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deficiency of steroid 21- hydroxylase
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OMIM - Congenital disorder
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The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with…
Diagnosis and management of classical congenital adrenal hyperplasia.
Impact of nasal continuous positive airway pressure for congenital adrenal hyperplasia with obstruct…
Overestimation of final height prediction in patients with classical congenital adrenal hyperplasia …
Bone mineral density, bone markers, and fractures in adult males with congenital adrenal hyperplasia…
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A Study Examining Doses of Abiraterone Acetate in Adult Women With 21-Hydroxylase Deficiency
Examining Genetic Differences Among People With 21-Hydroxylase Deficiency
Determining the Long-Term Effects of Prenatal Dexamethasone Treatment in Children With 21-Hydroxylas…
Screening and Stimulation Testing for Residual Secretion of Adrenal Steroid Hormones in Autoimmune A…
Safety and Efficacy Study of Phenoptin in Subjects With Hyperphenylalaninemia Due to BH4 Deficiency
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