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Clinical Genetics|September 1, 2025
Novel Biallelic Variants in DLD Gene Cause a Reversible Sensory NeuropathyLu Wang, Ying Xiong, Kaiyan Jiang, et al.
BMC Neurology|March 7, 2025
Imaging predictors of progressive infarction in patients with anterior circulation small subcortical infarctionLiangbin Dong, Xiaocheng Mao, Kaiyan Jiang, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 7, 2022
Pathological changes of the sural nerve in patients with familial episodic pain syndromeYilei Zheng, Pengcheng Huang, Shumeng Li, 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 PSAT1-related neuropathy: A milder phenotype of serine deficiency disorderYu Shen, Yun Peng, Pengcheng Huang, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 22, 2025
Clinical Phenotype Spectrum in Two Large Chinese Families With Rippling Muscle Disease Caused by CAV-3 c.80G>AYu Shen, Kaiyan Jiang, Hancun Yi, et al.
Cell Communication and Signaling : CCS|February 7, 2025
uN2CpolyG-mediated p65 nuclear sequestration suppresses the NF-κB-NLRP3 pathway in neuronal intranuclear inclusion diseaseYu Shen, Kaiyan Jiang, Dandan Tan, et al.
Annals of Clinical and Translational Neurology|January 13, 2026
Diffusion Spectrum Imaging Maps Early Axonal Loss and a Unique Progressive Signal in Neuronal Intranuclear Inclusion DiseaseKaiyan Jiang, Yixiu Pei, Xiaobao Hu, et al.
Channels (Austin, Tex.)|May 9, 2024
Clinical and genetic characteristics of myotonia congenita in Chinese populationYuting He, Yusen Qiu, Ying Xiong, et al.
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