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Journal of Human Genetics|September 3, 2024
Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286 T > C identified as a hotspot mutation in Chinese patients with a stable natural historyHuafang Jiang, Chaolong Xu, Ruoyu Duan, et al.
Mitochondrion|November 20, 2021
Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center studyYuqing Shi, Guohong Chen, Dan Sun, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|March 15, 2020
Long-term efficacy of mycophenolate mofetil in myelin oligodendrocyte glycoprotein antibody-associated disorders: A prospective studyShengde Li, Haitao Ren, Yan Xu, et al.
Gene|January 30, 2023
De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndromeXiaoting Lou, Yuwei Zhou, Zhimei Liu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 16, 2021
Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center studyWeihua Zhang, Changhong Ren, Xiaohui Wang, et al.
Frontiers in Pediatrics|July 16, 2021
Immunotherapies for Anti-N-M-methyl-D-aspartate Receptor Encephalitis: Multicenter Retrospective Pediatric Cohort Study in ChinaShiqi Guang, Jiannan Ma, Xiaotun Ren, et al.
Pediatric Investigation|June 20, 2025
Effectiveness and safety of perampanel for pediatric patients with epilepsy: A real-world study from ChinaXiaohui Wang, Taoyun Ji, Maomao Liu, et al.
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