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Journal Abstract Search

141 related items for PubMed ID: 3484712

  • 1. 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; 23(2):74-7. PubMed ID: 3484712
    [Abstract] [Full Text] [Related]

  • 2. Detection of heterozygous carriers for 21-hydroxylase deficiency by plasma 21-deoxycortisol measurement.
    Gourmelen M, Gueux B, Pham Huu Trung MT, Fiet J, Raux-Demay MC, Girard F.
    Acta Endocrinol (Copenh); 1987 Dec; 116(4):507-12. PubMed ID: 2827419
    [Abstract] [Full Text] [Related]

  • 3. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype.
    Libber SM, Migeon CJ, Bias WB.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):727-30. PubMed ID: 3871788
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
    Colle M, Battin J.
    Arch Fr Pediatr; 1984 Jan; 41(7):483-5. PubMed ID: 6333857
    [Abstract] [Full Text] [Related]

  • 6. [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 Jan; 106(11-12):466-70. PubMed ID: 6335215
    [No Abstract] [Full Text] [Related]

  • 7. 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 Jan; 200():243-55. PubMed ID: 3001775
    [No Abstract] [Full Text] [Related]

  • 8. 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 Jan; 14(2):73-8. PubMed ID: 6268517
    [No Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. Morning salivary 17-hydroxyprogesterone is a useful screening test for nonclassical 21-hydroxylase deficiency.
    Zerah M, Pang SY, New MI.
    J Clin Endocrinol Metab; 1987 Aug 20; 65(2):227-32. PubMed ID: 3496350
    [Abstract] [Full Text] [Related]

  • 11. Serum 17-hydroxypregnenolone and 17-hydroxypregnenolone sulfate concentrations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Shimozawa K, Saisho S, Yata J, Kambegawa A.
    Endocrinol Jpn; 1988 Feb 20; 35(1):11-8. PubMed ID: 3260857
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Age of appearance of circadian rhythm in blood 17-hydroxyprogesterone in 21-hydroxylase deficiency.
    Sólyom J.
    Acta Physiol Hung; 1991 Apr 20; 78(2):107-10. PubMed ID: 1808976
    [Abstract] [Full Text] [Related]

  • 14. Prevalence of adrenal 21-hydroxylase deficiency in neonates born in the West Midlands: a retrospective study.
    Rudd BT.
    J Inherit Metab Dis; 1986 Apr 20; 9 Suppl 1():155-6. PubMed ID: 3097416
    [No Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. [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
    [Abstract] [Full Text] [Related]

  • 17. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review of current knowledge.
    Bacon GE, Kelch RP.
    J Endocrinol Invest; 1979 Jun 20; 2(1):93-100. PubMed ID: 385704
    [No Abstract] [Full Text] [Related]

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  • 20. Different gene defects in the salt-wasting (SW), simple virilizing (SV), and nonclassical (NC) types of congenital adrenal hyperplasia (CAH).
    Knorr D, Albert ED, Bidlingmaier F, Höller W, Scholz S.
    Ann N Y Acad Sci; 1985 Jun 20; 458():71-5. PubMed ID: 3879133
    [Abstract] [Full Text] [Related]

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