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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.
Journal of Neurology, Neurosurgery, and Psychiatry|October 12, 2010
NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASILZhaoxia Wang, Yun Yuan, Wei Zhang, et al.
Prion|June 3, 2025
Prion 2024 conference: from two decades of growth to a new journey forwardYifei Kong, Pengcheng Huang, Qi Shi, et al.
Brain and Behavior|January 3, 2022
Diverse myopathological features in the congenital myasthenia syndrome with GFPT1 mutationKaiyan Jiang, Yilei Zheng, Jing Lin, 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.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|September 27, 2023
Dyslipidemia is associated with progressive infarction in anterior circulation single subcortical infarction patientsShumeng Li, Liangbin Dong, Qin Huang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|March 28, 2026
Clinical characteristics and peripheral immune profile analysis of thymoma-associated myasthenia gravis with anti-titin antibodies: a multicenter, retrospective studyYeting Luo, Yusen Qiu, Jingyan Chai, et al.
Neuro-Degenerative Diseases|July 3, 2018
Novel ABCD1 Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus CallosumYusen Qiu, Ling Xin, Yuyao Wang, et al.
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