128 related items for PubMed ID: 3265870
1. 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; 24(5):280-5. PubMed ID: 3265870
[Abstract] [Full Text] [Related]
2. [Reevaluation of recalled infants by neonatal mass screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Diagnostic value of pregnanetriolone in a single urine specimen using glass capillary gas chromatography].
Hikita Y.
Nihon Naibunpi Gakkai Zasshi; 1985 Mar 20; 61(3):197-219. PubMed ID: 3874793
[Abstract] [Full Text] [Related]
3. 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]
4. 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 20; 14(9):901-12. PubMed ID: 6975400
[No Abstract] [Full Text] [Related]
5. 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]
6. 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 23; 156():10-6. PubMed ID: 26493852
[Abstract] [Full Text] [Related]
7. 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 23; 58(4):741-7. PubMed ID: 22273564
[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. 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 Mar 15; 16(3-4):179-88. PubMed ID: 6982583
[Abstract] [Full Text] [Related]
10. Increased urinary excretion of total 16 alpha-hydroxypregnenolone in newborn infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Homoki J, Teller WM.
Klin Wochenschr; 1982 Apr 15; 60(8):407-10. PubMed ID: 6980322
[Abstract] [Full Text] [Related]
11. Difficulties in the diagnosis of congenital adrenal hyperplasia in early infancy: the 11 beta-hydroxylase defect.
Honour JW, Anderson JM, Shackleton CH.
Acta Endocrinol (Copenh); 1983 May 15; 103(1):101-9. PubMed ID: 6602444
[Abstract] [Full Text] [Related]
12. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
Hurwitz A, Brautbar C, Milwidsky A, Vecsei P, Milewicz A, Navot D, Rösler A.
J Clin Endocrinol Metab; 1985 Apr 15; 60(4):631-8. PubMed ID: 2982904
[Abstract] [Full Text] [Related]
13. 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 15; 14(11):633-7. PubMed ID: 2962669
[Abstract] [Full Text] [Related]
14. The diagnosis of congenital adrenal hyperplasia in the newborn by gas chromatography/mass spectrometry analysis of random urine specimens.
Caulfield MP, Lynn T, Gottschalk ME, Jones KL, Taylor NF, Malunowicz EM, Shackleton CH, Reitz RE, Fisher DA.
J Clin Endocrinol Metab; 2002 Aug 15; 87(8):3682-90. PubMed ID: 12161496
[Abstract] [Full Text] [Related]
15. [Determination of urinary 17 alpha-hydroxyprogesterone excretion using ELISA--evaluation of normal subjects and patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
Shibata Y.
Nihon Naibunpi Gakkai Zasshi; 1991 Aug 20; 67(8):819-39. PubMed ID: 1813324
[Abstract] [Full Text] [Related]
16. 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 Aug 20; 16(1-2):57-75. PubMed ID: 6278806
[No Abstract] [Full Text] [Related]
17. 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 Aug 20; 48(3-4):239-50. PubMed ID: 3502202
[Abstract] [Full Text] [Related]
18. Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms.
Kamrath C, Hartmann MF, Boettcher C, Wudy SA.
J Pediatr; 2014 Aug 20; 165(2):280-4. PubMed ID: 24862381
[Abstract] [Full Text] [Related]
19. 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 20; 151(1):24-8. PubMed ID: 1728539
[Abstract] [Full Text] [Related]
20. Biochemical aspects of congenital adrenal hyperplasia.
Honour J.
J Inherit Metab Dis; 1986 Jan 20; 9 Suppl 1():124-34. PubMed ID: 3097411
[Abstract] [Full Text] [Related]
Page: [Next] [New Search]
