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Chuanzhu Yan

Showing results (1-10 of 211) with videos related to

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Journal of Neuroimmunology|October 12, 2016
Response to comments in The Journal of Neuroimmunology (December 16th, 2015)Ling Li, Tingjun Dai, Chuanzhu Yan
Neuromuscular Disorders : NMD|May 24, 2025
New insight in lipid storage myopathyBing Wen, Jingwen Xu, Chuanzhu Yan
JAMA Neurology|April 24, 2023
Ultrasonography of Muscle Vibration Caused by MYBPC1 VariantYing Zhao, Chuanzhu Yan, Kunqian Ji
Neurology India|March 9, 2016
Expanding the clinical spectrum of myopathy, encephalopathy, lactic acidosis, and stroke-like (MELAS) episode: A case with A3243G mitochondrial DNA mutation presenting as MELAS and congenital melanocytic naevi overlapFuchen Liu, Dong Zhang, Chuanzhu Yan
Journal of Human Genetics|January 25, 2018
Identification of IFRD1 variant in a Han Chinese family with autosomal dominant hereditary spastic paraplegia associated with peripheral neuropathy and ataxiaPengfei Lin, Dong Zhang, Guangrun Xu, et al.
Neurology|October 11, 2022
Author Response: Teaching NeuroImage: Leber Hereditary Optic Neuropathy With Longitudinal Spinal Cord Lesion Mimicking Spinal Cord InfarctionBing Zhao, Yuan Sun, Yongqing Zhang, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2022
Fluctuating ataxia caused by mitochondrial tRNA (Lys) gene m.8363G > A variantYing Zhao, Bing Zhao, Kunqian Ji, et al.
Stroke|February 16, 2024
Unraveling the Diagnostic Puzzle: Minor Stroke-Like Lesions and Normal Muscle Histopathology in MELAS SyndromeYing Zhao, Zhihong Xu, Chuanzhu Yan, et al.
Practical Neurology|February 7, 2024
Seven-and-a-half syndromeZhihong Xu, Yuying Zhao, Chuanzhu Yan, et al.
Metabolic Brain Disease|December 17, 2013
MERRF/MELAS overlap syndrome due to the m.3291T>C mutationKaiming Liu, Hui Zhao, Kunqian Ji, et al.
Pageof 22

Showing results (1-10 of 211) with videos related to

Sort By:
Pageof 22
Journal of Neuroimmunology|October 12, 2016
Response to comments in The Journal of Neuroimmunology (December 16th, 2015)Ling Li, Tingjun Dai, Chuanzhu Yan
Neuromuscular Disorders : NMD|May 24, 2025
New insight in lipid storage myopathyBing Wen, Jingwen Xu, Chuanzhu Yan
JAMA Neurology|April 24, 2023
Ultrasonography of Muscle Vibration Caused by MYBPC1 VariantYing Zhao, Chuanzhu Yan, Kunqian Ji
Neurology India|March 9, 2016
Expanding the clinical spectrum of myopathy, encephalopathy, lactic acidosis, and stroke-like (MELAS) episode: A case with A3243G mitochondrial DNA mutation presenting as MELAS and congenital melanocytic naevi overlapFuchen Liu, Dong Zhang, Chuanzhu Yan
Journal of Human Genetics|January 25, 2018
Identification of IFRD1 variant in a Han Chinese family with autosomal dominant hereditary spastic paraplegia associated with peripheral neuropathy and ataxiaPengfei Lin, Dong Zhang, Guangrun Xu, et al.
Neurology|October 11, 2022
Author Response: Teaching NeuroImage: Leber Hereditary Optic Neuropathy With Longitudinal Spinal Cord Lesion Mimicking Spinal Cord InfarctionBing Zhao, Yuan Sun, Yongqing Zhang, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2022
Fluctuating ataxia caused by mitochondrial tRNA (Lys) gene m.8363G > A variantYing Zhao, Bing Zhao, Kunqian Ji, et al.
Stroke|February 16, 2024
Unraveling the Diagnostic Puzzle: Minor Stroke-Like Lesions and Normal Muscle Histopathology in MELAS SyndromeYing Zhao, Zhihong Xu, Chuanzhu Yan, et al.
Practical Neurology|February 7, 2024
Seven-and-a-half syndromeZhihong Xu, Yuying Zhao, Chuanzhu Yan, et al.
Metabolic Brain Disease|December 17, 2013
MERRF/MELAS overlap syndrome due to the m.3291T>C mutationKaiming Liu, Hui Zhao, Kunqian Ji, et al.
Pageof 22