CURRENT THERAPY THE MANAGEMENT OF CLASSICAL CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.1990.tb03893.x/fullpdf
Reference25 articles.
1. Monitoring treatment in congenital adrenal hyperplasia;Appan;Archives of Disease in Childhood,1989
2. Polycystic ovaries in childhood;Brook;British Medical Journal,1988
3. Experience with long term therapy in congenital adrenal hyperplasia;Brook;Journal of Pediatrics,1974
4. Prenatal treatment of Congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency;David;Journal of Pediatrics,1984
5. Aldosterone and Cortisol production rates in infants and children with CAH suggesting different 21-hydroxylation defects in salt losers and non-salt losers;Degenhart;Acta Endocrinologica,1965
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1. Development of the congenital adrenal hyperplasia knowledge assessment questionnaire (CAHKAQ);Journal of Clinical Nursing;2008-07
2. Development of Rapid and Sensitive One‐Step Direct Enzyme Linked Immunosorbent Assay for 17‐α‐OH‐Progesterone in Serum;Journal of Immunoassay and Immunochemistry;2008-03-18
3. Blood Pressure in Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency;Journal of Pediatric Endocrinology and Metabolism;2006-01
4. Different states of clinical control are associated with changes in IGF-I and IGFBPs in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Clinical Endocrinology;2004-07
5. Surface-activated chemical ionization ion trap mass spectrometry in the analysis of 21-deoxycortisol in blood;Rapid Communications in Mass Spectrometry;2004-05-27
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