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Journal Abstract Search

262 related items for PubMed ID: 6982583

  • 1. Steroid spectrum in human urine as revealed by gas chromatography V. Identification and quantitation of 3 alpha, 20 alpha-dihydroxy-5-beta pregnan-11-one (11-keto-pregnanediol) during different stages of development in children with C/21 hydroxylase deficiency.
    Kecskés L, Czira G.
    Acta Biochim Biophys Acad Sci Hung; 1981; 16(3-4):179-88. PubMed ID: 6982583
    [Abstract] [Full Text] [Related]

  • 2. Steroid spectrum in human urine as revealed by gas chromatography. IV. Changes in the exception of 16-oxygenated neutral steroids by children with 21-hydroxylase deficiency during different stages of development.
    Kecskés L, Juricskay Z, Kosztoláni G, Szécsényi M.
    Acta Biochim Biophys Acad Sci Hung; 1981; 16(1-2):57-75. PubMed ID: 6278806
    [No Abstract] [Full Text] [Related]

  • 3. Steroid spectrum in human urine as revealed by gas chromatography. III. Identification and quantitation of pregnenediol at different stages of bodily development.
    Kecskés L, Juricskay Z, Czira G.
    Acta Biochim Biophys Acad Sci Hung; 1980; 15(1):49-55. PubMed ID: 7457075
    [Abstract] [Full Text] [Related]

  • 4. Steroid spectrum in human urine as revealed by gas chromatography. VI. Pregnanediol excretion values and 3 beta-hydroxy-delta 5-steroid dehydrogenase activity of girls at different stage of development.
    Kecskés L, Juricskay Z, Szécsényi M, Palotás E.
    Acta Biochim Biophys Hung; 1986; 21(1-2):67-80. PubMed ID: 3466494
    [Abstract] [Full Text] [Related]

  • 5. Significance of 3alpha, 17 alpha-dihydroxy-5beta-pregnane-20-one in the diagnosis of congenital adrenal hyperplasia.
    Kecskés L, Tényi I, Németh M, Juricskay Z, Temesi M.
    Endokrinologie; 1975 Sep; 66(1):94-9. PubMed ID: 1225520
    [Abstract] [Full Text] [Related]

  • 6. The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern.
    van der Ploeg KR, Wolthers BG, Nagel GT, Volmer M, Drayer NM.
    Clin Chim Acta; 1982 Apr 23; 120(3):341-53. PubMed ID: 6978779
    [Abstract] [Full Text] [Related]

  • 7. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry.
    Burstein P, Marsh P, Fennessey P, Betz G.
    Obstet Gynecol; 1983 Mar 23; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 8. [Diagnosis of the adrenogenital syndrome caused by 11beta-hydroxylase deficiency using gas chromatographic-mass spectrometric analysis of the urinary steroid profile].
    Wudy SA, Homoki J, Wachter UA, Teller WM.
    Dtsch Med Wochenschr; 1997 Jan 03; 122(1-2):3-10; discussion 11. PubMed ID: 9064231
    [Abstract] [Full Text] [Related]

  • 9. Dynamics of adrenal steroidogenesis in childhood: changes in the excretion of 16-oxygenated- and 11-oxygenated-steroids by 21-hydroxylase deficient children at various ages.
    Kecskés L.
    Endokrinologie; 1982 Oct 03; 80(2):151-7. PubMed ID: 6297879
    [Abstract] [Full Text] [Related]

  • 10. Identification of new steroids in patients with 17 alpha-hydroxylase deficiency by capillary gas chromatography/mass spectrometry.
    Blau N, Zachmann M, Kempken B, Staudenmann W, Möhr E, Curtius HC.
    Biomed Environ Mass Spectrom; 1987 Nov 03; 14(11):633-7. PubMed ID: 2962669
    [Abstract] [Full Text] [Related]

  • 11. The evaluation of testicular endocrine function before and in puberty. Effect of a single dose of human chorionic gonadotropin on urinary steroid excretion under normal and pathological conditions.
    Zachmann M.
    Acta Endocrinol Suppl (Copenh); 1972 Nov 03; 164():3-94. PubMed ID: 4403436
    [No Abstract] [Full Text] [Related]

  • 12. Diagnosis of 21-hydroxylase deficiency in newborn infants by GC-MS of urinary steroids.
    Yong AB, Pitt JJ, Montalto J, Davies HE, Warne GL, Connelly JF.
    Aust Paediatr J; 1988 Oct 03; 24(5):280-5. PubMed ID: 3265870
    [Abstract] [Full Text] [Related]

  • 13. Capillary gas chromatography as a tool for characterization of urinary steroid excretion in patients with congenital adrenal hyperplasia.
    Vierhapper H, Nowotny P, Waldhäusl W, Frisch H.
    J Steroid Biochem; 1985 Mar 03; 22(3):363-9. PubMed ID: 3990286
    [Abstract] [Full Text] [Related]

  • 14. Identification of 15 beta-hydroxylated C21 steroids in the neo-natal period: the role of 3 alpha,15 beta,17 alpha-trihydroxy-5 beta-pregnan-20-one in the perinatal diagnosis of congenital adrenal hyperplasia (CAH) due to a 21-hydroxylase deficiency.
    Joannou GE.
    J Steroid Biochem; 1981 Sep 03; 14(9):901-12. PubMed ID: 6975400
    [No Abstract] [Full Text] [Related]

  • 15. Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients.
    Zachmann M, Tassinari D, Prader A.
    J Clin Endocrinol Metab; 1983 Feb 03; 56(2):222-9. PubMed ID: 6296182
    [Abstract] [Full Text] [Related]

  • 16. Urinary excretion of pregnanetriol and 5 -pregnenetriol in two forms of congenital adrenal hyperplasia.
    Bongiovanni AM, Eberlein WR, Moshang T.
    J Clin Invest; 1971 Dec 03; 50(12):2751-4. PubMed ID: 5129323
    [Abstract] [Full Text] [Related]

  • 17. [A contribution to the therapy of the congenital adrenal hyperplasia (author's transl)].
    Gleispach H.
    Wien Klin Wochenschr; 1974 Sep 20; 86(17):508-11. PubMed ID: 4408420
    [No Abstract] [Full Text] [Related]

  • 18. Detection of late onset steroid 21-hydroxylase deficiency by capillary gas chromatographic profiling of urinary steroids in children and adolescents.
    Homoki J, Solyom J, Teller WM.
    Eur J Pediatr; 1988 Apr 20; 147(3):257-62. PubMed ID: 3260557
    [Abstract] [Full Text] [Related]

  • 19. Fluorescence high performance liquid chromatographic determination of 3 alpha-hydroxysteroids in urine of 21-hydroxylase deficiency.
    Kawasaki T, Maeda M, Tsuji A.
    Biomed Chromatogr; 1986 Feb 20; 1(1):1-6. PubMed ID: 3506812
    [Abstract] [Full Text] [Related]

  • 20. Steroid excretion in urine during suppression and stimulation of adrenals in the 17 alpha-hydroxylase deficiency syndrome.
    Honour J, Millar G, Roitman E, Shackleton C.
    J Clin Endocrinol Metab; 1981 May 20; 52(5):1039-42. PubMed ID: 6262355
    [Abstract] [Full Text] [Related]

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