    71. Lin-Su K, Vogiatzi MG, Marshall I, Harbison MD, Macapagal MC, Betensky B, Tansil S, New MI. Treatment with growth hormone and luteinizing hormone releasing hormone analog improves final adult height in children with congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2005 Jun; 90(6):3318-25.
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    72. Motaghedi R, Betensky BP, Slowinska B, Cerame B, Cabrer M, New MI, Wilson RC. Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency. J Pediatr Endocrinol Metab. 2005 Feb; 18(2):133-42.
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    73. Chemaitilly W, Betensky BP, Marshall I, Wei JQ, Wilson RC, New MI. The natural history and genotype-phenotype nonconcordance of HLA identical siblings with the same mutations of the 21-hydroxylase gene. J Pediatr Endocrinol Metab. 2005 Feb; 18(2):143-53.
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    74. New MI. An update of congenital adrenal hyperplasia. Ann N Y Acad Sci. 2004 Dec; 1038:14-43.
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    75. Lin-Su K, Zhou P, Arora N, Betensky BP, New MI, Wilson RC. In vitro expression studies of a novel mutation delta299 in a patient affected with apparent mineralocorticoid excess. J Clin Endocrinol Metab. 2004 May; 89(5):2024-7.
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    76. Meyer-Bahlburg HF, Dolezal C, Baker SW, Carlson AD, Obeid JS, New MI. Prenatal androgenization affects gender-related behavior but not gender identity in 5-12-year-old girls with congenital adrenal hyperplasia. Arch Sex Behav. 2004 Apr; 33(2):97-104.
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    77. Dumic M, Ille J, Zunec R, Plavsic V, Francetic I, Skrabic V, Janjanin N, Spehar A, Wei J, Wilson RC, New MI. Nonclassic 21-hydroxylase deficiency in Croatia. J Pediatr Endocrinol Metab. 2004 Feb; 17(2):157-64.
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    78. Meyer-Bahlburg HF, Dolezal C, Baker SW, Carlson AD, Obeid JS, New MI. Cognitive and motor development of children with and without congenital adrenal hyperplasia after early-prenatal dexamethasone. J Clin Endocrinol Metab. 2004 Feb; 89(2):610-4.
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    79. New MI. Inborn errors of adrenal steroidogenesis. Mol Cell Endocrinol. 2003 Dec 15; 211(1-2):75-83.
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    80. Tukel T, Uyguner O, Wei JQ, Yuksel-Apak M, Saka N, Song DX, Kayserili H, Bas F, Gunoz H, Wilson RC, New MI, Wollnik B. A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency. J Clin Endocrinol Metab. 2003 Dec; 88(12):5893-7.
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    81. Chemaitilly W, Wilson RC, New MI. Hypertension and adrenal disorders. Curr Hypertens Rep. 2003 Dec; 5(6):498-504.
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    82. Marshall I, Ugrasbul F, Manginello F, Wajnrajch MP, Shackleton CH, New MI, Vogiatzi MV. Congenital hypopituitarism as a cause of undetectable estriol levels in the maternal triple-marker screen. J Clin Endocrinol Metab. 2003 Sep; 88(9):4144-8.
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    83. New M. Hypertension in congenital adrenal hyperplasia and apparent mineralocorticoid excess. Ann N Y Acad Sci. 2002 Sep; 970:145-54.
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    84. Lin-Su K, Vogiatzi MG, New MI. Body mass index and age at menarche in an adolescent clinic population. Clin Pediatr (Phila). 2002 Sep; 41(7):501-7.
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    85. Charmandari E, Eisenhofer G, Mehlinger SL, Carlson A, Wesley R, Keil MF, Chrousos GP, New MI, Merke DP. Adrenomedullary function may predict phenotype and genotype in classic 21-hydroxylase deficiency. J Clin Endocrinol Metab. 2002 Jul; 87(7):3031-7.
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    86. Gmyrek GA, New MI, Sosa RE, Poppas DP. Bilateral laparoscopic adrenalectomy as a treatment for classic congenital adrenal hyperplasia attributable to 21-hydroxylase deficiency. Pediatrics. 2002 Feb; 109(2):E28.
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    87. New MI, Carlson A, Obeid J, Marshall I, Cabrera MS, Goseco A, Lin-Su K, Putnam AS, Wei JQ, Wilson RC. Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies. J Clin Endocrinol Metab. 2001 Dec; 86(12):5651-7.
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    88. Cabrera MS, Vogiatzi MG, New MI. Long term outcome in adult males with classic congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2001 Jul; 86(7):3070-8.
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    89. New MI. Factors determining final height in congenital adrenal hyperplasia. J Pediatr Endocrinol Metab. 2001 Jul; 14 Suppl 2:933-7.
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    90. Ten S, New M, Maclaren N. Clinical review 130: Addison's disease 2001. J Clin Endocrinol Metab. 2001 Jul; 86(7):2909-22.
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    91. Quintos JB, Vogiatzi MG, Harbison MD, New MI. Growth hormone therapy alone or in combination with gonadotropin-releasing hormone analog therapy to improve the height deficit in children with congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2001 Apr; 86(4):1511-7.
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    92. Wilson RC, Nimkarn S, New MI. Apparent mineralocorticoid excess. Trends Endocrinol Metab. 2001 Apr; 12(3):104-11.
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    93. Wajnrajch MP, Gertner JM, Huma Z, Popovic J, Lin K, Verlander PC, Batish SD, Giampietro PF, Davis JG, New MI, Auerbach AD. Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry. Pediatrics. 2001 Apr; 107(4):744-54.
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    94. New MI. Prenatal treatment of congenital adrenal hyperplasia: author differs with technical report. Pediatrics. 2001 Apr; 107(4):804.
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    95. New MI. Prenatal treatment of congenital adrenal hyperplasia. The United States experience. Endocrinol Metab Clin North Am. 2001 Mar; 30(1):1-13.
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    96. Fisch H, Golden RJ, Libersen GL, Hyun GS, Madsen P, New MI, Hensle TW. Maternal age as a risk factor for hypospadias. J Urol. 2001 Mar; 165(3):934-6.
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    97. Newfield RS, Spitz IM, Isacson C, New MI. Long-term mifepristone (RU486) therapy resulting in massive benign endometrial hyperplasia. Clin Endocrinol (Oxf). 2001 Mar; 54(3):399-404.
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    98. New M. Arthritis: an impending public health epidemic. J Okla State Med Assoc. 2001 Feb; 94(2):63-4.
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    99. New MI. Antenatal diagnosis and treatment of congenital adrenal hyperplasia. Curr Urol Rep. 2001 Feb; 2(1):11-8.
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    100. New MI, Nimkarn S, Brandon DD, Cunningham-Rundles S, Wilson RC, Newfield RS, Vandermeulen J, Barron N, Russo C, Loriaux DL, O'Malley B. Resistance to multiple steroids in two sisters. J Steroid Biochem Mol Biol. 2001 Jan-Mar; 76(1-5):161-6.
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    101. Cerame BI, New MI. Hormonal hypertension in children: 11beta-hydroxylase deficiency and apparent mineralocorticoid excess. J Pediatr Endocrinol Metab. 2000 Nov-Dec; 13(9):1537-47.
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    102. New M, Berliner L. Mental health service utilization by victims of crime. J Trauma Stress. 2000 Oct; 13(4):693-707.
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    103. New MI. Citation for the 2000 Gerald D. Aurbach Award Lecture of The Endocrine Society to Dr. Marvin Gershengorn. Endocr Rev. 2000 Aug; 21(4):450-1.
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    104. Newfield RS, Kalaitzoglou G, Licholai T, Chilton D, Ashraf J, Thompson EB, New MI. Normocortisolemic Cushing's syndrome initially presenting with increased glucocorticoid receptor numbers. J Clin Endocrinol Metab. 2000 Jan; 85(1):14-21.
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    105. New MI, Obeid J, Wilson RC, Cabrera MS, Goseco A, Macapagal MC, Marshall I, Nimkarn S, Quintos JB, Ten S, Ugrasbul F, Vandermolen L, Harbison MD. Profile of the pediatric endocrine clinic at New York-Presbyterian Hospital, New York Weill Cornell Center. J Clin Endocrinol Metab. 1999 Dec; 84(12):4444-9.
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    106. New MI, Nimkarn S, Brandon DD, Cunningham-Rundles S, Wilson RC, Newfield RS, Vandermeulen J, Barron N, Russo C, Loriaux DL, O'Malley B. Resistance to several steroids in two sisters. J Clin Endocrinol Metab. 1999 Dec; 84(12):4454-64.
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    107. Ugrasbul F, Wiens T, Rubinstein P, New MI, Wilson RC. Prevalence of mild apparent mineralocorticoid excess in Mennonites. J Clin Endocrinol Metab. 1999 Dec; 84(12):4735-8.
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    108. Spiro RP, Christian SL, Ledbetter DH, New MI, Wilson RC, Roizen N, Rosenfield RL. Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasia. Pediatr Res. 1999 Nov; 46(5):510-3.
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    109. New MI, Wilson RC. Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess. Proc Natl Acad Sci U S A. 1999 Oct 26; 96(22):12790-7.
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    110. Cerame BI, Newfield RS, Pascoe L, Curnow KM, Nimkarn S, Roe TF, New MI, Wilson RC. Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia. J Clin Endocrinol Metab. 1999 Sep; 84(9):3129-34.
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    111. Carlson AD, Obeid JS, Kanellopoulou N, Wilson RC, New MI. Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment. J Steroid Biochem Mol Biol. 1999 Apr-Jun; 69(1-6):19-29.
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    112. Damore ME, Speiser PW, Slonim AE, New MI, Shanske S, Xia W, Santorelli FM, DiMauro S. Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review. J Pediatr Endocrinol Metab. 1999 Mar-Apr; 12(2):207-13.
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    113. Nimkarn S, Cerame BI, Wei JQ, Dumic M, Zunec R, Brkljacic L, Skrabic V, New MI, Wilson RC. Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutations. J Clin Endocrinol Metab. 1999 Jan; 84(1):378-81.
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    114. Berliner L, New M. The impact of health care reform: a survey of victim and offender treatment providers. Sex Abuse. 1999 Jan; 11(1):5-16.
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    115. Wilson RC, Dave-Sharma S, Wei JQ, Obeyesekere VR, Li K, Ferrari P, Krozowski ZS, Shackleton CH, Bradlow L, Wiens T, New MI. A genetic defect resulting in mild low-renin hypertension. Proc Natl Acad Sci U S A. 1998 Aug 18; 95(17):10200-5.
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    116. Skuse D, Bentovim A, Hodges J, Stevenson J, Andreou C, Lanyado M, New M, Williams B, McMillan D. Risk factors for development of sexually abusive behaviour in sexually victimised adolescent boys: cross sectional study. BMJ. 1998 Jul 18; 317(7152):175-9.
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    117. Dave-Sharma S, Wilson RC, Harbison MD, Newfield R, Azar MR, Krozowski ZS, Funder JW, Shackleton CH, Bradlow HL, Wei JQ, Hertecant J, Moran A, Neiberger RE, Balfe JW, Fattah A, Daneman D, Akkurt HI, De Santis C, New MI. Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess. J Clin Endocrinol Metab. 1998 Jul; 83(7):2244-54.
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    118. Calleja EM, Shen JY, Lesser M, Grady RW, New MI, Giardina PJ. Survival and morbidity in transfusion-dependent thalassemic patients on subcutaneous desferrioxamine chelation. Nearly two decades of experience. Ann N Y Acad Sci. 1998 Jun 30; 850:469-70.
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    119. New MI. Inborn errors of steroidogenesis. Steroids. 1998 May-Jun; 63(5-6):238-42.
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    120. Zhang YH, Guo W, Wagner RL, Huang BL, McCabe L, Vilain E, Burris TP, Anyane-Yeboa K, Burghes AH, Chitayat D, Chudley AE, Genel M, Gertner JM, Klingensmith GJ, Levine SN, Nakamoto J, New MI, Pagon RA, Pappas JG, Quigley CA, Rosenthal IM, Baxter JD, Fletterick RJ, McCabe ER. DAX1 mutations map to putative structural domains in a deduced three-dimensional model. Am J Hum Genet. 1998 Apr; 62(4):855-64.
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    121. New M, Melvin D, Trickett S. Community support to families living with HIV in London: an agency overview. AIDS Care. 1998 Apr; 10(2):191-6.
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    122. Quercia N, Chitayat D, Babul-Hirji R, New MI, Daneman D. Normal external genitalia in a female with classical congenital adrenal hyperplasia who was not treated during embryogenesis. Prenat Diagn. 1998 Jan; 18(1):83-5.
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    123. New MI. Diagnosis and management of congenital adrenal hyperplasia. Annu Rev Med. 1998; 49:311-28.
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    124. Litchfield WR, New MI, Coolidge C, Lifton RP, Dluhy RG. Evaluation of the dexamethasone suppression test for the diagnosis of glucocorticoid-remediable aldosteronism. J Clin Endocrinol Metab. 1997 Nov; 82(11):3570-3.
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    125. Dumic M, Brkljacic L, Plavsic V, Zunec R, Ille J, Wilson RC, Kuvacic I, Kastelan A, New MI. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) in Croatia. Am J Med Genet. 1997 Oct 31; 72(3):302-6.
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    126. Newfield RS, New MI. 21-hydroxylase deficiency. Ann N Y Acad Sci. 1997 Jun 17; 816:219-29.
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    127. New M. Sterne and The history of cold-bathing. Notes Queries. 1997 Jun; 44(2):211-2.
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    128. New MI. Changes in The Journal of Clinical Endocrinology and Metabolism--an editorial from Dr. Maria I. New, Editor-in-Chief. J Clin Endocrinol Metab. 1997 Jun; 82(6):1655.
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    129. Nass R, Heier L, Moshang T, Oberfield S, George A, New MI, Speiser PW. Magnetic resonance imaging in the congenital adrenal hyperplasia population: increased frequency of white-matter abnormalities and temporal lobe atrophy. J Child Neurol. 1997 Apr; 12(3):181-6.
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    130. New MI, Newfield RS. Congenital adrenal hyperplasia. Curr Ther Endocrinol Metab. 1997; 6:179-87.
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    131. Meyer-Bahlburg HF, Gruen RS, New MI, Bell JJ, Morishima A, Shimshi M, Bueno Y, Vargas I, Baker SW. Gender change from female to male in classical congenital adrenal hyperplasia. Horm Behav. 1996 Dec; 30(4):319-32.
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    132. Trautman PD, Meyer-Bahlburg HF, Postelnek J, New MI. Mothers' reactions to prenatal diagnostic procedures and dexamethasone treatment of congenital adrenal hyperplasia. J Psychosom Obstet Gynaecol. 1996 Sep; 17(3):175-81.
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    133. New MI. Treatment-induced hypoandrogenism in childhood and puberty in females with virilizing (21-hydroxylase deficiency) congenital adrenal hyperplasia. J Endocrinol. 1996 Sep; 150 Suppl:S31-2.
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    134. Van Wyk JJ, Gunther DF, Ritzén EM, Wedell A, Cutler GB, Migeon CJ, New MI. The use of adrenalectomy as a treatment for congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1996 Sep; 81(9):3180-90.
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    135. Vogiatzi MG, Boeck MA, Vlachopapadopoulou E, el-Rashid R, New MI. Dehydroepiandrosterone in morbidly obese adolescents: effects on weight, body composition, lipids, and insulin resistance. Metabolism. 1996 Aug; 45(8):1011-5.
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    136. Ferrari P, Obeyesekere VR, Li K, Wilson RC, New MI, Funder JW, Krozowski ZS. Point mutations abolish 11 beta-hydroxysteroid dehydrogenase type II activity in three families with the congenital syndrome of apparent mineralocorticoid excess. Mol Cell Endocrinol. 1996 May 17; 119(1):21-4.
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    137. Andersson S, Geissler WM, Wu L, Davis DL, Grumbach MM, New MI, Schwarz HP, Blethen SL, Mendonca BB, Bloise W, Witchel SF, Cutler GB, Griffin JE, Wilson JD, Russel DW. Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiency. J Clin Endocrinol Metab. 1996 Jan; 81(1):130-6.
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    138. Obeyesekere VR, Ferrari P, Andrews RK, Wilson RC, New MI, Funder JW, Krozowski ZS. The R337C mutation generates a high Km 11 beta-hydroxysteroid dehydrogenase type II enzyme in a family with apparent mineralocorticoid excess. J Clin Endocrinol Metab. 1995 Nov; 80(11):3381-3.
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    139. Wilson RC, Mercado AB, Cheng KC, New MI. Steroid 21-hydroxylase deficiency: genotype may not predict phenotype. J Clin Endocrinol Metab. 1995 Aug; 80(8):2322-9.
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    140. New MI, White PC. Genetic disorders of steroid hormone synthesis and metabolism. Baillieres Clin Endocrinol Metab. 1995 Jul; 9(3):525-54.
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    141. Wilson RC, Krozowski ZS, Li K, Obeyesekere VR, Razzaghy-Azar M, Harbison MD, Wei JQ, Shackleton CH, Funder JW, New MI. A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess. J Clin Endocrinol Metab. 1995 Jul; 80(7):2263-6.
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    142. Mercado AB, Wilson RC, Cheng KC, Wei JQ, New MI. Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency. J Clin Endocrinol Metab. 1995 Jul; 80(7):2014-20.
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    143. Simard J, Rheaume E, Mebarki F, Sanchez R, New MI, Morel Y, Labrie F. Molecular basis of human 3 beta-hydroxysteroid dehydrogenase deficiency. J Steroid Biochem Mol Biol. 1995 Jun; 53(1-6):127-38.
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    144. Wilson RC, Wei JQ, Cheng KC, Mercado AB, New MI. Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene. J Clin Endocrinol Metab. 1995 May; 80(5):1635-40.
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    145. New MI. Steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia). Am J Med. 1995 Jan 16; 98(1A):2S-8S.
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    146. Trautman PD, Meyer-Bahlburg HF, Postelnek J, New MI. Effects of early prenatal dexamethasone on the cognitive and behavioral development of young children: results of a pilot study. Psychoneuroendocrinology. 1995; 20(4):439-49.
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    147. Speiser PW, Heier L, Serrat J, New MI, Nass R. Failure of steroid replacement to consistently normalize pituitary function in congenital adrenal hyperplasia: hormonal and MRI data. Horm Res. 1995; 44(6):241-6.
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    148. Zerah M, Rhéaume E, Mani P, Schram P, Simard J, Labrie F, New MI. No evidence of mutations in the genes for type I and type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) in nonclassical 3 beta HSD deficiency. J Clin Endocrinol Metab. 1994 Dec; 79(6):1811-7.
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    149. Speiser PW, New MI. Prenatal diagnosis and management of congenital adrenal hyperplasia. Clin Perinatol. 1994 Sep; 21(3):631-45.
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    150. New MI. The prismatic case of apparent mineralocorticoid excess. J Clin Endocrinol Metab. 1994 Jul; 79(1):1-3.
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    151. Rittmaster RS, Antonian L, New MI, Stoner E. Effect of finasteride on adrenal steroidogenesis in men. J Androl. 1994 Jul-Aug; 15(4):298-301.
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    152. Speiser PW, New MI. Prenatal diagnosis and treatment of congenital adrenal hyperplasia. J Pediatr Endocrinol. 1994 Jul-Sep; 7(3):183-91.
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    153. Speiser PW, White PC, Dupont J, Zhu D, Mercado AB, New MI. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot. Hum Genet. 1994 Apr; 93(4):424-8.
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    154. Wigley WC, Prihoda JS, Mowszowicz I, Mendonca BB, New MI, Wilson JD, Russell DW. Natural mutagenesis study of the human steroid 5 alpha-reductase 2 isozyme. Biochemistry. 1994 Feb 8; 33(5):1265-70.
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    155. New MI. Apparent mineralocorticoid excess: a personal history. Steroids. 1994 Feb; 59(2):66-8.
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    156. New MI. 21-hydroxylase deficiency congenital adrenal hyperplasia. J Steroid Biochem Mol Biol. 1994 Jan; 48(1):15-22.
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    157. Speiser PW, White PC, Dupont J, Zhu D, Mercado A, New MI. Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization. Recent Prog Horm Res. 1994; 49:367-71.
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    158. White PC, Tusie-Luna MT, New MI, Speiser PW. Mutations in steroid 21-hydroxylase (CYP21). Hum Mutat. 1994; 3(4):373-8.
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    159. Ueshiba H, Zerah M, New MI. Enzyme-linked immunosorbent assay (ELISA) method for screening of non-classical steroid 21-hydroxylase deficiency. Horm Metab Res. 1994 Jan; 26(1):43-5.
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    160. Qin KN, New MI, Cheng KC. Molecular cloning of multiple cDNAs encoding human enzymes structurally related to 3 alpha-hydroxysteroid dehydrogenase. J Steroid Biochem Mol Biol. 1993 Dec; 46(6):673-9.
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    161. Nikkilä H, Tannin GM, New MI, Taylor NF, Kalaitzoglou G, Monder C, White PC. Defects in the HSD11 gene encoding 11 beta-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency. J Clin Endocrinol Metab. 1993 Sep; 77(3):687-91.
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    162. Speiser PW, Riddick LM, Martin K, New MI. Investigation of the mechanism of hypertension in apparent mineralocorticoid excess. Metabolism. 1993 Jul; 42(7):843-5.
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    163. New MI. Nonclassical congenital adrenal hyperplasia and the polycystic ovarian syndrome. Ann N Y Acad Sci. 1993 May 28; 687:193-205.
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    164. Curnow KM, Slutsker L, Vitek J, Cole T, Speiser PW, New MI, White PC, Pascoe L. Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8. Proc Natl Acad Sci U S A. 1993 May 15; 90(10):4552-6.
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    165. New MI, Kitzinger ES. Pope Joan: a recognizable syndrome. J Clin Endocrinol Metab. 1993 Jan; 76(1):3-13.
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    166. New MI. Pope Joan: a recognizable syndrome. Trans Am Clin Climatol Assoc. 1993; 104:104-22.
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    167. Kalaitzoglou G, New MI. Congenital adrenal hyperplasia. Molecular insights learned from patients. Receptor. 1993; 3(3):211-22.
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    168. Speiser PW, Serrat J, New MI, Gertner JM. Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency. J Clin Endocrinol Metab. 1992 Dec; 75(6):1421-4.
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    169. Carré-Eusèbe D, Imbeaud S, Harbison M, New MI, Josso N, Picard JY. Variants of the anti-Müllerian hormone gene in a compound heterozygote with the persistent Müllerian duct syndrome and his family. Hum Genet. 1992 Dec; 90(4):389-94.
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    170. New MI. Female pseudohermaphroditism. Semin Perinatol. 1992 Oct; 16(5):299-318.
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    171. Johnson V, New MI. If the stimulus to pituitary thyroid-stimulating hormone (TSH) secretion is the lack of circulating free thyroxine (free-T4) why may a baby with congenital nephrotic syndrome present with a raised TSH on neonatal screening? Pediatr Nephrol. 1992 Sep; 6(5):458.
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    172. Pascoe L, Curnow KM, Slutsker L, Connell JM, Speiser PW, New MI, White PC. Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2. Proc Natl Acad Sci U S A. 1992 Sep 1; 89(17):8327-31.
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    173. Speiser PW, Dupont J, Zhu D, Serrat J, Buegeleisen M, Tusie-Luna MT, Lesser M, New MI, White PC. Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Invest. 1992 Aug; 90(2):584-95.
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    174. Schram P, Zerah M, Mani P, Jewelewicz R, Jaffe S, New MI. Nonclassical 3 beta-hydroxysteroid dehydrogenase deficiency: a review of our experience with 25 female patients. Fertil Steril. 1992 Jul; 58(1):129-36.
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    175. Rhéaume E, Simard J, Morel Y, Mebarki F, Zachmann M, Forest MG, New MI, Labrie F. Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene. Nat Genet. 1992 Jul; 1(4):239-45.
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    176. Speiser PW, New MI, Tannin GM, Pickering D, Yang SY, White PC. Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Genet. 1992 Mar; 88(6):647-8.
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    177. Karaviti LP, Mercado AB, Mercado MB, Speiser PW, Buegeleisen M, Crawford C, Antonian L, White PC, New MI. Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia). J Steroid Biochem Mol Biol. 1992 Mar; 41(3-8):445-51.
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    178. Vellodi A, Young E, New M, Pot-Mees C, Hugh-Jones K. Bone marrow transplantation for Sanfilippo disease type B. J Inherit Metab Dis. 1992; 15(6):911-8.
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    179. New MI. Genetic disorders of adrenal hormone synthesis. Horm Res. 1992; 37 Suppl 3:22-33.
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    180. White PC, New MI. Genetic basis of endocrine disease 2: congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Endocrinol Metab. 1992 Jan; 74(1):6-11.
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    181. Tannin GM, Agarwal AK, Monder C, New MI, White PC. The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization. J Biol Chem. 1991 Sep 5; 266(25):16653-8.
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    182. New MI. Replacement doses of glucocorticoids. J Pediatr. 1991 Jul; 119(1 Pt 1):161.
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    183. White PC, Dupont J, New MI, Leiberman E, Hochberg Z, Rösler A. A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin. J Clin Invest. 1991 May; 87(5):1664-7.
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    184. Tusie-Luna MT, Speiser PW, Dumic M, New MI, White PC. A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele. Mol Endocrinol. 1991 May; 5(5):685-92.
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    185. Speiser PW, Agdere L, Ueshiba H, White PC, New MI. Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase. N Engl J Med. 1991 Jan 17; 324(3):145-9.
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    186. Harbison MD, Magid ML, Josso N, Mininberg DT, New MI. Anti-Müllerian hormone in three intersex conditions. Ann Genet. 1991; 34(3-4):226-32.
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    187. New MI. The Gordon Wilson Lecture. Congenital adrenal hyperplasia. Trans Am Clin Climatol Assoc. 1991; 102:108-22.
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    188. Ulick S, Chan CK, Gill JR, Gutkin M, Letcher L, Mantero F, New MI. Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronism. J Clin Endocrinol Metab. 1990 Nov; 71(5):1151-7.
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    189. Lorberboym M, Sarkar SD, Speiser P, Tannen G, New MI. Bilateral adrenal uptake of gallium-67 citrate in a patient with congenital adrenal hyperplasia. Clin Nucl Med. 1990 Nov; 15(11):849.
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    190. Zerah M, Ueshiba H, Wood E, Speiser PW, Crawford C, McDonald T, Pareira J, Gruen D, New MI. Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample study. J Clin Endocrinol Metab. 1990 Jun; 70(6):1662-7.
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    191. New MI. Prenatal diagnosis and treatment of adrenogenital syndrome (steroid 21-hydroxylase deficiency). Dev Pharmacol Ther. 1990; 15(3-4):200-10.
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    192. Kessler DB, New MI. Emerging trends in child abuse and neglect. Pediatr Ann. 1989 Aug; 18(8):471-2, 474-5.
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    193. Marteau TM, Johnston M, Shaw RW, Michie S, Kidd J, New M. The impact of prenatal screening and diagnostic testing upon the cognitions, emotions and behaviour of pregnant women. J Psychosom Res. 1989; 33(1):7-16.
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    194. New MI, Gertner JM, Speiser PW, Del Balzo P. Growth and final height in classical and nonclassical 21-hydroxylase deficiency. J Endocrinol Invest. 1989; 12(8 Suppl 3):91-5.
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    195. Speiser PW, New MI, White PC. Clinical and genetic characterization of nonclassic 21-hydroxylase deficiency. Endocr Res. 1989; 15(1-2):257-76.
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    196. New MI. Polycystic ovarian disease and congenital and late-onset adrenal hyperplasia. Endocrinol Metab Clin North Am. 1988 Dec; 17(4):637-48.
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    197. Globerman H, Rösler A, Theodor R, New MI, White PC. An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylase. N Engl J Med. 1988 Nov 3; 319(18):1193-7.
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    198. White PC, New MI. Molecular genetics of congenital adrenal hyperplasia. Baillieres Clin Endocrinol Metab. 1988 Nov; 2(4):941-65.
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    199. New M. Congenital adrenal hyperplasia. Biochem Soc Trans. 1988 Oct; 16(5):691-4.
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    200. Aston CE, Sherman SL, Morton NE, Speiser PW, New MI. Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies. Am J Hum Genet. 1988 Sep; 43(3):304-10.
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    201. Speiser PW, New MI, White PC. Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1. N Engl J Med. 1988 Jul 7; 319(1):19-23.
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    202. Globerman H, Amor M, Parker KL, New MI, White PC. Nonsense mutation causing steroid 21-hydroxylase deficiency. J Clin Invest. 1988 Jul; 82(1):139-44.
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    203. New MI, Brown P, Temeck JW, Owens C, Hedley-Whyte ET, Richardson EP. Preclinical Creutzfeldt-Jakob disease discovered at autopsy in a human growth hormone recipient. Neurology. 1988 Jul; 38(7):1133-4.
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    204. New MI, Josso N. Disorders of gonadal differentiation and congenital adrenal hyperplasia. Endocrinol Metab Clin North Am. 1988 Jun; 17(2):339-66.
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    205. Sherman SL, Aston CE, Morton NE, Speiser PW, New MI. A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency. Am J Hum Genet. 1988 Jun; 42(6):830-8.
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    206. White PC, Vitek A, Dupont B, New MI. Characterization of frequent deletions causing steroid 21-hydroxylase deficiency. Proc Natl Acad Sci U S A. 1988 Jun; 85(12):4436-40.
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    207. Amor M, Parker KL, Globerman H, New MI, White PC. Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency. Proc Natl Acad Sci U S A. 1988 Mar; 85(5):1600-4.
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    208. Britton H, Shehab Z, Lightner E, New M, Chow D. Adrenal response in children receiving high doses of ketoconazole for systemic coccidioidomycosis. J Pediatr. 1988 Mar; 112(3):488-92.
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    209. Sasano H, White PC, New MI, Sasano N. Immunohistochemical localization of cytochrome P-450C21 in human adrenal cortex and its relation to endocrine function. Hum Pathol. 1988 Feb; 19(2):181-5.
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    210. New MI, Gertner JM, Speiser PW, del Balzo P. Growth and final height in classical and nonclassical 21-hydroxylase deficiency. Acta Paediatr Jpn. 1988; 30 Suppl:79-88.
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    211. Sasano H, White PC, New MI, Sasano N. Immunohistochemistry of cytochrome P-450 21-hydroxylase: microscopic examination of the enzyme in the bovine adrenal cortex and kidney. Endocrinology. 1988 Jan; 122(1):291-5.
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    212. Pang SY, Legido A, Levine LS, Temeck JW, New MI. Adrenal androgen response to metyrapone, adrenocorticotropin, and corticotropin-releasing hormone stimulation in children with hypopituitarism. J Clin Endocrinol Metab. 1987 Aug; 65(2):282-9.
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    213. Drucker S, New MI. Nonclassic adrenal hyperplasia due to 21-hydroxylase deficiency. Pediatr Clin North Am. 1987 Aug; 34(4):1067-81.
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    214. Drucker S, New MI. Disorders of adrenal steroidogenesis. Pediatr Clin North Am. 1987 Aug; 34(4):1055-66.
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    215. Zerah M, Pang SY, New MI. Morning salivary 17-hydroxyprogesterone is a useful screening test for nonclassical 21-hydroxylase deficiency. J Clin Endocrinol Metab. 1987 Aug; 65(2):227-32.
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    216. DiMartino-Nardi J, Stoner E, Martin K, Balfe JW, Jose PA, New MI. New findings in apparent mineralocorticoid excess. Clin Endocrinol (Oxf). 1987 Jul; 27(1):49-62.
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    217. Cappa M, Stoner E, DiMartino-Nardi J, Pang S, Temeck J, New MI. Recurrence of Cushing's disease in childhood after radiotherapy-induced remission. Am J Dis Child. 1987 Jul; 141(7):736-40.
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    218. White PC, New MI, Dupont B. Congenital adrenal hyperplasia (2). N Engl J Med. 1987 Jun 18; 316(25):1580-6.
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    219. White PC, New MI, Dupont B. Congenital adrenal hyperplasia. (1). N Engl J Med. 1987 Jun 11; 316(24):1519-24.
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    220. Pang SY, Softness B, Sweeney WJ, New MI. Hirsutism, polycystic ovarian disease, and ovarian 17-ketosteroid reductase deficiency. N Engl J Med. 1987 May 21; 316(21):1295-301.
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    221. Anderson KE, Rosner W, Khan MS, New MI, Pang SY, Wissel PS, Kappas A. Diet-hormone interactions: protein/carbohydrate ratio alters reciprocally the plasma levels of testosterone and cortisol and their respective binding globulins in man. Life Sci. 1987 May 4; 40(18):1761-8.
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    222. Nass R, Baker S, Speiser P, Virdis R, Balsamo A, Cacciari E, Loche A, Dumic M, New M. Hormones and handedness: left-hand bias in female congenital adrenal hyperplasia patients. Neurology. 1987 Apr; 37(4):711-5.
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    223. Lahita RG, Bradlow HL, Ginzler E, Pang S, New M. Low plasma androgens in women with systemic lupus erythematosus. Arthritis Rheum. 1987 Mar; 30(3):241-8.
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    224. Temeck JW, Pang SY, Nelson C, New MI. Genetic defects of steroidogenesis in premature pubarche. J Clin Endocrinol Metab. 1987 Mar; 64(3):609-17.
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    225. New MI. Basic and clinical aspects of congenital adrenal hyperplasia. J Steroid Biochem. 1987; 27(1-3):1-7.
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    226. Speiser PW, New MI. Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency. J Clin Endocrinol Metab. 1987 Jan; 64(1):86-91.
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    227. DiMartino-Nardi J, New MI. Low-renin hypertension of childhood. Pediatr Nephrol. 1987 Jan; 1(1):99-108.
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    228. Werkmeister JW, New MI, Dupont B, White PC. Frequent deletion and duplication of the steroid 21-hydroxylase genes. Am J Hum Genet. 1986 Oct; 39(4):461-9.
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    229. Loche S, Rifkind AB, Stoner E, Conney AH, New MI. Antipyrine clearance in congenital adrenal hyperplasia. Clin Endocrinol (Oxf). 1986 Sep; 25(3):233-9.
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    230. Monder C, Shackleton CH, Bradlow HL, New MI, Stoner E, Iohan F, Lakshmi V. The syndrome of apparent mineralocorticoid excess: its association with 11 beta-dehydrogenase and 5 beta-reductase deficiency and some consequences for corticosteroid metabolism. J Clin Endocrinol Metab. 1986 Sep; 63(3):550-7.
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    231. New MI, Speiser PW. Genetics of adrenal steroid 21-hydroxylase deficiency. Endocr Rev. 1986 Aug; 7(3):331-49.
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    232. Nass R, Engel M, Stoner E, Pang S, New MI. Empty sella syndrome in childhood. Pediatr Neurol. 1986 Jul-Aug; 2(4):224-9.
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    233. White PC, New MI, Dupont B. Structure of human steroid 21-hydroxylase genes. Proc Natl Acad Sci U S A. 1986 Jul; 83(14):5111-5.
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    234. White PC, Werkmeister J, New MI, Dupont B. Steroid 21-hydroxylase deficiency and the major histocompatibility complex. Hum Immunol. 1986 Apr; 15(4):404-15.
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    235. Nass R, Petito C, Stoner E, New M. Neuronal ceroid lipofuscinosis with hypergonadotropic hypogonadism. J Child Neurol. 1986 Apr; 1(2):142-4.
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    236. Ludvigsson J, Samuelsson U, Beauforts C, Deschamps I, Dorchy H, Drash A, Francois R, Herz G, New M, Schober E. HLA-DR 3 is associated with a more slowly progressive form of type 1 (insulin-dependent) diabetes. Diabetologia. 1986 Apr; 29(4):207-10.
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    237. Oberfield SE, Allen JC, Pollack J, New MI, Levine LS. Long-term endocrine sequelae after treatment of medulloblastoma: prospective study of growth and thyroid function. J Pediatr. 1986 Feb; 108(2):219-23.
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    238. Stoner E, Loche S, Mirth A, New MI. Clinical utility of adrenal steroid measurement by high-performance liquid chromatography in pediatric endocrinology. J Chromatogr. 1986 Jan 24; 374(2):358-62.
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    239. New MI, Stoner E, DiMartino-Nardi J. Apparent mineralocorticoid excess causing hypertension and hypokalemia in children. Clin Exp Hypertens A. 1986; 8(4-5):751-72.
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    240. DiMartino-Nardi J, Stoner E, O'Connell A, New MI. The effect of treatment of final height in classical congenital adrenal hyperplasia (CAH). Acta Endocrinol Suppl (Copenh). 1986; 279:305-14.
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    241. Stoner E, Dimartino-Nardi J, Kuhnle U, Levine LS, Oberfield SE, New MI. Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect? Clin Endocrinol (Oxf). 1986 Jan; 24(1):9-20.
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    242. New MI. Molecular genetics and the characterization of steroid 21-hydroxylase deficiency. Endocr Res. 1986; 12(4):505-22.
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    243. Fallo F, Oberfield SE, Levine LS, Stoner E, Greig F, Sniderman K, Saddekni S, Sos T, New MI. Percutaneous transluminal renal angioplasty in the treatment of renovascular hypertension in children. Clin Exp Hypertens A. 1986; 8(4-5):887-91.
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    244. Speiser PW, Stoner E, New MI. Pseudohypoaldosteronism: a review and report of two new cases. Adv Exp Med Biol. 1986; 196:173-95.
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    245. Loche S, Rifkind AB, Stoner E, Faedda A, Garabedian MC, New MI. Microfilter paper method for antipyrine determination in whole blood by high pressure liquid chromatography. Ther Drug Monit. 1986; 8(2):214-8.
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    246. Van Thiel DH, Gartner LM, Thorp FK, Newman SL, Lindahl JA, Stoner E, New MI, Starzl TE. Resolution of the clinical features of tyrosinemia following orthotopic liver transplantation for hepatoma. J Hepatol. 1986; 3(1):42-8.
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    247. White PC, New MI, Dupont B. Adrenal 21-hydroxylase cytochrome P-450 genes within the MHC class III region. Immunol Rev. 1985 Oct; 87:123-50.
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    248. Fallo F, Oberfield SE, Levine LS, Stoner E, Greig F, New MI, Sniderman K, Saddekni S, Sos T. Evaluation of percutaneous transluminal renal angioplasty in childhood hypertension. Int J Pediatr Nephrol. 1985 Oct-Dec; 6(4):261-6.
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    249. Speiser PW, Martin KO, Kao-Lo G, New MI. Excess mineralocorticoid receptor activity in patients with dexamethasone-suppressible hyperaldosteronism is under adrenocorticotropin control. J Clin Endocrinol Metab. 1985 Aug; 61(2):297-302.
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    250. Meyer-Bahlburg HF, Ehrhardt AA, Bell JJ, Cohen SF, Healey JM, Feldman JF, Morishima A, Baker SW, New MI. Idiopathic precocious puberty in girls: Psychosexual development. J Youth Adolesc. 1985 Aug; 14(4):339-53.
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    251. Ghizzoni L, Muller-Eberhard U, Liem HH, New M, Finlayson M, Johnson EF. Characterization of variations in rabbit hepatic progesterone 21-hydroxylase activity by serial biopsy. Biochem Biophys Res Commun. 1985 Jul 16; 130(1):43-9.
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    252. Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1985 Jul; 61(1):89-97.
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    253. Speiser PW, Dupont B, Rubinstein P, Piazza A, Kastelan A, New MI. High frequency of nonclassical steroid 21-hydroxylase deficiency. Am J Hum Genet. 1985 Jul; 37(4):650-67.
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    254. Pang SY, Lerner AJ, Stoner E, Levine LS, Oberfield SE, Engel I, New MI. Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women. J Clin Endocrinol Metab. 1985 Mar; 60(3):428-39.
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    255. White PC, Grossberger D, Onufer BJ, Chaplin DD, New MI, Dupont B, Strominger JL. Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man. Proc Natl Acad Sci U S A. 1985 Feb; 82(4):1089-93.
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    256. New MI. Genetics of congenital adrenal hyperplasia. Prog Clin Biol Res. 1985; 200:233-41.
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    257. Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia. Ann N Y Acad Sci. 1985; 458:111-29.
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    258. White PC, New MI, Dupont B. Molecular cloning of steroid 21-hydroxylase. Ann N Y Acad Sci. 1985; 458:277-87.
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    259. Pang S, Spence DA, New MI. Newborn screening for congenital adrenal hyperplasia with special reference to screening in Alaska. Ann N Y Acad Sci. 1985; 458:90-102.
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    260. New MI. Clinical and endocrinological aspects of 21-hydroxylase deficiency. Ann N Y Acad Sci. 1985; 458:1-27.
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    261. Muller-Eberhard U, Ghizzoni L, Liem HH, New M, Finlayson M, Johnson EF. Evidence that variation among untreated rabbits in hepatic progesterone 21-hydroxylase activity is indicative of enzyme heterogeneity rather than a transient inductive effect. Ann N Y Acad Sci. 1985; 458:225-31.
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    262. Loche S, Porcelli F, Rosen M, Feffer M, Stoner E, New MI. Clinical applications of the rapid high-performance liquid chromatographic determination of serum cortisol. J Chromatogr. 1984 Dec 28; 317:377-82.
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    263. Stoner E, Starkman H, Wellner D, Wellner VP, Sassa S, Rifkind AB, Grenier A, Steinherz PG, Meister A, New MI, et al. Biochemical studies of a patient with hereditary hepatorenal tyrosinemia: evidence of glutathione deficiency. Pediatr Res. 1984 Dec; 18(12):1332-6.
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    264. White PC, New MI, Dupont B. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation. Proc Natl Acad Sci U S A. 1984 Dec; 81(23):7505-9.
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    265. White PC, Chaplin DD, Weis JH, Dupont B, New MI, Seidman JG. Two steroid 21-hydroxylase genes are located in the murine S region. Nature. 1984 Nov 29-Dec 5; 312(5993):465-7.
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    266. New MI, Pang S. Polycystic ovary syndrome and congenital adrenal hyperplasia. Clin Endocrinol (Oxf). 1984 Jun; 20(6):733-4.
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    267. Greig F, Oberfield SE, Levine LS, Ghavimi F, Pang S, New MI. Recovery of adrenal function after treatment of adrenocortical carcinoma with o,p'-DDD. Clin Endocrinol (Oxf). 1984 Apr; 20(4):389-99.
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    268. White PC, New MI, Dupont B. Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation. Proc Natl Acad Sci U S A. 1984 Apr; 81(7):1986-90.
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    269. Stiehm ER, DeVivo DC, Brann AW, Fisher DA, Hodson WA, New MI, Shearer WT, Sokol RJ, Sunshine P, Taeusch HW. Advances in perinatology from the clinical research centers. Pediatr Res. 1984 Feb; 18(2):197-212.
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    270. Oberfield SE, Levine LS, Firpo A, Lawrence D, Stoner E, Levy DJ, Sen S, New MI. Primary hyperaldosteronism in childhood due to unilateral macronodular hyperplasia. Case report. Hypertension. 1984 Jan-Feb; 6(1):75-84.
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    271. White PC, Dupont B, New MI. Molecular cloning of steroid 21-hydroxylase. Endocr Res. 1984-1985; 10(3-4):335-45.
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    272. New MI, Levine LS. Recent advances in 21-hydroxylase deficiency. Annu Rev Med. 1984; 35:649-63.
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    273. New MI, Levine LS. Congenital adrenal hyperplasia. Monogr Endocrinol. 1984; 26:1-88.
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    274. Ehrhardt AA, Meyer-Bahlburg HF, Bell JJ, Cohen SF, Healey JM, Stiel R, Feldman JF, Morishima A, New MI. Idiopathic precocious puberty in girls: psychiatric follow-up in adolescence. J Am Acad Child Psychiatry. 1984 Jan; 23(1):23-33.
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    275. New MI, Lorenzen F, Lerner AJ, Kohn B, Oberfield SE, Pollack MS, Dupont B, Stoner E, Levy DJ, Pang S, Levine LS. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data. J Clin Endocrinol Metab. 1983 Aug; 57(2):320-6.
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    276. Curtis JA, Monaghan HP, New MI, Bailey JD. Selective hypoaldosteronism in infancy. Report of a case. Am J Dis Child. 1983 Jul; 137(7):633-6.
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    277. Kuhnle U, Rösler A, Pareira JA, Gunzcler P, Levine LS, New MI. The effects of long-term normalization of sodium balance on linear growth in disorders with aldosterone deficiency. Acta Endocrinol (Copenh). 1983 Apr; 102(4):577-82.
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    278. Mandel FP, Chang RJ, Dupont B, Pollack MS, Levine LS, New MI, Lu JK, Judd HL. HLA genotyping in family members and patients with familial polycystic ovarian disease. J Clin Endocrinol Metab. 1983 Apr; 56(4):862-4.
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    279. Pang S, Levine LS, Stoner E, Opitz JM, Pollack MS, Dupont B, New MI. Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa function. J Clin Endocrinol Metab. 1983 Apr; 56(4):808-18.
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    280. Sen S, Bumpus FM, Oberfield S, New MI. Development and preliminary application of a new assay for aldosterone stimulating factor. Hypertension. 1983 Mar-Apr; 5(2 Pt 2):I27-31.
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    281. Virdis R, Levine LS, Levy D, Pang S, Rapaport R, New MI. Congenital adrenal hypoplasia: two new cases. J Endocrinol Invest. 1983 Feb; 6(1):51-4.
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    282. Oberfield SE, Levine LS, Carey RM, Greig F, Ulick S, New MI. Metabolic and blood pressure responses to hydrocortisone in the syndrome of apparent mineralocorticoid excess. J Clin Endocrinol Metab. 1983 Feb; 56(2):332-9.
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    283. Kohn B, Levine LS, Pollack MS, Pang S, Lorenzen F, Levy D, Lerner AJ, Rondanini GF, Dupont B, New MI. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1982 Nov; 55(5):817-27.
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    284. Pang S, Murphey W, Levine LS, Spence DA, Leon A, LaFranchi S, Surve AS, New MI. A pilot newborn screening for congenital adrenal hyperplasia in Alaska. J Clin Endocrinol Metab. 1982 Sep; 55(3):413-20.
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    285. Oberfield SE, Rapaport R, Levine LS, New MI. Long-term treatment of childhood hypertension with captopril. Pediatr Ann. 1982 Jul; 11(7):614-6, 620-1.
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    286. Oberfield SE, Levine LS, New MI. Childhood hypertension due to adrenocortical disorders. Pediatr Ann. 1982 Jul; 11(7):623-6, 628.
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    287. O'Neill GJ, Dupont B, Pollack MS, Levine LS, New MI. Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus. Clin Immunol Immunopathol. 1982 May; 23(2):312-22.
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    288. Saenger P, Levine LS, Irvine WJ, Gottesdiener K, Rauh W, Sonino N, Chow D, New MI. Progressive adrenal failure in polyglandular autoimmune disease. J Clin Endocrinol Metab. 1982 Apr; 54(4):863-7.
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    289. Lee SM, Lightner E, Witte M, Oberfield S, Levine L, New MI. Dexamethasone suppressible hyperaldosteronism in a child with nephrosclerosis. Acta Endocrinol (Copenh). 1982 Feb; 99(2):251-5.
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    290. Teitelman G, Joh TH, Park D, Brodsky M, New M, Reis DJ. Expression of the adrenergic phenotype in cultured fetal adrenal medullary cells: role of intrinsic and extrinsic factors. Dev Biol. 1982 Feb; 89(2):450-9.
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    291. Mininberg DT, Levine LS, New MI. Current concepts in congenital adrenal hyperplasia. Pathol Annu. 1982; 17 Pt 2:179-95.
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    292. Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency. J Clin Endocrinol Metab. 1981 Dec; 53(6):1193-8.
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    293. New MI, Levine LS. Congenital adrenal hyperplasia. Clin Biochem. 1981 Oct; 14(5):258-72.
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    294. Sonino N, Levine LS, New MI. Mineralocorticoid and metabolic response to metyrapone on normotensive children and children with dexamethasone-suppressible and primary hyperaldosteronism. Acta Endocrinol (Copenh). 1981 Sep; 98(1):87-94.
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    295. Rifkind AB, Saenger P, Levine LS, Pareira J, New MI. Effects of growth hormone on antipyrine kinetics in children. Clin Pharmacol Ther. 1981 Jul; 30(1):127-32.
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    296. Pollack MS, Levine LS, O'Neill GJ, Pang S, Lorenzen F, Kohn B, Rondanini GF, Chiumello G, New MI, Dupont B. HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency. Am J Hum Genet. 1981 Jul; 33(4):540-50.
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    297. Oberfield SE, Levine LS, Stoner E, Chow D, Rauh W, Greig F, Lee SM, Lightner E, Witte M, New MI. Adrenal glomerulosa function in patients with dexamethasone-suppressible hyperaldosteronism. J Clin Endocrinol Metab. 1981 Jul; 53(1):158-64.
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    298. Rapaport R, Levine LS, Petrovic M, Wilson T, Draznin M, Bejar RL, Johanson A, New MI. The renin-aldosterone system in cystic fibrosis. J Pediatr. 1981 May; 98(5):768-71.
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    299. Newman CB, Levine LS, New MI. Endocrine function in children with intrasellar and suprasellar neoplasms: before and after therapy. Am J Dis Child. 1981 Mar; 135(3):259-66.
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    300. Kuhnle U, Chow D, Rapaport R, Pang S, Levine LS, New MI. The 21-hydroxylase activity in the glomerulosa and fasciculata of the adrenal cortex in congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1981 Mar; 52(3):534-44.
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    301. Pollack MS, New MI, O'Neill GJ, Levine LS, Callaway C, Pang S, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, Dupont B. HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency. Hum Genet. 1981; 58(3):331-7.
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    302. New MI, Dupont B, Pollack MS, Levine LS. The biochemical basis for genotyping 21-hydroxylase deficiency. Hum Genet. 1981; 58(1):123-7.
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    303. New MI, Dupont B, Pang S, Pollack M, Levine LS. An update of congenital adrenal hyperplasia. Recent Prog Horm Res. 1981; 37:105-81.
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    304. Sonino N, Chow D, Levine LS, New MI. Clinical response to metyrapone as indicated by measurement of mineralocorticoids and glucocorticoids in normal children. Clin Endocrinol (Oxf). 1981 Jan; 14(1):31-9.
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    305. Oberfield SE, Levine LS, Wellner D, Novogroder M, Laino P, New MI. Ascorbic acid treatment in nephropathic cystinosis in identical twins. Dev Pharmacol Ther. 1981; 2(2):80-90.
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    306. Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1980 Dec; 51(6):1316-24.
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    307. Ferraris J, Saenger P, Levine L, New M, Pang S, Saxena BB, Lewy JE. Delayed puberty in males with chronic renal failure. Kidney Int. 1980 Sep; 18(3):344-50.
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    308. Sonino N, Levine LS, Vecsei P, New MI. Parallelism of 11 beta- and 18-hydroxylation demonstrated by urinary free hormones in man. J Clin Endocrinol Metab. 1980 Sep; 51(3):557-60.
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    309. Rauh W, Gottesdiener K, Chow D, Forster E, Saenger P, Levine LS, New MI. Aldosterone response to prolonged ACTH infusion in juvenile hypertension. Pediatr Res. 1980 Sep; 14(9):1035-9.
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    310. Pang S, Levine LS, Cederqvist LL, Fuentes M, Riccardi VM, Holcombe JH, Nitowsky HM, Sachs G, Anderson CE, Duchon MA, Owens R, Merkatz I, New MI. Amniotic fluid concentrations of delta 5 and delta 4 steroids in fetuses with congenital adrenal hyperplasia due to 21 hydroxylase deficiency and in anencephalic fetuses. J Clin Endocrinol Metab. 1980 Aug; 51(2):223-9.
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    311. Laron Z, Pollack MS, Zamir R, Roitman A, Dickerman Z, Levine LS, Lorenzen F, O'Neill GJ, Pang S, New MI, Dupont B. Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus. Hum Immunol. 1980 Jul; 1(1):55-66.
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    312. Lan NC, Matulich DT, Stockigt JR, Biglieri EG, New MI, Winter JS, McKenzie JK, Baxter JD. Radioreceptor assay of plasma mineralocorticoid activity. Role of aldosterone, cortisol, and deoxycorticosterone in various mineralocorticoid-excess states. Circ Res. 1980 Jun; 46(6 Pt 2):I94-100.
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    313. Pang S, Shine S, Levine LS, New MI. Practical advances in cortisol and dehydroepiandrosterone sulfate radioimmunoassay using the microfilter paper method. J Lab Clin Med. 1980 Apr; 95(4):515-24.
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    314. Levine LS, Pang S, Dupont B, Pollack M, Lorenzen F, New MI. Detection of heterozygote of 21-hydroxylase deficiency. Lancet. 1980 Mar 15; 1(8168 Pt 1):603-4.
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    315. New MI, Oberfield SE, Levine LS, Dupont B, Pollack M, Gill JR, Bartter FC. Autosomal dominant transmission and absence of HLA linkage in dexamethasone suppressible hyperaldosteronism. Lancet. 1980 Mar 8; 1(8167):550-1.
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    316. Lorenzen F, Pang S, New M, Pollack M, Oberfield S, Dupont B, Chow D, Schneider B, Levine L. Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Endocrinol Metab. 1980 Mar; 50(3):572-7.
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    317. Pang S, Levine LS, Lorenzen F, Chow D, Pollack M, Dupont B, Genel M, New MI. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1980 Mar; 50(3):586-9.
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    318. Saenger P, Schwartz E, Markenson AL, Graziano JH, Levine LS, New MI, Hilgartner MW. Depressed serum somatomedin activity in beta-thalassemia. J Pediatr. 1980 Feb; 96(2):214-8.
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    319. Levine LS, Rauh W, Gottesdiener K, Chow D, Gunczler P, Rapaport R, Pang S, Schneider B, New MI. New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1980 Feb; 50(2):258-63.
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    320. New MI, Levine LS. Hypertension of childhood with suppressed renin. Endocr Rev. 1980; 1(4):421-30.
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    321. New MI, Levine LS. Low-renin hypertension with hyperaldosteronism in childhood. Prog Biochem Pharmacol. 1980; 17:54-7.
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    322. Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon MA, Owens RP, Merkatz IR, Nitowsky HM, Sachs G, Dupont B. HLA typing of amniotic cells: the prenatal diagnosis of congenital adrenal hyperplasia (21-OH-deficiency type). Transplant Proc. 1979 Dec; 11(4):1726-8.
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    323. Pang S, Levine LS, Chow DM, Faiman C, New MI. Serum androgen concentrations in neonates and young infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clin Endocrinol (Oxf). 1979 Dec; 11(6):575-84.
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    324. Lorenzen F, Pang S, New MI, Dupont B, Pollack M, Chow DM, Levine LS. Hormonal phenotype and HLA-genotype in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). Pediatr Res. 1979 Dec; 13(12):1356-60.
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    325. O'Neill GJ, Pollack MS, Yang SY, Levine LS, New MI, Dupont B. Gene frequencies and genetic linkage disequilibrium for the HLA-linked genes Bf, C2, C4S, C4F, 21-hydroxylase deficiency, and glyoxalase I. Transplant Proc. 1979 Dec; 11(4):1713-5.
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    326. Ulick S, Levine LS, Gunczler P, Zanconato G, Ramirez LC, Rauh W, Rösler A, Bradlow HL, New MI. A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol. J Clin Endocrinol Metab. 1979 Nov; 49(5):757-64.
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    327. Mininberg DT, Levine LS, New MI. Current concepts in congenital adrenal hyperplasia. Invest Urol. 1979 Nov; 17(3):169-75.
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    328. Oberfield SE, Case DB, Levine LS, Rapaport R, Rauh W, New MI. Use of the oral angiotensin I--converting enzyme inhibitor (captopril) in childhood malignant hypertension. J Pediatr. 1979 Oct; 95(4):641-4.
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    329. Levine LS, New MI, Pollack M, Dupont B. Prenatal diagnosis of congenital adrenal hyperplasia. Lancet. 1979 Sep 22; 2(8143):637.
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    330. Rauh W, Levine LS, Gottesdiener K, Chow D, Oberfield SE, Gunczler P, Pareira J, New MI. Adrenocortical function, electrolyte metabolism, and blood pressure during prolonged adrenocorticotropin infusion in juvenile hypertension. J Clin Endocrinol Metab. 1979 Jul; 49(1):52-7.
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    331. McVie R, Levine LS, New MI. The biologic significance of the aldosterone concentration in saliva. Pediatr Res. 1979 Jun; 13(6):755-9.
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    332. Pollack MS, Levine L, Zachmann M, Prader A, New M, Oberfield S, Dupont B. Possible genetic linkage disequilibrium between HLA and the 21-hydroxylase deficiency gene (congenital adrenal hyperplasia). Transplant Proc. 1979 Jun; 11(2):1315-6.
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    333. Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon M, Owens RP, Merkatz IR, Nitowsky BM, Sachs G, Dupont B. Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing. Lancet. 1979 May 26; 1(8126):1107-8.
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    334. Pang S, Levine LS, Chow D, Sagiani F, Saenger P, New MI. Dihydrotestosterone and its relationship to testosterone in infancy and childhood. J Clin Endocrinol Metab. 1979 May; 48(5):821-6.
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    335. Loggie JM, New MI, Robson AM. Hypertension in the pediatric patient: a reappraisal. J Pediatr. 1979 May; 94(5):685-99.
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    336. Voccia E, Saenger P, Peterson RE, Rauh W, Gottesdiener K, Levine LS, New MI. 6 beta-Hydroxycortisol excretion in hypercortisolemic states. J Clin Endocrinol Metab. 1979 Mar; 48(3):467-71.
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    337. New MI, Lorenzen F, Pang S, Gunczler P, Dupont B, Levine LS. "Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1979 Feb; 48(2):356-9.
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    338. Oberfield SE, Levine LS, Carey RM, Bejar R, New MI. Pseudohypoaldosteronism: multiple target organ unresponsiveness to mineralocorticoid hormones. J Clin Endocrinol Metab. 1979 Feb; 48(2):228-34.
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    339. Brautbar C, Rösler A, Landau H, Cohen I, Nelken D, Cohen T, Levine C, Sack J, Benderli A, Moses S, Lieberman E, Dupont B, Levine LS, New MI. No linkage between HLA and congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency. N Engl J Med. 1979 Jan 25; 300(4):205-6.
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    340. Yang SY, Levine LS, Zachmann M, New MI, Prader A, Oberfield SE, O'Neill GJ, Pollack MS, Dupont B. Mapping of the 21-hydroxylase deficiency gene within the HLA linkage group. Transplant Proc. 1978 Dec; 10(4):753-5.
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    341. Levine LS, Zachmann M, New MI, Prader A, Pollack MS, O'Neill GJ, Yang SY, Oberfield SE, Dupont B. Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group. N Engl J Med. 1978 Oct 26; 299(17):911-5.
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    342. Levine LS, Novogroder M, Saxena B, Saenger P, Saito T, New MI. Primary intracranial HCG-producing germinoma in a boy with congenital adrenal hyperplasia. Acta Endocrinol (Copenh). 1978 May; 88(1):122-31.
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    343. Saenger P, Goldman AS, Levine LS, Korth-Schutz S, Muecke EC, Katsumata M, Doberne Y, New MI. Prepubertal diagnosis of steroid 5 alpha-reductase deficiency. J Clin Endocrinol Metab. 1978 Apr; 46(4):627-34.
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    344. Korth-Schutz S, Virdis R, Saenger P, Chow DM, Levine LS, New MI. Serum androgens as a continuing index of adequacy of treatment of congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1978 Mar; 46(3):452-8.
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    345. New MI, Levine LS. Adrenocortical hypertension. Pediatr Clin North Am. 1978 Feb; 25(1):67-81.
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    346. Virdis R, Saenger P, Senior B, New MI. Endocrine studies in a pubertal male pseudohermaphrodite with 17-ketosteroid reductase deficiency. Acta Endocrinol (Copenh). 1978 Jan; 87(1):212-24.
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    347. Rauh W, Levine LS, Gottesdiener K, New MI. Mineralocorticoids, salt balance and blood pressure after prolonged ACTH administration in juvenile hypertension. Klin Wochenschr. 1978; 56 Suppl 1:161-7.
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    348. Pang S, Hotchkiss J, Drash AL, Levine LS, New MI. Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1977 Nov; 45(5):1003-8.
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    349. Rösler A, Levine LS, Schneider B, Novogroder M, New MI. The interrelationship of sodium balance, plasma renin activity and ACTH in congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1977 Sep; 45(3):500-12.
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    350. Saenger P, New M. Inhibitory action of dehydroepiandrosterone (DHEA) on fibroblast growth. Experientia. 1977 Jul 15; 33(7):966-7.
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    351. Koo GC, Wachtel SS, Saenger P, New MI, Dosik H, Amarose AP, Dorus E, Ventruto V. H-y antigen: expression in human subjects with the testicular feminization syndrome. Science. 1977 May 6; 196(4290):655-6.
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    352. New MI, Levine LS. Mineralocorticoid hypertension in childhood. Mayo Clin Proc. 1977 May; 52(5):323-8.
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    353. New MI, Levine LS, Biglieri EG, Pareira J, Ulick S. Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension. J Clin Endocrinol Metab. 1977 May; 44(5):924-33.
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    354. Ulick S, Ramirez LC, New MI. An abnormality in steroid reductive metabolism in a hypertensive syndrome. J Clin Endocrinol Metab. 1977 Apr; 44(4):799-802.
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    355. Korth-Schutz S, Levine LS, Roth JA, Saenger P, New MI. Virilizing adrenal tumor in a child suppressed with dexamethasone for three years. Effect of o,p'-DDD on serum and urinary androgens. J Clin Endocrinol Metab. 1977 Mar; 44(3):433-9.
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    356. Saenger P, Levine LS, Wiedemann E, Schwartz E, Korth-Schutz S, Pareira J, Heinig B, New MI. Somatomedin and growth hormone in psychosocial dwarfism. Padiatr Padol Suppl. 1977; (5):1-12.
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    357. Saenger P, Levine LS, Wachtel SS, Korth-Schutz S, Doberne Y, Koo GC, Lavengood RW, German JL, New MI. Presence of H-Y antigen and testis in 46, XX true hermaphroditism, evidence for Y-chromosomal function. J Clin Endocrinol Metab. 1976 Dec; 43(6):1234-9.
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    358. New MI, Peterson RE, Saenger P, Levine LS. Evidence for an unidentified ACTH-induced steroid hormone causing hypertension. J Clin Endocrinol Metab. 1976 Dec; 43(6):1283-93.
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    359. Rifkind AB, Canale V, New MI. Antipyrin clearance in homozygous beta-thalassemia. Clin Pharmacol Ther. 1976 Oct; 20(4):476-83.
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    360. Wachtel SS, Koo GC, Breg WR, Thaler HT, Dillard GM, Rosenthal IM, Dosik H, Gerald PS, Saenger P, New M, Lieber E, Miller OJ. Serologic detection of a y-linked gene in xx males and xx true hermaphrodites. N Engl J Med. 1976 Sep 30; 295(14):750-4.
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    361. Bellin SS, Locke BZ, New M. The neighborhood health center as a mental health diagnostic service. Public Health Rep. 1976 Sep-Oct; 91(5):446-51.
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    362. Korth-Schutz S, Levine LS, New MI. Evidence for the adrenal source of androgens in precocious adrenarche. Acta Endocrinol (Copenh). 1976 Jun; 82(2):342-52.
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    363. Korth-Schutz S, Levine LS, New MI. Dehydroepiandrosterone sulfate (DS) levels, a rapid test for abnormal adrenal androgen secretion. J Clin Endocrinol Metab. 1976 Jun; 42(6):1005-13.
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    364. New MI, Baum CJ, Levine LS. Nomograms relating aldosterone excretion to urinary sodium and potassium in the pediatric population: their application to the study of childhood hypertension. Am J Cardiol. 1976 Mar 31; 37(4):658-66.
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    365. Saenger P, Levine LS, Wiedemann E, Schwartz E, New MI. Letter: Somatomedin in cerebral gigantism. J Pediatr. 1976 Jan; 88(1):155-6.
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    366. Saenger P, Rifkind AB, New MI. Changes in drug metabolism in children with thyroid disorders. J Clin Endocrinol Metab. 1976 Jan; 42(1):155-9.
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    367. New MI. Prenatal diagnosis of congenital adrenal hyperplasia. Prog Clin Biol Res. 1976; 10:205-19.
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    368. Doberne Y, New MI. Urinary androstanediol and testosterone in adults. J Clin Endocrinol Metab. 1976 Jan; 42(1):152-4.
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    369. Levine LS, Lewy JE, New MI. Hypertension in high school students. Evaluation in New York City. N Y State J Med. 1976 Jan; 76(1):40-4.
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    370. Saenger P, Schwartz E, Wiedemann E, Levine LS, Tsai M, New MI. The interaction of growth hormone, somatomedin and oestrogen in patients with Turner's syndrome. Acta Endocrinol (Copenh). 1976 Jan; 81(1):9-18.
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    371. Korth-Schutz S, Levine LS, New MI. Serum androgens in normal prepubertal and pubertal children and in children with precocious adrenarche. J Clin Endocrinol Metab. 1976 Jan; 42(1):117-24.
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    372. Doberne Y, Levine LS, New MI. Elevated urinary testosterone and androstanediol in precocious adrenarche. Pediatr Res. 1975 Oct; 9(10):794-7.
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    373. Rifkind AB, Bennett S, Forster ES, New MI. Components of the heme biosynthetic pathway and mixed function oxidase activity in human fetal tissues. Biochem Pharmacol. 1975 Apr 15; 24(8):839-46.
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    374. Lewy JE, New MI. Growth in children with renal failure. Am J Med. 1975 Jan; 58(1):65-8.
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    375. Simpson JL, Landey S, New M, German J. A previously unrecognized X-linked syndrome of dysmorphia. Birth Defects Orig Artic Ser. 1975; 11(2):18-24.
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    376. Parks GA, Korth-Schütz S, Penny R, Hilding RF, Dumars KW, Frasier SD, New MI. Variation in pituitary-gonadal function in adolescent male homosexuals and heterosexuals. J Clin Endocrinol Metab. 1974 Oct; 39(4):796-801.
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    377. Saenger P, Levine LS, Wiedemann E, Schwartz E, New MI. Letter: Growth with absent growth hormone by radioimmunoassay. J Pediatr. 1974 Jul; 85(1):137-8.
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    378. Bennett SP, Levine LS, Siegal EJ, Lewy JE, Susin M, Peterson RE, New MI. Juvenile hypertension caused by overproduction of renin within a renal segment. J Pediatr. 1974 May; 84(5):689-95.
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    379. Korth-Schutz S, Levine LS, Merkatz IR, New MI. An unusual case of Cushing's syndrome, hilus cell tumor and polycystic ovaries. J Clin Endocrinol Metab. 1974 May; 38(5):794-800.
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    380. Saenger P, Wiedemann E, Schwartz E, Korth-Schutz S, Lewy JE, Riggio RR, Rubin AL, Stenzel KH, New MI. Somatomedin and growth after renal transplantation. Pediatr Res. 1974 Mar; 8(3):163-9.
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    381. Parks GA, Dumars KW, Limbeck GA, Quinlivan WL, New MI. "True agonadism": a misnomer? J Pediatr. 1974 Mar; 84(3):375-80.
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    382. Canale VC, Steinherz P, New M, Erlandson M. Endocrine function in thalassemia major. Ann N Y Acad Sci. 1974; 232(0):333-45.
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    383. Saenger P, Shanies DD, New MI. Influence of medroxypregesteroneacetate on testosterone metabolism by cultured human fibroblasts: a model for drug-steroid interaction. J Clin Endocrinol Metab. 1973 Nov; 37(5):760-4.
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    384. Levine LS, Sonenberg M, New MI. Metabolic effects in children of a 37 amino acid fragment of bovine growth hormone. J Clin Endocrinol Metab. 1973 Oct; 37(4):607-15.
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    385. New MI, Siegal EJ, Peterson RE. Dexamethasone-suppressible hyperaldosteronism. J Clin Endocrinol Metab. 1973 Jul; 37(1):93-100.
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    386. Dahms WT, Gray G, Vrana M, New MI. Adrenocortical adenoma and ganglioneuroblastoma in a child. A case presenting as Cushing syndrome with virilization. Am J Dis Child. 1973 Apr; 125(4):608-11.
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    387. New MI, Levine LS. Congenital adrenal hyperplasia. Adv Hum Genet. 1973; 4:251-326.
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    388. Shanie DD, Hirschhorn K, New MI. Metabolism of testosterone- 14 C by cultured human cells. J Clin Invest. 1972 Jun; 51(6):1459-68.
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    389. Levine LS, New MI, Pitt P, Peterson RE. Androgen production in boys with sexual precocity and congenital adrenal hyperplasia. Metabolism. 1972 May; 21(5):457-64.
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    390. New MI, Schwartz E, Parks GA, Landey S, Wiedemann E. Pseudohypopituitary dwarfism with normal plasma growth hormone and low serum sulfation factor. J Pediatr. 1972 Apr; 80(4):620-6.
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    391. Opitz JM, Simpson JL, Sarto GE, Summitt RL, New M, German J. Pseudovaginal perineoscrotal hypospadias. Clin Genet. 1972; 3(1):1-26.
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    392. Zachmann M, Völlmin JA, New MI, Curtius HC, Prader A. Congenital adrenal hyperplasia due to deficiency of 11 -hydroxylation of 17 -hydroxylated steroids. J Clin Endocrinol Metab. 1971 Sep; 33(3):501-8.
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    393. Giombetti R, Hagstrom JW, Landey S, Young MC, New MI. Cushing's syndrome in infancy. A case complicated by monilial endocarditis. Am J Dis Child. 1971 Sep; 122(3):264-6.
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    394. Morillo-Cucci G, New M, Simpson JL, Allen FH, German J. Abnormalities of human sex chromosomes. 3. Duplication in the long arm of the Y chromosome (45,X-46,XYg+) in Y-gonadal dysgenesis. Ann Genet. 1971 Jun; 14(2):113-20.
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    395. Simpson JL, New M, Peterson RE, German J. Pseudovaginal perineoscrotal hypospadias (PPSH) in sibs. Birth Defects Orig Artic Ser. 1971 May; 7(6):140-4.
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    396. Levine LS, New MI. Preoperative detection of hidden testes. Am J Dis Child. 1971 Feb; 121(2):176-8.
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    397. Bullock LP, New MI. Testosterone and cortisol concentration in spermatic, adrenal and systemic venous blood in adult male guinea pigs. Endocrinology. 1971 Feb; 88(2):523-6.
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    398. New MI. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency. J Clin Invest. 1970 Oct; 49(10):1930-41.
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    399. New MI, Seaman MP. Secretion rates of cortisol and aldosterone precursors in various forms of congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1970 Mar; 30(3):361-71.
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    400. New MI. Antenatal diagnosis of the adrenogenital syndrome. Lancet. 1970 Jan 10; 1(7637):83.
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    401. Merkatz IR, New MI, Peterson RE, Seaman MP. Prenatal diagnosis of adrenogenital syndrome by amniocentesis. J Pediatr. 1969 Dec; 75(6):977-82.
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    402. Simpson JL, Allen FH, New M, German J. Absence of close linkage between the locus for Xg and the locus for anhidrotic ectodermal dysplasia. Vox Sang. 1969 Nov; 17(5):465-7.
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    403. New MI, Seaman MP, Peterson RE. A method for the simultaneous determination of the secretion rates of cortisol, 11-desoxycortisol, corticosterone, 11-desoxycorticosterone and aldosterone. J Clin Endocrinol Metab. 1969 Apr; 29(4):514-22.
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    404. New MI, Gross JM, Peterson RE. Double isotope dilution derivative technique for testosterone glucuronoside in urine. Acta Endocrinol (Copenh). 1968 May; 58(1):77-97.
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    405. New MI. Congenital adrenal hyperplasia. Pediatr Clin North Am. 1968 May; 15(2):395-407.
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    406. New MI, Peterson RE. Aldosterone in childhood. Adv Pediatr. 1968; 15:111-36.
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    407. Curi JF, Vanucci RC, Grossman H, New M. Elevated serum gonadotrophins in Silver's syndrome. Am J Dis Child. 1967 Dec; 114(6):658-61.
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    408. Nadler AC, Sonenberg M, New MI, Free CA. Growth hormone activity in man with components of tryptic digests of bovine growth hormone. Metabolism. 1967 Sep; 16(9):830-45.
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    409. Grossman H, New M. Precocious sexual development; roentgenographic aspects. Am J Roentgenol Radium Ther Nucl Med. 1967 May; 100(1):48-62.
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    410. New MI, Peterson RE. A new form of congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1967 Feb; 27(2):300-5.
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    411. Bongiovanni AM, Eberlein WR, Goldman AS, New M. Disorders of adrenal steroid biogenesis. Recent Prog Horm Res. 1967; 23:375-449.
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    412. Greenberg AJ, Arboit JM, New MI, Worthen HG. Normotensive secondary hyperaldosteronism. J Pediatr. 1966 Nov; 69(5):719-27.
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    413. New MI, Miller B, Peterson RE. Aldosterone excretion in normal children and in children with adrenal hyperplasia. J Clin Invest. 1966 Mar; 45(3):412-28.
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    414. New MI, Peterson RE. Disorders of aldosterone secretion in childhood. Pediatr Clin North Am. 1966 Feb; 13(1):43-58.
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    415. Potter RG, Wyon JB, New M, Gordon JE. Fetal wastage in eleven Punjab villages. Hum Biol. 1965 Sep; 37(3):262-73.
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    416. BAUER CH, NEW MI, MILLER JM. CEREBROSPINAL FLUID PROTEIN VALUES OF PREMATURE INFANTS. J Pediatr. 1965 Jun; 66:1017-22.
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    417. NEW MI. ENDOCRINE FACTORS IN GROWTH. Med Sci. 1964 Jun; 15:52-5.
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    418. NEW MI, ROBERTS TN, BIERMAN EL, READER GG. The significance of blood lipid alterations in diabetes mellitus. Diabetes. 1963 May-Jun; 12:208-12.
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    419. NEW M, MCNAMARA H, KRETCHMER N. Accumulation of para-aminohippurate by slices of kidney from rabbits of various ages. Proc Soc Exp Biol Med. 1959 Oct-Dec; 102:558-60.
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