Urinary GC–MS steroid metabotyping in treated children with congenital adrenal hyperplasia.
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference29 articles.
1. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline;Speiser;J. Clin. Endocrinol. Metab.,2018
2. The urinary steroidome of treated children with CAH;Kamrath;J. Steroid Biochem. Mol. Biol.,2017
3. Monitoring of therapy in congenital adrenal hyperplasia;Dauber;Clin. Chem.,2010
4. Height velocity defined metabolic control in children with congenital adrenal hyperplasia using urinary steroid GC-MS analysis;Kamrath;J. Clin. Endocrinol. Metab.,2019
5. Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?;Charmandari;J. Clin. Endocrinol. Metab.,2001
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