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UnknownThe Value of Reducing Inconclusive and False-Positive Newborn Screening Results for Congenital Hypothyroidism, Congenital Adrenal Hyperplasia and Maple Syrup Urine Disease in The Netherlands.
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S-EPMC11503431 | biostudies-literature
UnknownTreatment of congenital adrenal hyperplasia in children aged 0-3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure.
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S-EPMC9066592 | biostudies-literature
UnknownReal-World Estimates of Adrenal Insufficiency-Related Adverse Events in Children With Congenital Adrenal Hyperplasia.
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S-EPMC7990061 | biostudies-literature
UnknownGenetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
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S-EPMC7278165 | biostudies-literature
UnknownOligogenic analysis across broad phenotypes of 46,XY differences in sex development associated with NR5A1/SF-1 variants: findings from the international SF1next study.
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S-EPMC11925193 | biostudies-literature
UnknownClinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development.
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S-EPMC10797150 | biostudies-literature
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