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Journal Abstract Search

164 related items for PubMed ID: 3029158

  • 1. 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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  • 2. 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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  • 3. 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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  • 4. Isolated precocious pubarche: an approach.
    Balducci R, Boscherini B, Mangiantini A, Morellini M, Toscano V.
    J Clin Endocrinol Metab; 1994 Aug; 79(2):582-9. PubMed ID: 8045980
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  • 5. 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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  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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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  • 8. Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women.
    Pang SY, Lerner AJ, Stoner E, Levine LS, Oberfield SE, Engel I, New MI.
    J Clin Endocrinol Metab; 1985 Mar; 60(3):428-39. PubMed ID: 2982896
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  • 11. 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
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  • 13. Is heterozygosity for the steroid 21-hydroxylase deficiency responsible for hirsutism, premature pubarche, early puberty, and precocious puberty in children?
    Knorr D, Bidlingmaier F, Höller W, Kuhnle U, Meiler B, Nachmann A.
    Acta Endocrinol Suppl (Copenh); 1986 Jun; 279():284-9. PubMed ID: 3022523
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  • 14. Adrenal steroidogenic defects in children with precocious pubarche.
    del Balzo P, Borrelli P, Cambiaso P, Danielli E, Cappa M.
    Horm Res; 1992 Jun; 37(4-5):180-4. PubMed ID: 1337057
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  • 15. Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche.
    Ghizzoni L, Cappa M, Vottero A, Ubertini G, Carta D, Di Iorgi N, Gasco V, Marchesi M, Raggi V, Ibba A, Napoli F, Massimi A, Maghnie M, Loche S, Porzio O.
    Eur J Endocrinol; 2011 Aug; 165(2):307-14. PubMed ID: 21646284
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  • 16. Usefulness of an ACTH test in the diagnosis of nonclassical 21-hydroxylase deficiency among children presenting with premature pubarche.
    Ibáñez L, Bonnin MR, Zampolli M, Prat N, Alia PJ, Navarro MA.
    Horm Res; 1995 Aug; 44(2):51-6. PubMed ID: 7590632
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  • 17. 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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  • 18. Ovarian steroidogenic responses to gonadotropin-releasing hormone agonist testing with nafarelin in hirsute women with adrenal responses to adrenocorticotropin suggestive of 3 beta-hydroxy-delta 5-steroid dehydrogenase deficiency.
    Barnes RB, Ehrmann DA, Brigell DF, Rosenfield RL.
    J Clin Endocrinol Metab; 1993 Feb; 76(2):450-5. PubMed ID: 8381802
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  • 20. 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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