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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.
Molecular Genetics & Genomic Medicine|January 10, 2019
Bilateral striatal necrosis due to homoplasmic mitochondrial 3697G>A mutation presents with incomplete penetrance and sex biasShanshan Zhong, Shumeng Wen, Yusen Qiu, et al.
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