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

von Lo, Yang-Ching, Liao, Kwong-Kum, Lee, Yi-Chung, Soong, Bing-Wen
Veröffentlicht 2011

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

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

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

von Jih, Kang-Yang, Tsai, Pei-Chien, Tsai, Yu-Shuen, Liao, Yi-Chu, Lee, Yi-Chung
Veröffentlicht in Neurol Genet (2020)

Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias

von Hsiao, Cheng-Tsung, Liu, Yo-Tsen, Liao, Yi-Chu, Hsu, Ting-Yi, Lee, Yi-Chung, Soong, Bing-Wen
Veröffentlicht in PLoS One (2017)

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

von Hsiao, Cheng-Tsung, Liu, Yo-Tsen, Liao, Yi-Chu, Hsu, Ting-Yi, Lee, Yi-Chung, Soong, Bing-Wen
Veröffentlicht in PLoS One (2018)

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

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

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

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

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

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

Spinocerebellar ataxia type 36 in the Han Chinese

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

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

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

Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan

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

Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

von Chou, Cheng‐Ta, Soong, Bing‐Wen, Lin, Kon‐Ping, Tsai, Yu‐Shuen, Jih, Kang‐Yang, Liao, Yi‐Chu, Lee, Yi‐Chung
Veröffentlicht in 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...

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

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

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

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

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

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia

von 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
Veröffentlicht in PLoS One (2017)

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

von 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
Veröffentlicht 2009

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

von 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
Veröffentlicht 2012

Connectivity Features for Identifying Cognitive Impairment in Presymptomatic Carotid Stenosis

von 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
Veröffentlicht 2014

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

von 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
Veröffentlicht in PLoS One (2016)