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Institution

Madeleine D. Harbison

TitleASSISTANT PROFESSOR
InstitutionMount Sinai
DepartmentEndocrinology - Adrenal Steroid Disorders
Address5 East 98th Street, 10flr.
New York NY 10029
Phone212-241-8210

     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. Appleby BS, Lu M, Bizzi A, Phillips MD, Berri SM, Harbison MD, Schonberger LB. Iatrogenic Creutzfeldt-Jakob disease from commercial cadaveric human growth hormone. Emerg Infect Dis. 2013 Apr; 19(4):682-4.
      View in: PubMed
    2. 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.
      View in: PubMed
    3. Harbison MD, Lin-Su K, New MI. Growth hormone treatment in children with congenital adrenal hyperplasia. Adv Exp Med Biol. 2011; 707:107.
      View in: PubMed
    4. Sharma J, Friedman D, Dave-Sharma S, Harbison M. Aortic distensibility and dilation in Turner's syndrome. Cardiol Young. 2009 Dec; 19(6):568-72.
      View in: PubMed
    5. 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.
      View in: PubMed
    6. Wajnrajch MP, Gertner JM, Sokoloff AS, Ten I, Harbison MD, Netchine I, Maheshwari HG, Goldstein DB, Amselem S, Baumann G, Leibel RL. Haplotype analysis of the growth hormone releasing hormone receptor locus in three apparently unrelated kindreds from the indian subcontinent with the identical mutation in the GHRH receptor. Am J Med Genet A. 2003 Jul 1; 120A(1):77-83.
      View in: PubMed
    7. Bongers EM, Opitz JM, Fryer A, Sarda P, Hennekam RC, Hall BD, Superneau DW, Harbison M, Poss A, van Bokhoven H, Hamel BC, Knoers NV. Meier-Gorlin syndrome: report of eight additional cases and review. Am J Med Genet. 2001 Aug 1; 102(2):115-24.
      View in: PubMed
    8. 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.
      View in: PubMed
    9. Thearle M, Horlick M, Bilezikian JP, Levy J, Gertner JM, Levine LS, Harbison M, Berdon W, Oberfield SE. Osteoporosis: an unusual presentation of childhood Crohn's disease. J Clin Endocrinol Metab. 2000 Jun; 85(6):2122-6.
      View in: PubMed
    10. 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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    11. Ostad M, Mininberg DT, Harbison M, Magid MS. Thoracolumbar accessory penis: etiology, diagnosis, and management. Urology. 1999 Feb; 53(2):425-7.
      View in: PubMed
    12. 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.
      View in: PubMed
    13. Donovan WD, Brill PW, Winchester P, Giampietro PF, Davis JG, Harbison M. Congenital fusion of the fourth and fifth metacarpals associated with primary gonadal failure. Skeletal Radiol. 1996 Apr; 25(3):269-71.
      View in: PubMed
    14. Wajnrajch MP, Gertner JM, Harbison MD, Chua SC, Leibel RL. Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse. Nat Genet. 1996 Jan; 12(1):88-90.
      View in: PubMed
    15. Wilson RC, Harbison MD, Krozowski ZS, Funder JW, Shackleton CH, Hanauske-Abel HM, Wei JQ, Hertecant J, Moran A, Neiberger RE, et al. Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess. J Clin Endocrinol Metab. 1995 Nov; 80(11):3145-50.
      View in: PubMed
    16. 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.
      View in: PubMed
    17. Cunningham-Rundles S, Harbison M, Guirguis S, Valacer D, Chretien PB. New perspectives on use of thymic factors in immune deficiency. Ann N Y Acad Sci. 1994 Aug 15; 730:71-83.
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    18. Zoppi S, Wilson CM, Harbison MD, Griffin JE, Wilson JD, McPhaul MJ, Marcelli M. Complete testicular feminization caused by an amino-terminal truncation of the androgen receptor with downstream initiation. J Clin Invest. 1993 Mar; 91(3):1105-12.
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    19. 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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    20. Harrison HH, Miller KL, Harbison MD, Slonim AE. Multiple serum protein abnormalities in carbohydrate-deficient glycoprotein syndrome: pathognomonic finding of two-dimensional electrophoresis? Clin Chem. 1992 Jul; 38(7):1390-2.
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    21. 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.
      View in: PubMed
    22. Harbison MD, Gertner JM. Permissive action of growth hormone on the renal response to dietary phosphorus deprivation. J Clin Endocrinol Metab. 1990 Apr; 70(4):1035-40.
      View in: PubMed
    23. Harbison M, Hassold T, Kobryn C, Jacobs PA. Molecular studies of the parental origin and nature of human X isochromosomes. Cytogenet Cell Genet. 1988; 47(4):217-22.
      View in: PubMed
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    Mount Sinai Profiles is managed by Conduits - The Institutes for Translational Sciences at Icahn School of Medicine, supported by the National Center for Research Resources and the National Center for Advancing Translational Sciences of the National Institutes of Health through Grant Number UL1TR000067