Increased urinary excretion of total 16α-hydroxypregnenolone in newborn infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Author:

Homoki Janos,Teller Walter M.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Genetics (clinical),Drug Discovery,Molecular Medicine

Reference15 articles.

1. Baillie TA, Brooks CJW, Chambaz EM, Glass RC, Madani C (1974) Comparison of isopentyloxime and benzoxyme trimethylsilyl ethers in the characterization of urinary steroids of newborn infants. In: Frigerio A, Castagnoli N (eds) Mass spectrometry in biochemistry and medicine. Raven, New York, pp 335–348

2. Bongiovanni AM, Kellenbenz G (1962) The adrenogenital syndrome with deficiency of 3β-hydroxysteroid dehydrogenase. J Clin Invest 41:2086–2092

3. Bradlow HL (1968) Extraction of steroid conjugates with a neutral resin. Steroids 11:265–272

4. Clayton BE (1970) Diagnosis and management of congenital adrenal hyperplasia. Proc Roy Soc Med 63:1042–1044

5. Desgres J, Bègue RJ, Curie G, Nivelon JL, Padieu P (1974) Identification and quantitative assay of steroids in congenital corticoadrenal hyperplasia in newborn infants by gas-liquid chromatography and gas chromatography-mass spectrometry. In: Frigerio A, Castagnoli N (eds) Mass spectrometry in biochemistry and medicine. Raven, New York, pp 349–359

Cited by 2 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. Biochemical aspects of congenital adrenal hyperplasia;Journal of Inherited Metabolic Disease;1986-03

2. Biochemical Aspects of Congenital Adrenal Hyperplasia;Practical Developments in Inherited Metabolic Disease: DNA Analysis, Phenylketonuria and Screening for Congenital Adrenal Hyperplasia;1986

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