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Journal Abstract Search

114 related items for PubMed ID: 3097416

  • 1. Prevalence of adrenal 21-hydroxylase deficiency in neonates born in the West Midlands: a retrospective study.
    Rudd BT.
    J Inherit Metab Dis; 1986; 9 Suppl 1():155-6. PubMed ID: 3097416
    [No Abstract] [Full Text] [Related]

  • 2. [Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 1. Enzyme immunoassay of dried blood 17 alpha-hydroxyprogesterone and its application to neonatal screening for congenital adrenal hyperplasia].
    Fukushi M, Arai O, Mizushima Y, Takasugi N, Fujieda K, Matsuura N.
    Nihon Naibunpi Gakkai Zasshi; 1986 Jun 20; 62(6):683-96. PubMed ID: 3530828
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  • 3. [Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 3. An enzyme-linked immunosorbent assay for dried blood 17 alpha-hydroxyprogesterone].
    Fukushi M, Arai O, Mizushima Y, Takasugi N, Fujieda K, Matsuura N.
    Nihon Naibunpi Gakkai Zasshi; 1987 Feb 20; 63(2):113-22. PubMed ID: 3494638
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  • 7. Serum androgen concentrations in neonates and young infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Pang S, Levine LS, Chow DM, Faiman C, New MI.
    Clin Endocrinol (Oxf); 1979 Dec 20; 11(6):575-84. PubMed ID: 161209
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  • 9. Circadian variation of plasma 17-hydroxyprogesterone among heterozygotic carriers of 21-hydroxylase deficiency (salt-losing form).
    Urban MD, Migeon CJ, Lee PA.
    Horm Res; 1986 Dec 20; 23(2):74-7. PubMed ID: 3484712
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  • 10. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Pang SY, Wallace MA, Hofman L, Thuline HC, Dorche C, Lyon IC, Dobbins RH, Kling S, Fujieda K, Suwa S.
    Pediatrics; 1988 Jun 20; 81(6):866-74. PubMed ID: 3259306
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  • 11. Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency.
    David M, Forest MG.
    J Pediatr; 1984 Nov 20; 105(5):799-803. PubMed ID: 6334149
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  • 12. [Detection of heterozygotes in the classic type of congenital adrenal hyperplasia due to a 21-hydroxylase defect in our population as based on hormonal studies and HLA typing].
    Dumić M, Tajić M, Brkljacić L, Mardesić D, Radica A, Lukenda M, Gjurić G, Jovanović V, Plavsić V, Kastelan A.
    Lijec Vjesn; 1984 Nov 20; 106(11-12):466-70. PubMed ID: 6335215
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  • 13. The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).
    Carmina E, Gagliano AM, Rosato F, Maggiore M, Jannì A.
    J Endocrinol Invest; 1984 Apr 20; 7(2):89-92. PubMed ID: 6327799
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  • 14. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
    Colle M, Battin J.
    Arch Fr Pediatr; 1984 Apr 20; 41(7):483-5. PubMed ID: 6333857
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  • 15. Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Khandekar S, Lata V, Dash RJ.
    Indian J Med Res; 1990 Apr 20; 92():79-82. PubMed ID: 2164496
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  • 19. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients.
    Livieri C, Belvedere M, Martinetti M, Beluffi G, Fiori P, Cogliati CR, Goffredo V, Lorini R, Severi F.
    Prog Clin Biol Res; 1985 Apr 20; 200():243-55. PubMed ID: 3001775
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