Experiences during newborn screening for glutaric aciduria type 1: Diagnosis, treatment, genotype, phenotype, and outcomes-Reference-Cited by-同舟云学术

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Experiences during newborn screening for glutaric aciduria type 1: Diagnosis, treatment, genotype, phenotype, and outcomes

Published:2017-04 Issue:4 Volume:80 Page:253-261
ISSN:1726-4901
Container-title:Journal of the Chinese Medical Association
language:en
Short-container-title:

Author:

Tsai Fang-Chih,Lee Han-Jui,Wang An-Guor,Hsieh Shu-Chen,Lu Yung-Hsiu,Lee Ming-Che,Pai Ju-Shan,Chu Tzu-Hung,Yang Chia-Feng,Hsu Ting-Rong,Lai Chih-Jou,Tsai Ming-Tzu,Ho Ping-Hsun,Lin Min-Chieh,Cheng Ling-Yee,Chuang Ya-Chin,Niu Dau-Ming

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Cited by 27 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. Epidemiological burden of inborn errors of metabolism in low- and middle-income countries: a systematic review protocol;JBI Evidence Synthesis;2024-09-13

2. Prenatal Ultrasound and Magnetic Resonance Findings of Glutaric Acidemia Type 1 and Its Challenges in Prenatal Diagnosis;Journal of Medical Ultrasound;2024-07

3. Glutaric aciduria type 1 – the mask cerebral palsy (case report);Neuromuscular Diseases;2024-01-05

4. Update current understanding of neurometabolic disorders related to lysine metabolism;Epilepsy & Behavior;2023-09

5. Biochemical and molecular features of chinese patients with glutaric acidemia type 1 from Fujian Province, southeastern China;Orphanet Journal of Rare Diseases;2023-07-26

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