21-Deoxycortisol is a Key Screening Marker for 21-Hydroxylase Deficiency
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference32 articles.
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2. Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia;Parsa;J Steroid Biochem Mol Biol,2017
3. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline;Speiser;J Clin Endocrinol Metab,2018
4. Update on diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Curr Opin Endocrinol Diabetes Obes,2018
5. Newborn screening for congenital adrenal hyperplasia with special reference to screening in Alaska;Pang;Ann N Y Acad Sci,1985
Cited by 6 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. Congenital Adrenal Hyperplasia;Pediatrics in Review;2024-02-01
2. Best Practice for Identification of Classical 21-Hydroxylase Deficiency Should Include 21 Deoxycortisol Analysis with Appropriate Isomeric Steroid Separation;International Journal of Neonatal Screening;2023-10-16
3. The use of liquid chromatography-tandem mass spectrometry in newborn screening for congenital adrenal hyperplasia: improvements and future perspectives;Frontiers in Endocrinology;2023-10-02
4. International Newborn Screening Practices for the Early Detection of Congenital Adrenal Hyperplasia;Hormone Research in Paediatrics;2023-05-15
5. Multiple 17-OHP Cutoff Co-Variates Fail to Improve 21-Hydroxylase Deficiency Screening Accuracy;International Journal of Neonatal Screening;2022-10-25
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