Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF01954376.pdf
Reference13 articles.
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2. Globerman H, Rosler A, Theodor R, New MI, White PC (1988) An inherited defect in aldosterone biosynthesis caused by mutation in or near the gene for 11 hydroxylase. N Engl J Med 319:1193–1197
3. Healy JK, Elliot AJ (1977) The effect of a natriuretic dose of angiotensin or a rabbit kidney composition. Clin Sci 38:727–739
4. Kater CE, Biglieri EG, Rost CR, Schambelan M, Hirai J, Chang BCF, Brust N (1985) The constant plasma hydroxycorticosterone to aldosterone ratio: an expression of the efficacy of corticosterone methyl oxidase type II activity in disorders with variable aldosterone production. J Clin Endocrinol Metab 60:225–228
5. Kater CE, Biglieri EG, Brust N, Chang B, Hirai J, Irony I (1989) Stimulation and suppression of the mineralcorticoid hormones in normal subjects and adrenocortical disorders. Endocr Rev 10:149–164
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