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137 related items for PubMed ID: 7626445

  • 21. Mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene in a patient with classic salt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia.
    Chang YT, Kappy MS, Iwamoto K, Wang J, Yang X, Pang S.
    Pediatr Res; 1993 Nov; 34(5):698-700. PubMed ID: 8284113
    [Abstract] [Full Text] [Related]

  • 22. Ontogeny and subcellular localization of 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) in the human and rat adrenal, ovary and testis.
    Pelletier G, Dupont E, Simard J, Luu-The V, Bélanger A, Labrie F.
    J Steroid Biochem Mol Biol; 1992 Oct; 43(5):451-67. PubMed ID: 1390295
    [Abstract] [Full Text] [Related]

  • 23. Congenital adrenal hyperplasia owing to 3 beta-hydroxysteroid dehydrogenase deficiency.
    Pang S.
    Endocrinol Metab Clin North Am; 2001 Mar; 30(1):81-99, vi-vii. PubMed ID: 11344940
    [Abstract] [Full Text] [Related]

  • 24. Congenital adrenal hyperplasia caused by a novel homozygous frameshift mutation 273 delta AA in type II 3 beta-hydroxysteroid dehydrogenase gene (HSD3B2) in three male patients of Afghan/Pakistani origin.
    Simard J, Rhéaume E, Leblanc JF, Wallis SC, Joplin GF, Gilbey S, Allanson J, Mettler G, Bettendorf M, Heinrich U.
    Hum Mol Genet; 1994 Feb; 3(2):327-30. PubMed ID: 8004103
    [Abstract] [Full Text] [Related]

  • 25. 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.
    Zerah M, Rhéaume E, Mani P, Schram P, Simard J, Labrie F, New MI.
    J Clin Endocrinol Metab; 1994 Dec; 79(6):1811-7. PubMed ID: 7989489
    [Abstract] [Full Text] [Related]

  • 26. Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa function.
    Pang S, Levine LS, Stoner E, Opitz JM, Pollack MS, Dupont B, New MI.
    J Clin Endocrinol Metab; 1983 Apr; 56(4):808-18. PubMed ID: 6300166
    [Abstract] [Full Text] [Related]

  • 27. A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: evaluation of gonadal function after puberty.
    Alos N, Moisan AM, Ward L, Desrochers M, Legault L, Leboeuf G, Van Vliet G, Simard J.
    J Clin Endocrinol Metab; 2000 May; 85(5):1968-74. PubMed ID: 10843183
    [Abstract] [Full Text] [Related]

  • 28. Male pseudohermaphroditism caused by nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) deficiency.
    Heinrich UE, Bettendorf M, Vecsei P.
    J Steroid Biochem Mol Biol; 1993 Apr; 45(1-3):83-5. PubMed ID: 8481355
    [Abstract] [Full Text] [Related]

  • 29. Structure and tissue-specific expression of 3 beta-hydroxysteroid dehydrogenase/5-ene-4-ene isomerase genes in human and rat classical and peripheral steroidogenic tissues.
    Labrie F, Simard J, Luu-The V, Pelletier G, Bélanger A, Lachance Y, Zhao HF, Labrie C, Breton N, de Launoit Y.
    J Steroid Biochem Mol Biol; 1992 Mar; 41(3-8):421-35. PubMed ID: 1562516
    [Abstract] [Full Text] [Related]

  • 30. The murine 3 beta-hydroxysteroid dehydrogenase multigene family: structure, function and tissue-specific expression.
    Payne AH, Clarke TR, Bain PA.
    J Steroid Biochem Mol Biol; 1995 Jun; 53(1-6):111-8. PubMed ID: 7626443
    [Abstract] [Full Text] [Related]

  • 31. Structure of the human type II 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4 isomerase (3 beta-HSD) gene: adrenal and gonadal specificity.
    Lachance Y, Luu-The V, Verreault H, Dumont M, Rhéaume E, Leblanc G, Labrie F.
    DNA Cell Biol; 1991 Dec; 10(10):701-11. PubMed ID: 1741954
    [Abstract] [Full Text] [Related]

  • 32. Absence of molecular defect in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3 beta-HSD activity.
    Chang YT, Zhang L, Alkaddour HS, Mason JI, Lin K, Yang X, Garibaldi LR, Bourdony CJ, Dolan LM, Donaldson DL.
    Pediatr Res; 1995 Jun; 37(6):820-4. PubMed ID: 7651769
    [Abstract] [Full Text] [Related]

  • 33. Molecular biology of the 3beta-hydroxysteroid dehydrogenase/delta5-delta4 isomerase gene family.
    Simard J, Ricketts ML, Gingras S, Soucy P, Feltus FA, Melner MH.
    Endocr Rev; 2005 Jun; 26(4):525-82. PubMed ID: 15632317
    [Abstract] [Full Text] [Related]

  • 34. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 Jun; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 35. Delayed diagnosis of congenital adrenal hyperplasia with salt wasting due to type II 3beta-hydroxysteroid dehydrogenase deficiency.
    Johannsen TH, Mallet D, Dige-Petersen H, Müller J, Main KM, Morel Y, Forest MG.
    J Clin Endocrinol Metab; 2005 Apr; 90(4):2076-80. PubMed ID: 15671104
    [Abstract] [Full Text] [Related]

  • 36. Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency.
    Lutfallah C, Wang W, Mason JI, Chang YT, Haider A, Rich B, Castro-Magana M, Copeland KC, David R, Pang S.
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2611-22. PubMed ID: 12050224
    [Abstract] [Full Text] [Related]

  • 37. The molecular and clinical spectrum of 3beta-hydroxysteroid dehydrogenase deficiency disorder.
    Pang S.
    Trends Endocrinol Metab; 1998 Feb; 9(2):82-6. PubMed ID: 18406247
    [Abstract] [Full Text] [Related]

  • 38. Studies of 3 beta-hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropin-stimulated delta 5-steroid levels.
    Sakkal-Alkaddour H, Zhang L, Yang X, Chang YT, Kappy M, Slover RS, Jorgensen V, Pang S.
    J Clin Endocrinol Metab; 1996 Nov; 81(11):3961-5. PubMed ID: 8923844
    [Abstract] [Full Text] [Related]

  • 39. Structure and expression of a new complementary DNA encoding the almost exclusive 3 beta-hydroxysteroid dehydrogenase/delta 5-delta 4-isomerase in human adrenals and gonads.
    Rhéaume E, Lachance Y, Zhao HF, Breton N, Dumont M, de Launoit Y, Trudel C, Luu-The V, Simard J, Labrie F.
    Mol Endocrinol; 1991 Aug; 5(8):1147-57. PubMed ID: 1944309
    [Abstract] [Full Text] [Related]

  • 40. Serum and urinary steroids in girls with precocious pubarche and/or hirsutism due to mild 3-beta-hydroxysteroid dehydrogenase deficiency.
    Sólyom J, Halász Z, Hosszú E, Gláz E, Vihko R, Orava M, Homoki J, Wudy SA, Teller WM.
    Horm Res; 1995 Aug; 44(3):133-41. PubMed ID: 7590644
    [Abstract] [Full Text] [Related]

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