Female Preponderance in Congenital Adrenal Hyperplasia due to CYP21 Deficiency in England: Implications for Neonatal Screening-Reference-Cited by-同舟云学术

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Female Preponderance in Congenital Adrenal Hyperplasia due to CYP21 Deficiency in England: Implications for Neonatal Screening

Published:2005 Issue:1 Volume:63 Page:22-28
ISSN:1663-2818
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Nordenström A.,Ahmed S.,Jones J.,Coleman M.,Price D.A.,Clayton P.E.,Hall C.M.

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Reference23 articles.

1. Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

2. Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation

3. Population-Wide Evaluation of Disease Manifestation in Relation to Molecular Genotype in Steroid 21-Hydroxylase (CYP21) Deficiency: Good Correlation in a Well Defined Population

Cited by 52 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. Cross-Cultural Disparities in Psychosocial Research with Individuals with Classical Congenital Adrenal Hyperplasia: A Scoping Review;Hormone Research in Paediatrics;2023-08-08

2. Assessment of the Degree of Clinical Suspicion of 21-Hydroxylase Deficiency Prior to the Newborn Screening Result;Hormone and Metabolic Research;2023-06-16

3. Epidemiology and diagnostic trends of congenital adrenal hyperplasia in Denmark: a retrospective, population-based study;The Lancet Regional Health - Europe;2023-05

4. Congenital adrenal hyperplasia;The Lancet;2023-01

5. Long-Term Outcomes of Congenital Adrenal Hyperplasia;Endocrinology and Metabolism;2022-08-31

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