A neonate with idiopathic hyperaldosteronism-Reference-Cited by-同舟云学术

A neonate with idiopathic hyperaldosteronism

Published:1991-11 Issue:6 Volume:5 Page:680-684
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Veenhoven Reinier H.,Vande Walle Johan G.,Donckerwolcke Raymond A.,Wit Jan M.,Griffiven Arjan W.,Derkx Frans H.,Schalekamp Maarten A.

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF00857870.pdf

Reference26 articles.

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3. Ploeg KR van der Wolthers GB, Nagel GT, Volmer M, Drayer NM (1982) The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern. Clin Chim Acta 120: 341?353

4. Koopman BJ, Lokerse IJG, Verwey H, Nagel GT, Molen JC van der (1986) Improved gas chromatographic-mass fragmentographic assay for tetrahydroaldosterone and aldosterone in urine. J Chromatogr 378: 283?292

5. Boer P, Hene RJ, Koomans HA, Nieuwenhuis MG, Geyskes GG, Dorhout Mees EJ (1983) Blood and extracellular fluid volume in patients with Bartter's syndrome. Arch Intern Med 143: 1902?1905

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