Comparison of two different radioimmunoassays to measure 17-hydroxyprogesterone during treatment monitoring of children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference20 articles.
1. Congenital adrenal hyperplasia;Speiser;N Engl J Med,2003
2. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Endocr Rev,2000
3. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data;New;J Clin Endocrinol Metab,1983
4. Precocious pubarche: distinguishing late-onset congenital adrenal hyperplasia from premature adrenarche;Armengaud;J Clin Endocrinol Metab,2009
5. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany;Krone;J Clin Endocrinol Metab,2000
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. An electrochemical immunoassay based on trepang-like gold electrodes and nanogold functionalized flower-like hierarchical carbon materials with improved sensitivity;New Journal of Chemistry;2015
2. 17-Hydroxyprogesterone in children, adolescents and adults;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2014-04-07
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