172 related items for PubMed ID: 6978779
1. 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]
2. 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 23; 147(3):257-62. PubMed ID: 3260557
[Abstract] [Full Text] [Related]
3. Late-onset 21-hydroxylase deficiency: reliable diagnosis by steroid analysis of random urine collections.
Shackleton CH, Irias J, McDonald C, Imperato-McGinley J.
Steroids; 1986 Apr 23; 48(3-4):239-50. PubMed ID: 3502202
[Abstract] [Full Text] [Related]
4. 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 23; 24(5):280-5. PubMed ID: 3265870
[Abstract] [Full Text] [Related]
5. 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 23; 22(3):363-9. PubMed ID: 3990286
[Abstract] [Full Text] [Related]
6. 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 23; 45(5):421-34. PubMed ID: 8499349
[Abstract] [Full Text] [Related]
7. 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 23; 16(3-4):179-88. PubMed ID: 6982583
[Abstract] [Full Text] [Related]
8. 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]
9. 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 15; 14(9):901-12. PubMed ID: 6975400
[No 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 15; 75(1):34-52. PubMed ID: 19799922
[Abstract] [Full Text] [Related]
11. 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 15; 78(5):468-75. PubMed ID: 23454217
[Abstract] [Full Text] [Related]
12. 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]
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 30; 77(5):382-93. PubMed ID: 22210448
[Abstract] [Full Text] [Related]
14. Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosterone.
Koyama Y, Homma K, Fukami M, Miwa M, Ikeda K, Ogata T, Hasegawa T, Murata M.
Clin Chem; 2012 Apr 30; 58(4):741-7. PubMed ID: 22273564
[Abstract] [Full Text] [Related]
15. Urinary excretion of 17-hydroxypregnanolones in patients with different forms of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
Homoki J, Sólyom J, Wachter U, Teller WM.
Eur J Pediatr; 1992 Jan 30; 151(1):24-8. PubMed ID: 1728539
[Abstract] [Full Text] [Related]
16. Steroids excreted in urine by neonates with 21-hydroxylase deficiency. 3. Characterization, using GC-MS and GC-MS/MS, of androstanes and androstenes.
Christakoudi S, Cowan DA, Taylor NF.
Steroids; 2012 Nov 30; 77(13):1487-501. PubMed ID: 22974828
[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. 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 30; 56(2):222-9. PubMed ID: 6296182
[Abstract] [Full Text] [Related]
19. Steroids in newborns and infants. The changing pattern of urinary steroid excretion during infancy.
Shackleton CH, Gustafsson JA, Mitchell FL.
Acta Endocrinol (Copenh); 1973 Sep 30; 74(1):157-67. PubMed ID: 4800836
[No Abstract] [Full Text] [Related]
20. 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]
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