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Yo-Tsen Liu

Showing results (41-50 of 54) with videos related to

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Plos One|August 27, 2015
Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic ProfilesYi-Chu Liao, Cheng-Tsung Hsiao, Jong-Ling Fuh, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 2012
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testingSinead M Murphy, Matilde Laura, Katherine Fawcett, et al.
Neurology|August 8, 2014
A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG functionPei-Chien Tsai, Yen-Hua Huang, Yuh-Cherng Guo, et al.
Frontiers in Neurology|November 3, 2018
Aberrant Sensory Gating of the Primary Somatosensory Cortex Contributes to the Motor Circuit Dysfunction in Paroxysmal Kinesigenic DyskinesiaYo-Tsen Liu, Yi-Chieh Chen, Shang-Yeong Kwan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 15, 2017
Genetic and clinical characteristics of <i>NEFL</i>-related Charcot-Marie-Tooth diseaseAlejandro Horga, Matilde Laurà, Zane Jaunmuktane, et al.
Scientific Reports|December 26, 2019
Gamma Knife radiosurgery for cerebral cavernous malformationCheng-Chia Lee, Wei-Hsin Wang, Huai-Che Yang, et al.
Epilepsia|May 20, 2022
Clinical characteristics and long-term outcome of cerebral cavernous malformations-related epilepsyYen-Cheng Shih, Chien-Chen Chou, Syu-Jyun Peng, et al.
Brain : a Journal of Neurology|April 4, 2017
A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathyPei-Chien Tsai, Bing-Wen Soong, Inès Mademan, et al.
Nature Communications|March 10, 2026
Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical laminationHaw-Yuan Cheng, Chen Liu, Chiao-Wen Nien, et al.
Brain : a Journal of Neurology|February 14, 2015
Defects of mutant DNMT1 are linked to a spectrum of neurological disordersJonathan Baets, Xiaohui Duan, Yanhong Wu, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Plos One|August 27, 2015
Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic ProfilesYi-Chu Liao, Cheng-Tsung Hsiao, Jong-Ling Fuh, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 12, 2012
Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testingSinead M Murphy, Matilde Laura, Katherine Fawcett, et al.
Neurology|August 8, 2014
A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG functionPei-Chien Tsai, Yen-Hua Huang, Yuh-Cherng Guo, et al.
Frontiers in Neurology|November 3, 2018
Aberrant Sensory Gating of the Primary Somatosensory Cortex Contributes to the Motor Circuit Dysfunction in Paroxysmal Kinesigenic DyskinesiaYo-Tsen Liu, Yi-Chieh Chen, Shang-Yeong Kwan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 15, 2017
Genetic and clinical characteristics of <i>NEFL</i>-related Charcot-Marie-Tooth diseaseAlejandro Horga, Matilde Laurà, Zane Jaunmuktane, et al.
Scientific Reports|December 26, 2019
Gamma Knife radiosurgery for cerebral cavernous malformationCheng-Chia Lee, Wei-Hsin Wang, Huai-Che Yang, et al.
Epilepsia|May 20, 2022
Clinical characteristics and long-term outcome of cerebral cavernous malformations-related epilepsyYen-Cheng Shih, Chien-Chen Chou, Syu-Jyun Peng, et al.
Brain : a Journal of Neurology|April 4, 2017
A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathyPei-Chien Tsai, Bing-Wen Soong, Inès Mademan, et al.
Nature Communications|March 10, 2026
Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical laminationHaw-Yuan Cheng, Chen Liu, Chiao-Wen Nien, et al.
Brain : a Journal of Neurology|February 14, 2015
Defects of mutant DNMT1 are linked to a spectrum of neurological disordersJonathan Baets, Xiaohui Duan, Yanhong Wu, et al.
Pageof 6