Gabapentin for complex regional pain syndrome in Machado-Joseph disease: a case report

Por Lo, Yang-Ching, Liao, Kwong-Kum, Lee, Yi-Chung, Soong, Bing-Wen
Publicado em 2011

An Intronic CArG Box Regulates Cysteine-rich Protein 2 Expression in the Adult but not Developing Vasculature

Por Chen, Chung-Huang, Wu, Meng-Ling, Lee, Yi-Chung, Layne, Matthew D., Yet, Shaw-Fang
Publicado em 2010

Rapid progressive ALS in a patient with a DNAJC7 loss-of-function mutation

Por Jih, Kang-Yang, Tsai, Pei-Chien, Tsai, Yu-Shuen, Liao, Yi-Chu, Lee, Yi-Chung
Publicado no Neurol Genet (2020)

Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias

Por Hsiao, Cheng-Tsung, Liu, Yo-Tsen, Liao, Yi-Chu, Hsu, Ting-Yi, Lee, Yi-Chung, Soong, Bing-Wen
Publicado no PLoS One (2017)

Correction: Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias

Por Hsiao, Cheng-Tsung, Liu, Yo-Tsen, Liao, Yi-Chu, Hsu, Ting-Yi, Lee, Yi-Chung, Soong, Bing-Wen
Publicado no PLoS One (2018)

Mutation spectrum of Charcot‐Marie‐Tooth disease among the Han Chinese in Taiwan

Por Hsu, Yun‐Hsin, Lin, Kon‐Ping, Guo, Yuh‐Cherng, Tsai, Yu‐Shuen, Liao, Yi‐Chu, Lee, Yi‐Chung
Publicado no Ann Clin Transl Neurol (2019)

Hand‐onset weakness is a common feature of ALS patients with a NEK1 loss‐of‐function variant

Por Tsai, Yu‐Shuen, Lin, Kon‐Ping, Jih, Kang‐Yang, Tsai, Pei‐Chien, Liao, Yi‐Chu, Lee, Yi‐Chung
Publicado no Ann Clin Transl Neurol (2020)

Two Novel De Novo GARS Mutations Cause Early-Onset Axonal Charcot-Marie-Tooth Disease

Por Liao, Yi-Chu, Liu, Yo-Tsen, Tsai, Pei-Chien, Chang, Chia-Ching, Huang, Yen-Hua, Soong, Bing-Wen, Lee, Yi-Chung
Publicado no PLoS One (2015)

Spinocerebellar ataxia type 36 in the Han Chinese

Por Lee, Yi-Chung, Tsai, Pei-Chien, Guo, Yuh-Cherng, Hsiao, Cheng-Tsung, Liu, Guan-Ting, Liao, Yi-Chu, Soong, Bing-Wen
Publicado no Neurol Genet (2016)

Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy

Por Liao, Yi-Chu, Tsai, Pei-Chien, Lin, Thy-Sheng, Hsiao, Cheng-Tsung, Chao, Nai-Chen, Lin, Kon-Ping, Lee, Yi-Chung
Publicado no Sci Rep (2017)

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

Por Chao, Hua‐Chuan, Liao, Yi‐Chu, Liu, Yo‐Tsen, Guo, Yuh‐Cherng, Chang, Fu‐Pang, Lee, Yi‐Chung, Lin, Kon‐Ping
Publicado no Ann Clin Transl Neurol (2019)

Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

Por Chou, Cheng‐Ta, Soong, Bing‐Wen, Lin, Kon‐Ping, Tsai, Yu‐Shuen, Jih, Kang‐Yang, Liao, Yi‐Chu, Lee, Yi‐Chung
Publicado no Ann Clin Transl Neurol (2020)

Cerebral Microbleed Burdens in Specific Brain Regions Are Associated With Disease Severity of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalop...

Por Chung, Chih‐Ping, Chen, Jiun‐Wei, Chang, Feng‐Chi, Li, Wei‐Chi, Lee, Yi‐Chung, Chen, Li‐Fen, Liao, Yi‐Chu
Publicado no J Am Heart Assoc (2020)

The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2 among the Han Chinese in Taiwan

Por Lin, Kon-Ping, Soong, Bing-Wen, Yang, Chih-Chao, Huang, Li-Wen, Chang, Ming-Hong, Lee, I-Hui, Antonellis, Antony, Lee, Yi-Chung
Publicado em 2011

Correction: The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2 among the Han Chinese in Taiwan

Por Lin, Kon-Ping, Soong, Bing-Wen, Yang, Chih-Chao, Huang, Li-Wen, Chang, Ming-Hong, Lee, I-Hui, Antonellis, Anthony, Lee, Yi-Chung
Publicado em 2012

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia

Por Chen, Ying-Hao, Lee, Yi-Chung, Tsai, Yu-Shuen, Guo, Yuh-Cherng, Hsiao, Cheng-Tsung, Tsai, Pei-Chien, Huang, Jin-An, Liao, Yi-Chu, Soong, Bing-Wen
Publicado no PLoS One (2017)

Incidental findings on brain magnetic resonance imaging: systematic review and meta-analysis

Por Morris, Zoe, Whiteley, William N, Longstreth, W T, Weber, Frank, Lee, Yi-Chung, Tsushima, Yoshito, Alphs, Hannah, Ladd, Susanne C, Warlow, Charles, Wardlaw, Joanna M, Al-Shahi Salman, Rustam
Publicado em 2009

PRRT2 Mutations in Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions in a Taiwanese Cohort

Por Lee, Yi-Chung, Lee, Ming-Jen, Yu, Hsiang-Yu, Chen, Chien, Hsu, Chang-Hung, Lin, Kon-Ping, Liao, Kwong-Kum, Chang, Ming-Hong, Liao, Yi-Chu, Soong, Bing-Wen
Publicado em 2012

Connectivity Features for Identifying Cognitive Impairment in Presymptomatic Carotid Stenosis

Por Lin, Chun-Jen, Tu, Pei-Chi, Chern, Chang-Ming, Hsiao, Fu-Jung, Chang, Feng-Chi, Cheng, Hsien-Lin, Tang, Chih-Wei, Lee, Yi-Chung, Chen, Wei-Ta, Lee, I-Hui
Publicado em 2014

Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary Neuropathy

Por Hsiao, Cheng-Tsung, Tsai, Pei-Chien, Lin, Chou-Ching, Liu, Yo-Tsen, Huang, Yen-Hua, Liao, Yi-Chu, Huang, Han-Wei, Lin, Kon-Ping, Soong, Bing-Wen, Lee, Yi-Chung
Publicado no PLoS One (2016)