Apparent double defect in C11β and C21-steroid hydroxylation in congenital adrenal hyperplasia
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry
Reference17 articles.
1. Biosynthesis of corticoids;Samuels,1975
2. Inborn errors of steroid biosynthesis;Finkelstein;Physiol. Rev.,1979
3. Congenital adrenal hyperplasia with hypertension: unusual steroid pattern in blood and urine;Eberlein;J. clin. Endocr. Metab.,1955
4. Plasma and urinary corticoids in the hypertensive form of congenital adrenal hyperplasia;Eberlein;J. biol. Chem.,1956
5. Pregnane-3α,17,20α-triol and pregnane-3α,17,20α-triol-11-one excretion by patients with adrenocortical dysfunction;Cox;J. clin. Invest.,1957
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1. Steroid Profiling by LC-MS/MS in Nonsecreting and Subclinical Cortisol-Secreting Adrenocortical Adenomas;The Journal of Clinical Endocrinology & Metabolism;2015-09
2. 21-Hydroxylase Deficiency Transiently Mimicking Combined 21- and 11β-Hydroxylase Deficiency;Journal of Pediatric Endocrinology and Metabolism;2008-01
3. Serum 21-Deoxycortisol, 17-Hydroxyprogesterone, and 11-Deoxycortisol in Classic Congenital Adrenal Hyperplasia: Clinical and Hormonal Correlations and Identification of Patients with 11β-Hydroxylase Deficiency among a Large Group with Alleged 21-Hydroxylase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2006-06
4. Late-onset congenital adrenal hyperplasia in women with hirsutism;European Journal of Clinical Investigation;1992-10
5. Secondary Biosynthetic Defects in Women with Late-Onset Congenital Adrenal Hyperplasia;New England Journal of Medicine;1990-09-27
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