Mineralocorticoid Deficiency and Treatment in Congenital Adrenal Hyperplasia
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Springer Science and Business Media LLC
Reference28 articles.
1. Population-Wide Evaluation of Disease Manifestation in Relation to Molecular Genotype in Steroid 21-Hydroxylase (CYP21) Deficiency: Good Correlation in a Well Defined Population
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1. Blood Pressure in Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency;Hormone Research in Paediatrics;2023-08-23
2. High-dose fludrocortisone therapy was transiently required in a female neonate with 21-hydroxylase deficiency;CLIN PEDIATR ENDOCRI;2022
3. Nonsense variant of NR0B1 causes hormone disorders associated with congenital adrenal hyperplasia;Scientific Reports;2021-08-09
4. Bioelectrical Impedance Phase Angle and Its Determinants in Patients with Classic Congenital Adrenal Hyperplasia;Journal of the American College of Nutrition;2021-03-25
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