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Journal Abstract Search

131 related items for PubMed ID: 6931002

  • 1. The early recognition of the 21-hydroxylase deficiency variety of congenital adrenal hyperplasia.
    Steen G, Tas AC, Ten Noever De Brauw MC, Drayer NM, Wolthers BG.
    Clin Chim Acta; 1980 Aug 04; 105(2):213-24. PubMed ID: 6931002
    [Abstract] [Full Text] [Related]

  • 2. New identified 15 beta-hydroxylated 21-deoxy-pregnanes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Kraan GP, Wolthers BG, van der Molen JC, Nagel GT, Drayer NM, Joannou GE.
    J Steroid Biochem Mol Biol; 1993 May 04; 45(5):421-34. PubMed ID: 8499349
    [Abstract] [Full Text] [Related]

  • 3. Analysis of glucocorticoid metabolites in the neonatal period: catabolism of cortisone acetate by an infant with 21-hydroxylase deficiency.
    Taylor NF, Curnow DH, Shackleton CH.
    Clin Chim Acta; 1978 May 02; 85(3):219-29. PubMed ID: 306899
    [Abstract] [Full Text] [Related]

  • 4. The characterization of polar corticosteroids in the urine of the macaque monkey (macaca fascicularis) and the baboon (papio hamadryas).
    Setchell KD, Gontscharow NP, Axelson M, Sjövall J.
    Acta Endocrinol (Copenh); 1975 Jul 02; 79(3):535-50. PubMed ID: 1173507
    [Abstract] [Full Text] [Related]

  • 5. 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 02; 77(5):382-93. PubMed ID: 22210448
    [Abstract] [Full Text] [Related]

  • 6. The partial characterization of 1-oxygenated steroids from urine of a hypertensive newborn child.
    Edwards RW, Trafford DJ.
    Biochem J; 1968 Jun 02; 108(2):185-93. PubMed ID: 5665883
    [Abstract] [Full Text] [Related]

  • 7. Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 4. Characterization, using GC-MS and GC-MS/MS, of 11oxo-pregnanes and 11oxo-pregnenes.
    Christakoudi S, Cowan DA, Taylor NF.
    Steroids; 2013 May 02; 78(5):468-75. PubMed ID: 23454217
    [Abstract] [Full Text] [Related]

  • 8. The in vitro metabolism of 11β-hydroxyprogesterone and 11-ketoprogesterone to 11-ketodihydrotestosterone in the backdoor pathway.
    van Rooyen D, Gent R, Barnard L, Swart AC.
    J Steroid Biochem Mol Biol; 2018 Apr 02; 178():203-212. PubMed ID: 29277707
    [Abstract] [Full Text] [Related]

  • 9. Urinary excretion of 5beta-pregnane-3alpha,20alpha,21-triol in human gestation.
    Begue RJ, Moriniere M, Padieu P.
    Biomed Mass Spectrom; 1978 Mar 02; 5(3):184-7. PubMed ID: 630058
    [Abstract] [Full Text] [Related]

  • 10. 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 02; 14(9):901-12. PubMed ID: 6975400
    [No Abstract] [Full Text] [Related]

  • 11. Multicomponent gas chromatographic analysis of urinary steroids excreted by an infant with a defect in aldosterone biosynthesis.
    Shackleton CH, Honour JW, Dillon M, Milla P.
    Acta Endocrinol (Copenh); 1976 Apr 02; 81(4):762-73. PubMed ID: 946566
    [Abstract] [Full Text] [Related]

  • 12. Synthesis of 17,20alpha/beta-dihydroxy-4-pregnen-3-one and 5beta-pregnanes in spermatozoa of primary and 17alpha-methyltestosterone-induced secondary male grouper (Epinephelus coioides).
    Lee ST, Kime DE, Lam TJ, Tan CH.
    Gen Comp Endocrinol; 1998 Oct 02; 112(1):1-9. PubMed ID: 9748397
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. [Diagnosis of steroid-11-beta hydroxylase deficiency].
    Sólyom J, Cholnoky P, Helmuth D, Dietrich K, Nagy E, Varga I, Gláz E.
    Orv Hetil; 1986 Sep 07; 127(36):2171-5. PubMed ID: 3463925
    [No Abstract] [Full Text] [Related]

  • 15. 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 07; 75(1):34-52. PubMed ID: 19799922
    [Abstract] [Full Text] [Related]

  • 16. Detection of 3 beta-hydroxysteroid dehydrogenase deficiency in a newborn by means of urinary steroid analysis.
    Wolthers BG, de Vries IJ, Volmer M, Nagel GT.
    Clin Chim Acta; 1987 Oct 30; 169(1):109-16. PubMed ID: 3479282
    [Abstract] [Full Text] [Related]

  • 17. Diagnosis of 21-hydroxylase deficiency by urinary metabolite ratios using gas chromatography-mass spectrometry analysis: Reference values for neonates and infants.
    Kamrath C, Hartmann MF, Boettcher C, Zimmer KP, Wudy SA.
    J Steroid Biochem Mol Biol; 2016 Feb 30; 156():10-6. PubMed ID: 26493852
    [Abstract] [Full Text] [Related]

  • 18. A new marker for early diagnosis of 21-hydroxylase deficiency: 3beta,16alpha,17alpha-trihydroxy-5alpha-pregnane-7,20-dione.
    Christakoudi S, Cowan DA, Taylor NF.
    J Steroid Biochem Mol Biol; 2010 Aug 30; 121(3-5):574-81. PubMed ID: 20302934
    [Abstract] [Full Text] [Related]

  • 19. Use of a radioimmunoassay which detects C21 steroids with a 5beta-reduced, 3alpha-hydroxylated configuration to identify and measure steroids involved in final oocyte maturation in female plaice (Pleuronectes platessa).
    Inbaraj RM, Scott AP, Vermeirssen EL.
    Gen Comp Endocrinol; 1997 Jan 30; 105(1):50-61. PubMed ID: 9000467
    [Abstract] [Full Text] [Related]

  • 20. Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms.
    Kamrath C, Hartmann MF, Boettcher C, Wudy SA.
    J Pediatr; 2014 Aug 30; 165(2):280-4. PubMed ID: 24862381
    [Abstract] [Full Text] [Related]

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