Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patients
Author:
Publisher
China Science Publishing & Media Ltd.
Subject
General Medicine
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. Epidemiology and distribution of 207 rare diseases in China: A systematic literature review;Intractable & Rare Diseases Research;2024-05-31
2. Metabolomic insights into maternal and neonatal complications in pregnancies affected by type 1 diabetes;Diabetologia;2023-08-24
3. Increased acylcarnitine ratio indices in newborn screening for carnitine-acylcarnitine translocase deficiency shows increased sensitivity and reduced false-positivity;Translational Pediatrics;2023-05
4. Case report: A novel c.1842_1845dup mutation of ETFDH in two Chinese siblings with multiple acyl-CoA dehydrogenase deficiency;Frontiers in Pediatrics;2023-01-04
5. Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Leading to Severe Metabolic Acidosis in a Young Adult;AACE Clinical Case Reports;2023-01
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