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Journal Abstract Search

157 related items for PubMed ID: 6257014

  • 21. 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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  • 22. Ovarian steroidogenesis in an adrenalectomized girl with 21-hydroxylase deficiency.
    Zachmann M, Manella B, Kempken B, Knorr-Muerset G, Atares M, Prader A.
    Clin Endocrinol (Oxf); 1984 Nov; 21(5):575-82. PubMed ID: 6094047
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  • 24. Contribution of plasma androstenedione to 5 alpha-androstanediol glucuronide in women with idiopathic hirsutism.
    Gompel A, Wright F, Kuttenn F, Mauvais-Jarvis P.
    J Clin Endocrinol Metab; 1986 Feb; 62(2):441-4. PubMed ID: 3941165
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  • 25. Extraadrenal steroid 21-hydroxylase activity in a woman with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Winkel CA, Casey ML, Worley RJ, Madden JD, MacDonald PC.
    J Clin Endocrinol Metab; 1983 Jan; 56(1):104-7. PubMed ID: 6600168
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  • 28. Detection of the heterozygous state in siblings of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Gutai JP, Lee PA, Johnsonbaugh RE, Gareis F, Urban MD, Migeon CJ.
    J Pediatr; 1979 May; 94(5):770-2. PubMed ID: 221633
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  • 29. Serum 3 alpha-androstanediol glucuronide measurements in sexually mature women with congenital adrenal hyperplasia during therapy.
    Reiner BJ, Donohoue PA, Migeon CJ, Berkovitz GD.
    J Clin Endocrinol Metab; 1989 Jul; 69(1):105-9. PubMed ID: 2732292
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  • 30. Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing. A family study.
    Kauschansky A, Kaufman H, Zamir R, Elian E.
    Horm Res; 1981 Jul; 14(2):73-8. PubMed ID: 6268517
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  • 31. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
    Peterson RE, Imperato-McGinley J, Gautier T, Shackleton C.
    N Engl J Med; 1985 Nov 07; 313(19):1182-91. PubMed ID: 2932643
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  • 33. Multiple or single 21-hydroxylases in congenital adrenal hyperplasia?
    West CD, Atcheson JB, Stanchfield JB, Rallison ML, Chavré VJ, Tyler FH.
    J Steroid Biochem; 1979 Oct 07; 11(4):1413-9. PubMed ID: 316046
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  • 34. 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 Oct 07; 279():284-9. PubMed ID: 3022523
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  • 35. [Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].
    Liotta A, Cammarata M, Corsello G, Ferrara D, Giuffrè L.
    Pediatr Med Chir; 1987 Oct 07; 9(3):309-10. PubMed ID: 2823235
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  • 36. Clinically silent congenital adrenal hyperplasia masquerading as ectopic adrenocorticotropic hormone syndrome.
    Georgitis WJ.
    Am J Med; 1986 Apr 07; 80(4):703-8. PubMed ID: 3008554
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  • 37. A case of late-onset congenital adrenal hyperplasia due to partial 3 beta-hydroxysteroid dehydrogenase deficiency.
    Hattori N, Ishihara T, Moridera K, Hino M, Ikekubo K, Kurahachi H.
    Endocr J; 1993 Feb 07; 40(1):107-9. PubMed ID: 7951484
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  • 38. Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.
    Laron Z, Pollack MS, Zamir R, Roitman A, Dickerman Z, Levine LS, Lorenzen F, O'Neill GJ, Pang S, New MI, Dupont B.
    Hum Immunol; 1980 Jul 07; 1(1):55-66. PubMed ID: 6266983
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  • 39. ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism.
    Siegel SF, Finegold DN, Lanes R, Lee PA.
    N Engl J Med; 1990 Sep 27; 323(13):849-54. PubMed ID: 2168515
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  • 40. Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents.
    Emans SJ, Grace E, Fleischnick E, Mansfield MJ, Crigler JF.
    Pediatrics; 1983 Nov 27; 72(5):690-5. PubMed ID: 6314235
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