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Journal Abstract Search

305 related items for PubMed ID: 8923844

  • 1. 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
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  • 2. 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
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  • 3. Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.
    Mermejo LM, Elias LL, Marui S, Moreira AC, Mendonca BB, de Castro M.
    J Clin Endocrinol Metab; 2005 Mar; 90(3):1287-93. PubMed ID: 15585552
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  • 5. Adrenal steroidogenic function in a black and Hispanic population with precocious pubarche.
    Oberfield SE, Mayes DM, Levine LS.
    J Clin Endocrinol Metab; 1990 Jan; 70(1):76-82. PubMed ID: 2152934
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  • 10. Genetic defects of steroidogenesis in premature pubarche.
    Temeck JW, Pang SY, Nelson C, New MI.
    J Clin Endocrinol Metab; 1987 Mar; 64(3):609-17. PubMed ID: 3029158
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  • 11. 3 alpha-Androstanediol glucuronide in premature and normal pubarche.
    Riddick LM, Garibaldi LR, Wang ME, Senne AR, Klimah PE, Clark AT, Levine LS, Oberfield SE, Pang SY.
    J Clin Endocrinol Metab; 1991 Jan; 72(1):46-50. PubMed ID: 1846006
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  • 12. Carriers for type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test.
    Pang S, Carbunaru G, Haider A, Copeland KC, Chang YT, Lutfallah C, Mason JI.
    Clin Endocrinol (Oxf); 2003 Mar; 58(3):323-31. PubMed ID: 12608938
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  • 14. Mild adrenal 3 beta-hydroxysteroid dehydrogenase deficiency in children with accelerated growth, premature pubarche and/or hirsutism.
    Nishi Y, Tezuka T.
    Eur J Pediatr; 1992 Jan; 151(1):19-23. PubMed ID: 1309452
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  • 16. Hypothalamic-pituitary-gonadal axis function in pubertal male and female siblings with glucocorticoid-treated nonsalt-wasting 3 beta-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia.
    Chang YT, Kulin HE, Garibaldi L, Suriano MJ, Bracki K, Pang S.
    J Clin Endocrinol Metab; 1993 Nov; 77(5):1251-7. PubMed ID: 8077318
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  • 17. Detection and functional characterization of the novel missense mutation Y254D in type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) gene of a female patient with nonsalt-losing 3 beta HSD deficiency.
    Sanchez R, Rhéaume E, Laflamme N, Rosenfield RL, Labrie F, Simard J.
    J Clin Endocrinol Metab; 1994 Mar; 78(3):561-7. PubMed ID: 8126127
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  • 18. Nonclassical 3 beta-hydroxysteroid dehydrogenase deficiency in young girls with hirsutism and premature pubarche.
    Nishi Y.
    Endocrinol Jpn; 1990 Oct; 37(5):763-7. PubMed ID: 2150813
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  • 19. Nonsalt-losing male pseudohermaphroditism due to the novel homozygous N100S mutation in the type II 3 beta-hydroxysteroid dehydrogenase gene.
    Mébarki F, Sanchez R, Rhéaume E, Laflamme N, Simard J, Forest MG, Bey-Omar F, David M, Labrie F, Morel Y.
    J Clin Endocrinol Metab; 1995 Jul; 80(7):2127-34. PubMed ID: 7608265
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  • 20. Molecular basis of congenital adrenal hyperplasia in two siblings with classical nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency.
    Rhéaume E, Sanchez R, Simard J, Chang YT, Wang J, Pang S, Labrie F.
    J Clin Endocrinol Metab; 1994 Oct; 79(4):1012-8. PubMed ID: 7962268
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