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-Reference-Cited by-同舟云学术

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

Published:2010-01 Issue:1 Volume:75 Page:34-52
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Christakoudi Sofia,Cowan David A.,Taylor Norman F.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference48 articles.

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4. Congenital adrenal hyperplasia caused by defect in steroid 21-hydroxylase. Establishment of definitive urinary steroid excretion pattern during first weeks of life;Shackleton;Clin Chim Acta,1976

5. The ontogeny of human drug-metabolizing enzymes: phase II conjugation enzymes and regulatory mechanisms;McCarver;J Pharmacol Exp Ther,2002

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