The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference17 articles.
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2. The early recognition of the 21-hydroxylase deficiency variety of congenital adrenal hyperplasia;Steen;Clin Chim Acta,1980
3. An all-glass solid sampling device for open tubular columns in gas chromatography;Van den Berg;Chromatografia,1972
4. Steroid in newborns and infants. Identification of steroids in urine from newborn infants;Shackleton;Steroids,1971
5. Polar corticosteroids in human neonatal urine synthesis and gaschromatography-mass-spectrometry of ring A reduced 6-hydroxylated corticosteroids;Derks;Steroids,1978
Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A proof of concept of a machine learning algorithm to predict late-onset 21-hydroxylase deficiency in children with premature pubic hair;The Journal of Steroid Biochemistry and Molecular Biology;2022-06
2. 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;Steroids;2013-05
3. 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;Steroids;2010-01
4. New identified 15β-hydroxylated 21-deoxy-pregnanes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency;The Journal of Steroid Biochemistry and Molecular Biology;1993-05
5. A neonate with idiopathic hyperaldosteronism;Pediatric Nephrology;1991-11
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