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Pediatric Investigation|April 6, 2022
Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow-upWeihua Zhang, Jiuwei Li, Xiuwei Zhuo, et al.
Frontiers in Neurology|September 19, 2022
Oculogyric crisis mimicked epilepsy in a Chinese aromatic L-amino acid decarboxylase-deficiency patient: A case reportHongmei Wang, Jiahong Li, Ji Zhou, et al.
Multiple Sclerosis and Related Disorders|September 12, 2022
Mycophenolate mofetil: An alternative disease-modifying agent for MOG-IgG-associated disorders in childhood: A single-center bidirectional cohort studyJi Zhou, Jiuwei Li, Changhong Ren, et al.
Epilepsia|December 22, 2025
The symmetrical claustrum sign in pediatric febrile infection-related epilepsy syndrome: Diagnostic value and clinical implicationsXiaodi Han, Changhong Ren, Hua Cheng, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|April 24, 2024
Clinical Presentation, Management, and Diagnostic Performance of 2021 Criteria for Paraneoplastic Neurologic Syndromes in ChildhoodJi Zhou, Mei Jin, Yan Su, et al.
Developmental Medicine and Child Neurology|September 15, 2022
Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese childrenJiaping Wang, Fang Fang, Changhong Ding, et al.
Frontiers in Immunology|August 28, 2020
Study of B Cell Repertoire in Patients With Anti-N-Methyl-D-Aspartate Receptor EncephalitisJingjing Feng, Siyuan Fan, Yinwei Sun, et al.
Journal of Neuromuscular Diseases|July 16, 2025
Pathogenic mechanisms and clinical insights into B3GALNT2-related alpha-dystroglycanopathiesXiaona Fu, Hui Wang, Wenjia Chai, et al.
Epilepsy & Behavior : E&B|July 14, 2022
Functional connectivity differences in speech production networks in Chinese children with Rolandic epilepsyYun Wu, Fang Fang, Ke Li, et al.
Pediatric Neurology|January 19, 2024
Encephalitis is an Important Phenotype of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Diseases: A Single-Center Cohort StudyChanghong Ren, Anna Zhou, Ji Zhou, et al.
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