A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan

por Fung, Hon-Chung, Chen, Chiung-Mei, Hardy, John, Singleton, Andrew B, Wu, Yih-Ru
Publicado 2006

Polymorphisms of ACMSD-TMEM163, MCCC1, and BCKDK-STX1B Are Not Associated with Parkinson's Disease in Taiwan

por Chang, Kuo-Hsuan, Chen, Chiung-Mei, Chen, Yi-Chun, Fung, Hon-Chung, Wu, Yih-Ru
Publicado 2019

Fibroblast Growth Factor 20 Gene Polymorphism in Parkinson’s Disease in Asian Population: A Meta-Analysis

por Chiang, Han-Lin, Wu, Yih-Ru, Chen, Yi-Chun, Fung, Hon-Chung, Chen, Chiung-Mei
Publicado 2021

Polymorphisms of Interleukin-6 and Interleukin-8 Are Not Associated with Parkinson’s Disease in Taiwan

por Liu, Tsai-Wei, Wu, Yih-Ru, Chen, Yi-Chun, Fung, Hon-Chung, Chen, Chiung-Mei
Publicado 2021

STK39, But Not BST1, HLA-DQB1, and SPPL2B Polymorphism, Is Associated With Han-Chinese Parkinson's Disease in Taiwan

por Chang, Kuo-Hsuan, Wu, Yih-Ru, Chen, Yi-Chun, Fung, Hon-Chung, Lee-Chen, Guey-Jen, Chen, Chiung-Mei
Publicado 2015

Digit symbol substitution test score and hyperhomocysteinemia in older adults

por Hsu, Wen-Chuin, Chu, Yi-Chuan, Fung, Hon-Chung, Wai, Yau-Yau, Wang, Jiun-Jie, Lee, Jiann-Der, Chen, Yi-Chun
Publicado 2016

Association of AXIN1 With Parkinson’s Disease in a Taiwanese Population

por Fang, Hwa-Shin, Chao, Chih-Ying, Wang, Chun-Chieh, Fan, Wen-Lang, Huang, Po-Jung, Fung, Hon-Chung, Wu, Yih-Ru
Publicado 2022

The correlation of small fiber neuropathy with pain intensity and age in patients with Fabry's disease: A cross sectional study within a large Taiwanese family

por Liao, Ming-Feng, Hsu, Jung-Lung, Fung, Hon-Chung, Kuo, Hung-Chou, Chu, Chun-Che, Chang, Hong-Shiu, Lyu, Rong-Kuo, Ro, Long-Sun
Publicado 2022

Tract-Based Spatial Statistics: Application to Mild Cognitive Impairment

por Wai, Yau-Yau, Hsu, Wen-Chuin, Fung, Hon-Chung, Lee, Jiann-Der, Chan, Hsiao-Lung, Tsai, Ming-Lun, Lin, Yu-Chun, Wu, Yih-Ru, Ying, Leslie, Wang, Jiun-Jie
Publicado 2014

Sex dimorphism of cortical water diffusion in normal aging measured by magnetic resonance imaging

por Ng, Shu-Hang, Hsu, Wen-Chiun, Wai, Yau-Yau, Lee, Jiann-Der, Chan, Hsiao-Lung, Chen, Yao-Liang, Fung, Hon-Chung, Wu, Yih-Ru, Tsai, Ming-Lun, Wang, Jiun-Jie
Publicado 2013

CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan

por Chang, Chun-Wei, Hsu, Peng-Wei, Wei, Kuo-Chen, Chang, Chia-Wen, Fung, Hon-Chung, Hsih, Mo-Song, Hsu, Wen-Chuin, Ro, Long-Sun, Chang, Chen-Nen, Wang, Jiun-Jie, Wu, Yih-Ru, Chen, Sien-Tsong
Publicado 2019

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

por Momeni, Parastoo, Schymick, Jennifer, Jain, Shushant, Cookson, Mark R, Cairns, Nigel J, Greggio, Elisa, Greenway, Matthew J, Berger, Stephen, Pickering-Brown, Stuart, Chiò, Adriano, Fung, Hon Chung, Holtzman, David M, Huey, Edward D, Wassermann, Eric M, Adamson, Jennifer, Hutton, Michael L, Rogaeva, Ekaterina, St George-Hyslop, Peter, Rothstein, Jeffrey D, Hardiman, Orla, Grafman, Jordan, Singleton, Andrew, Hardy, John, Traynor, Bryan J
Publicado 2006

Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans

por van de Leemput, Joyce, Chandran, Jayanth, Knight, Melanie A, Holtzclaw, Lynne A, Scholz, Sonja, Cookson, Mark R, Houlden, Henry, Gwinn-Hardy, Katrina, Fung, Hon-Chung, Lin, Xian, Hernandez, Dena, Simon-Sanchez, Javier, Wood, Nick W, Giunti, Paola, Rafferty, Ian, Hardy, John, Storey, Elsdon, Gardner, R. J. McKinlay, Forrest, Susan M, Fisher, Elizabeth M. C, Russell, James T, Cai, Huaibin, Singleton, Andrew B
Publicado 2007