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Journal Abstract Search

126 related items for PubMed ID: 2962669

  • 1. 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; 14(11):633-7. PubMed ID: 2962669
    [Abstract] [Full Text] [Related]

  • 2. Urinary steroid excretion in 17 alpha-hydroxylase deficiency.
    Honour JW, Tourniaire J, Biglieri EG, Shackleton CH.
    J Steroid Biochem; 1978 Jun; 9(6):495-505. PubMed ID: 308577
    [No Abstract] [Full Text] [Related]

  • 3. 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; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 4. Metabolism of radiolabeled corticosterone in an adult with the 17 alpha-hydroxylase deficiency syndrome.
    Shackleton CH, Biglieri EG, Roitman E, Honour JW.
    J Clin Endocrinol Metab; 1979 Jun; 48(6):976-82. PubMed ID: 312808
    [Abstract] [Full Text] [Related]

  • 5. 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; 52(5):1039-42. PubMed ID: 6262355
    [Abstract] [Full Text] [Related]

  • 6. 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 May; 16(3-4):179-88. PubMed ID: 6982583
    [Abstract] [Full Text] [Related]

  • 7. Steroid excretion in a case of 17 alpha-hydroxylase deficiency investigated by computerized gas chromatography-mass spectrometry.
    Lisboa BP, Halket JM, Ganschow I, Ruiz-Gonzalez Mdel C.
    Acta Med Port; 1980 May; 1(4):433-49. PubMed ID: 7415860
    [No Abstract] [Full Text] [Related]

  • 8. Identification of 17-hydroxyprogesterone and other steroid hormones in saliva from a normal child and patients with congenital adrenal hyperplasia by plasmaspray liquid chromatography/mass spectrometry.
    Shindo N, Yamauchi N, Murayama K, Fairbrother A, Korlik S.
    Biomed Chromatogr; 1990 Jul; 4(4):171-4. PubMed ID: 2207381
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. Steroids excreted in urine by neonates with 21-hydroxylase deficiency: characterization, using GC-MS and GC-MS/MS, of the D-ring and side chain structure of pregnanes and pregnenes.
    Christakoudi S, Cowan DA, Taylor NF.
    Steroids; 2010 Jan 03; 75(1):34-52. PubMed ID: 19799922
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Determination of steroid profiles in healthy and diseased states: identification and quantitation of a block of 17 alpha-hydroxylase.
    Fennessey PV, Marsh PG, Orr ER, Burnstein P, Betz G.
    Clin Chim Acta; 1983 Mar 28; 129(1):3-11. PubMed ID: 6303630
    [Abstract] [Full Text] [Related]

  • 13. Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 2. Characterization, using GC-MS and GC-MS/MS, of pregnanes and pregnenes with an oxo- group on the A- or B-ring.
    Christakoudi S, Cowan DA, Taylor NF.
    Steroids; 2012 Apr 28; 77(5):382-93. PubMed ID: 22210448
    [Abstract] [Full Text] [Related]

  • 14. Seasonal changes in the production of two novel and abundant ovarian steroids in the channel catfish (Ictalurus punctatus).
    Ponthier JL, Shackleton CH, Trant JM.
    Gen Comp Endocrinol; 1998 Aug 28; 111(2):141-55. PubMed ID: 9679086
    [Abstract] [Full Text] [Related]

  • 15. A paradox: elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiency.
    Shackleton CH, Homoki J, Taylor NF.
    Steroids; 1987 Aug 28; 49(4-5):295-311. PubMed ID: 3502660
    [Abstract] [Full Text] [Related]

  • 16. 17 alpha-hydroxylase deficiency in genetic females. A report of two cases.
    Nagamani M, Dinh TV.
    J Reprod Med; 1986 Aug 28; 31(8):734-8. PubMed ID: 3490570
    [Abstract] [Full Text] [Related]

  • 17. Diagnosis of homozygosity and heterozygosity in congenital adrenal hyperplasia (CAH) and control of treatment.
    Knorr D, Bidlingmaier F, Höller W, Kuhnle U.
    J Steroid Biochem; 1983 Jul 28; 19(1B):645-53. PubMed ID: 6887889
    [Abstract] [Full Text] [Related]

  • 18. Congenital adrenal hyperplasia caused by defect in steroid 21-hydroxylase. Establishment of definitive urinary steroid excretion pattern during first weeks of life.
    Shackleton CH.
    Clin Chim Acta; 1976 Mar 15; 67(3):287-98. PubMed ID: 1261045
    [Abstract] [Full Text] [Related]

  • 19. The corticosteroid metabolic profile of the mouse.
    Shackleton CH, Hughes BA, Lavery GG, Walker EA, Stewart PM.
    Steroids; 2008 Oct 15; 73(11):1066-76. PubMed ID: 18502460
    [Abstract] [Full Text] [Related]

  • 20. Evidence against significant 19-nor-deoxycorticosterone production in patients with 17 alpha-hydroxylase deficiency.
    Shackleton CH.
    Clin Exp Hypertens A; 1982 Oct 15; 4(9-10):1529-39. PubMed ID: 6982794
    [Abstract] [Full Text] [Related]

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