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Kon-Ping Lin

Showing results (21-30 of 80) with videos related to

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Annals of Clinical and Translational Neurology|May 29, 2020
Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variantYu-Shuen Tsai, Kon-Ping Lin, Kang-Yang Jih, et al.
Neurobiology of Aging|July 29, 2018
Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in TaiwanPei-Chien Tsai, Yi-Chu Liao, Kang-Yang Jih, et al.
Annals of Clinical and Translational Neurology|June 19, 2019
Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in TaiwanYun-Hsin Hsu, Kon-Ping Lin, Yuh-Cherng Guo, et al.
Neuromuscular Disorders : NMD|July 15, 2010
Clinical characterization and genetic analysis of a possible novel type of dominant Charcot-Marie-Tooth diseaseYi-Chung Lee, Tso-Ching Lee, Kon-Ping Lin, et al.
Clinical Neurology and Neurosurgery|March 9, 2004
Guillain-Barré syndrome coexisting with pericarditis or nephrotic syndrome after influenza vaccinationChuen-Der Kao, Jen-Tse Chen, Kon-Ping Lin, et al.
Neurobiology of Aging|May 18, 2010
FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALSChing-Paio Tsai, Bing-Wen Soong, Kon-Ping Lin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2011
Comparison of cerebellar ataxias: A three-year prospective longitudinal assessmentYi-chung Lee, Yi-chu Liao, Po-shan Wang, et al.
Journal of the Neurological Sciences|March 31, 2004
Myelin protein zero gene mutations in Taiwanese patients with Charcot-Marie-Tooth disease type 1Yi-Chung Lee, Bing-Wen Soong, Kon-Ping Lin, et al.
Journal of Neurology|February 25, 2005
Median nerve motor conduction velocity is concordant with myelin protein zero gene mutationYi-Chung Lee, Bing-Wen Soong, Yo-Tsen Liu, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 30, 2020
Investigating <i>TBP</i> CAG/CAA trinucleotide repeat expansions in a Taiwanese cohort with ALSKang-Yang Jih, Kon-Ping Lin, Pei-Chien Tsai, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Annals of Clinical and Translational Neurology|May 29, 2020
Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variantYu-Shuen Tsai, Kon-Ping Lin, Kang-Yang Jih, et al.
Neurobiology of Aging|July 29, 2018
Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in TaiwanPei-Chien Tsai, Yi-Chu Liao, Kang-Yang Jih, et al.
Annals of Clinical and Translational Neurology|June 19, 2019
Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in TaiwanYun-Hsin Hsu, Kon-Ping Lin, Yuh-Cherng Guo, et al.
Neuromuscular Disorders : NMD|July 15, 2010
Clinical characterization and genetic analysis of a possible novel type of dominant Charcot-Marie-Tooth diseaseYi-Chung Lee, Tso-Ching Lee, Kon-Ping Lin, et al.
Clinical Neurology and Neurosurgery|March 9, 2004
Guillain-Barré syndrome coexisting with pericarditis or nephrotic syndrome after influenza vaccinationChuen-Der Kao, Jen-Tse Chen, Kon-Ping Lin, et al.
Neurobiology of Aging|May 18, 2010
FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALSChing-Paio Tsai, Bing-Wen Soong, Kon-Ping Lin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2011
Comparison of cerebellar ataxias: A three-year prospective longitudinal assessmentYi-chung Lee, Yi-chu Liao, Po-shan Wang, et al.
Journal of the Neurological Sciences|March 31, 2004
Myelin protein zero gene mutations in Taiwanese patients with Charcot-Marie-Tooth disease type 1Yi-Chung Lee, Bing-Wen Soong, Kon-Ping Lin, et al.
Journal of Neurology|February 25, 2005
Median nerve motor conduction velocity is concordant with myelin protein zero gene mutationYi-Chung Lee, Bing-Wen Soong, Yo-Tsen Liu, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 30, 2020
Investigating <i>TBP</i> CAG/CAA trinucleotide repeat expansions in a Taiwanese cohort with ALSKang-Yang Jih, Kon-Ping Lin, Pei-Chien Tsai, et al.
Pageof 8