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Neurology|November 24, 2025
Clinical Reasoning: A 16-Year-Old Adolescent Boy With Ophthalmoplegia and Unilateral PtosisYuxuan Lu, Haowei Wang, Zhaoxia Wang, et al.
Frontiers in Neurology|January 2, 2023
Unraveling rare form of adult-onset NIID by characteristic brain MRI features: A single-center retrospective reviewFan Li, Qi Wang, Ying Zhu, et al.
Neurobiology of Disease|December 25, 2023
Pathologic changes in neuronal intranuclear inclusion disease are linked to aberrant FUS interaction under hyperosmotic stressHui Wang, Yilei Zheng, Jiaxi Yu, et al.
Annals of Clinical and Translational Neurology|February 12, 2021
Mitochondrial morphology and MAVS-IFN1 signaling pathway in muscles of anti-MDA5 dermatomyositisYanyan Jiang, Yilin Liu, Yawen Zhao, et al.
Frontiers in Genetics|September 5, 2022
Juvenile-onset <i>PSAT1</i>-related neuropathy: A milder phenotype of serine deficiency disorderYu Shen, Yun Peng, Pengcheng Huang, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|January 13, 2026
Complement C5 Inhibitor Ameliorates a Case of DysferlinopathyShuaikun Kang, Qingqing Wang, He Lv, et al.
Rheumatology (Oxford, England)|August 7, 2024
Circulating cell-free DNA promotes inflammation in dermatomyositis patients with anti-NXP2 antibodies  via the cGAS/STING pathwayYikang Wang, Yawen Zhao, Qiang Gang, et al.
Frontiers in Aging Neuroscience|September 29, 2022
Urine cytological study in patients with clinicopathologically confirmed neuronal intranuclear inclusion diseaseYiyi Zhou, Pengcheng Huang, Zhaojun Huang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 14, 2026
CGG Repeat Expansion in GIPC1 is Associated with Childhood-Onset Hereditary AtaxiaYing Wu, Taoyun Ji, Quanzhen Tan, et al.
Journal of Neuropathology and Experimental Neurology|February 9, 2022
Widespread Mislocalization of FUS Is Associated With Mitochondrial Abnormalities in Skeletal Muscle in Amyotrophic Lateral Sclerosis With FUS MutationsMeng Yu, Xutong Zhao, Wei Wu, et al.
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