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

par Lo, Yang-Ching, Liao, Kwong-Kum, Lee, Yi-Chung, Soong, Bing-Wen
Publié 2011

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

par Chen, Chung-Huang, Wu, Meng-Ling, Lee, Yi-Chung, Layne, Matthew D., Yet, Shaw-Fang
Publié 2010

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

par Jih, Kang-Yang, Tsai, Pei-Chien, Tsai, Yu-Shuen, Liao, Yi-Chu, Lee, Yi-Chung
Publié dans Neurol Genet (2020)

Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias

par Hsiao, Cheng-Tsung, Liu, Yo-Tsen, Liao, Yi-Chu, Hsu, Ting-Yi, Lee, Yi-Chung, Soong, Bing-Wen
Publié dans PLoS One (2017)

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

par Hsiao, Cheng-Tsung, Liu, Yo-Tsen, Liao, Yi-Chu, Hsu, Ting-Yi, Lee, Yi-Chung, Soong, Bing-Wen
Publié dans PLoS One (2018)

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

par Hsu, Yun‐Hsin, Lin, Kon‐Ping, Guo, Yuh‐Cherng, Tsai, Yu‐Shuen, Liao, Yi‐Chu, Lee, Yi‐Chung
Publié dans Ann Clin Transl Neurol (2019)

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

par Tsai, Yu‐Shuen, Lin, Kon‐Ping, Jih, Kang‐Yang, Tsai, Pei‐Chien, Liao, Yi‐Chu, Lee, Yi‐Chung
Publié dans Ann Clin Transl Neurol (2020)

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

par Liao, Yi-Chu, Liu, Yo-Tsen, Tsai, Pei-Chien, Chang, Chia-Ching, Huang, Yen-Hua, Soong, Bing-Wen, Lee, Yi-Chung
Publié dans PLoS One (2015)

Spinocerebellar ataxia type 36 in the Han Chinese

par Lee, Yi-Chung, Tsai, Pei-Chien, Guo, Yuh-Cherng, Hsiao, Cheng-Tsung, Liu, Guan-Ting, Liao, Yi-Chu, Soong, Bing-Wen
Publié dans Neurol Genet (2016)

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

par Liao, Yi-Chu, Tsai, Pei-Chien, Lin, Thy-Sheng, Hsiao, Cheng-Tsung, Chao, Nai-Chen, Lin, Kon-Ping, Lee, Yi-Chung
Publié dans Sci Rep (2017)

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

par Chao, Hua‐Chuan, Liao, Yi‐Chu, Liu, Yo‐Tsen, Guo, Yuh‐Cherng, Chang, Fu‐Pang, Lee, Yi‐Chung, Lin, Kon‐Ping
Publié dans Ann Clin Transl Neurol (2019)

Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

par Chou, Cheng‐Ta, Soong, Bing‐Wen, Lin, Kon‐Ping, Tsai, Yu‐Shuen, Jih, Kang‐Yang, Liao, Yi‐Chu, Lee, Yi‐Chung
Publié dans 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...

par Chung, Chih‐Ping, Chen, Jiun‐Wei, Chang, Feng‐Chi, Li, Wei‐Chi, Lee, Yi‐Chung, Chen, Li‐Fen, Liao, Yi‐Chu
Publié dans J Am Heart Assoc (2020)

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

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

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

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

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia

par 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
Publié dans PLoS One (2017)

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

par 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
Publié 2009

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

par 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
Publié 2012

Connectivity Features for Identifying Cognitive Impairment in Presymptomatic Carotid Stenosis

par 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
Publié 2014

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

par 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
Publié dans PLoS One (2016)