Splice isoform-specific suppression of the Ca(V)2.1 variant underlying Spinocerebellar ataxia type 6

Por Tsou, Wei-Ling, Soong, Bing-Wen, Paulson, Henry L., Rodríguez-Lebrón, Edgardo
Publicado em 2011

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

Association between Proton Magnetic Resonance Spectroscopy Measurements and CAG Repeat Number in Patients with Spinocerebellar Ataxias 2, 3, or 6

Por Wang, Po-Shan, Chen, Hung-Chieh, Wu, Hsiu-Mei, Lirng, Jiing-Feng, Wu, Yu-Te, Soong, Bing-Wen
Publicado em 2012

Differences between Spinocerebellar Ataxias and Multiple System Atrophy-Cerebellar Type on Proton Magnetic Resonance Spectroscopy

Por Lirng, Jiing-Feng, Wang, Po-Shan, Chen, Hung-Chieh, Soong, Bing-Wen, Guo, Wan Yuo, Wu, Hsiu-Mei, Chang, Cheng-Yen
Publicado em 2012

Change in the Cortical Complexity of Spinocerebellar Ataxia Type 3 Appears Earlier than Clinical Symptoms

Por Wang, Tzu-Yun, Jao, Chii-Wen, Soong, Bing-Wen, Wu, Hsiu-Mei, Shyu, Kuo-Kai, Wang, Po-Shan, Wu, Yu-Te
Publicado no PLoS One (2015)

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)

CAG repeat length does not associate with the rate of cerebellar degeneration in spinocerebellar ataxia type 3

Por Huang, Shang-Ran, Wu, Yu-Te, Jao, Chii-Wen, Soong, Bing-Wen, Lirng, Jiing-Feng, Wu, Hsiu-Mei, Wang, Po-Shan
Publicado no Neuroimage Clin (2016)

The merit of proton magnetic resonance spectroscopy in the longitudinal assessment of spinocerebellar ataxias and multiple system atrophy-cerebellar type

Por Chen, Hung-Chieh, Lirng, Jiing-Feng, Soong, Bing-Wen, Guo, Wan Yuo, Wu, Hsiu-Mei, Chen, Clayton Chi-Chang, Chang, Cheng-Yen
Publicado no Cerebellum Ataxias (2014)

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)

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

High Protein Diet and Huntington's Disease

Por Chen, Chiung-Mei, Lin, Yow-Sien, Wu, Yih-Ru, Chen, Pei, Tsai, Fuu-Jen, Yang, Chueh-Lien, Tsao, Ya-Tzu, Chang, Wen, Hsieh, I-Shan, Chern, Yijuang, Soong, Bing-Wen
Publicado no PLoS One (2015)

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)

Treatment of Spinocerebellar Ataxia with Mesenchymal Stem Cells: A Phase I/IIa Clinical Study

Por Tsai, Yun-An, Liu, Ren-Shyan, Lirng, Jiing-Feng, Yang, Bang-Hung, Chang, Chin-Hao, Wang, Yi-Chen, Wu, Yu-Shan, Ho, Jennifer Hui-Chun, Lee, Oscar K., Soong, Bing-Wen
Publicado no Cell Transplant (2017)

Clinical and biophysical characterization of 19 GJB1 mutations

Por Tsai, Pei‐Chien, Yang, De‐Ming, Liao, Yi‐Chu, Chiu, Tai‐Yu, Kuo, Hung‐Chou, Su, Yu‐Ping, Guo, Yuh‐Cherng, Soong, Bing‐Wen, Lin, Kon‐Ping, Liu, Yo‐Tsen, Lee, Yi‐Chung
Publicado no Ann Clin Transl Neurol (2016)

Dysregulated brain creatine kinase is associated with hearing impairment in mouse models of Huntington disease

Por Lin, Yow-Sien, Chen, Chiung-Mei, Soong, Bing-wen, Wu, Yih-Ru, Chen, Hui-Mei, Yeh, Wen-Ying, Wu, Dai-Rong, Lin, Yi-Jun, Poon, Paul Wai-Fung, Cheng, Mei-Ling, Wang, Chih-Hung, Chern, Yijuang
Publicado em 2011

PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects

Por Liu, Yo-Tsen, Nian, Fang-Shin, Chou, Wan-Ju, Tai, Chin-Yin, Kwan, Shang-Yeong, Chen, Chien, Kuo, Pei-Wen, Lin, Po-Hsi, Chen, Chin-Yi, Huang, Chia-Wei, Lee, Yi-Chung, Soong, Bing-Wen, Tsai, Jin-Wu
Publicado no Oncotarget (2016)

Exome Sequencing Identifies GNB4 Mutations as a Cause of Dominant Intermediate Charcot-Marie-Tooth Disease

Por Soong, Bing-Wen, Huang, Yen-Hua, Tsai, Pei-Chien, Huang, Chien-Chang, Pan, Hung-Chuan, Lu, Yi-Chun, Chien, Hsin-Ju, Liu, Tze-Tze, Chang, Ming-Hong, Lin, Kon-Ping, Tu, Pang-Hsien, Kao, Lung-Sen, Lee, Yi-Chung
Publicado em 2013