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Journal of the Chinese Medical Association : JCMA|May 12, 2015
Acute simultaneous multiple lacunar infarcts as the initial presentation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyCheng-Tsung Hsiao, Yun-Chung Chen, Yo-Tsen Liu, et al.Pediatric Neurology|May 19, 2007
A novel ABCD1 gene mutation in a Chinese-Taiwanese patient with adrenomyeloneuropathyYo-Tsen Liu, Kang-Hsu Lin, Bing-Wen Soong, et al.Journal of Neurology|August 22, 2009
Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in TaiwanNai-Fang Chi, Yi-Chung Lee, Yi-Chun Lu, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 23, 2003
Prolonged cortical relay time of long latency reflex and central motor conduction in patients with spinocerebellar ataxia type 6Yi-Chung Lee, Jen-Tse Chen, Kwong-Kum Liao, et al.Parkinsonism & Related Disorders|December 29, 2018
Comparable progression of spinocerebellar ataxias between Caucasians and ChineseYi-Cheng Lin, Yi-Chung Lee, Ting-Yi Hsu, et al.Journal of the Neurological Sciences|December 4, 2014
C9ORF72 repeat expansion is not a significant cause of late onset cerebellar ataxia syndromeCheng-Tsung Hsiao, Pei-Chien Tsai, Yi-Chu Liao, et al.Clinical Biochemistry|May 27, 2010
Val-9Ala and Ile+58Thr polymorphism of MnSOD in Parkinson's diseaseVinchi Wang, Shao-Yuan Chen, Tzu-Chao Chuang, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 18, 2013
Disrupted cerebellar connectivity reduces whole-brain network efficiency in multiple system atrophyChia-Feng Lu, Bing-Wen Soong, Hsiu-Mei Wu, et al.Journal of the Neurological Sciences|January 22, 2013
Polymorphic Ala-allele carriers at residue 1170 of HER2 associated with Parkinson's diseaseVinchi Wang, Tzu-Chao Chuang, Ming-Ching Kao, et al.Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|October 3, 2003
Congenital myotonic dystrophy: report of one caseYi-Hsin Liao, Whey-Chen Sue, Da-Ru Jang, et al.Pageof 13