These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (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; 120(3):341-53. PubMed ID: 6978779
    [TBL] [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; 147(3):257-62. PubMed ID: 3260557
    [TBL] [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; 48(3-4):239-50. PubMed ID: 3502202
    [TBL] [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; 24(5):280-5. PubMed ID: 3265870
    [TBL] [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; 22(3):363-9. PubMed ID: 3990286
    [TBL] [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; 45(5):421-34. PubMed ID: 8499349
    [TBL] [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; 16(3-4):179-88. PubMed ID: 6982583
    [TBL] [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; 67(3):287-98. PubMed ID: 1261045
    [TBL] [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; 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; 75(1):34-52. PubMed ID: 19799922
    [TBL] [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; 78(5):468-75. PubMed ID: 23454217
    [TBL] [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; 169(1):109-16. PubMed ID: 3479282
    [TBL] [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; 77(5):382-93. PubMed ID: 22210448
    [TBL] [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; 58(4):741-7. PubMed ID: 22273564
    [TBL] [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; 151(1):24-8. PubMed ID: 1728539
    [TBL] [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; 77(13):1487-501. PubMed ID: 22974828
    [TBL] [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; 156():10-6. PubMed ID: 26493852
    [TBL] [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; 56(2):222-9. PubMed ID: 6296182
    [TBL] [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; 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; 105(2):213-24. PubMed ID: 6931002
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.