5'-Flanking region polymorphism of the neuronal nitric oxide synthase gene with Parkinson's disease in TaiwanLO, Hsiao-Sui; HOGAN, Edward L; SOONG, Bing-Wen et al.Journal of the neurological sciences. 2002, Vol 194, Num 1, pp 11-13, issn 0022-510XArticle

Dentatorubropallidoluysian atrophy in ChineseLEE, I-Hui; SOONG, Bing-Wen; LU, Yi-Chun et al.Archives of neurology (Chicago). 2001, Vol 58, Num 11, pp 1905-1908, issn 0003-9942Article

Topographic brain mapping of the international cooperative ataxia rating scale : A positron emission tomography studyWANG, Po-Shan; LIU, Ren-Shyan; YANG, Bang-Hung et al.Journal of neurology. 2007, Vol 254, Num 6, pp 722-728, issn 0340-5354, 7 p.Article

Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of Spinocerebellar ataxia type 6SOONG, Bing-Wen; LU, Yi-Chun; CHOO, Kong-Bung et al.Archives of neurology (Chicago). 2001, Vol 58, Num 7, pp 1105-1109, issn 0003-9942Article

Use of diffusion tensor imaging to identify similarities and differences between cerebellar and Parkinsonism forms of multiple system atrophyWANG, Po-Shan; WU, Hsiu-Mei; LIN, Ching-Po et al.Neuroradiology (Berlin. Print). 2011, Vol 53, Num 7, pp 471-481, issn 0028-3940, 11 p.Article

Regional patterns of cerebral glucose metabolism in spinocerebellar ataxia type 2, 3 and 6 : A voxel-based FDG-positron emission tomography analysisWANG, Po-Shan; LIU, Ren-Shyan; YANG, Bang-Hung et al.Journal of neurology. 2007, Vol 254, Num 7, pp 838-845, issn 0340-5354, 8 p.Article

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome lp21-q23CHUNG, Ming-Yi; LU, Yi-Chun; CHENG, Nai-Chia et al.Brain. 2003, Vol 126, pp 1293-1299, issn 0006-8950, 7 p., 6Article

Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on TaiwanLEE, Yi-Chung; LU, Yi-Chun; CHANG, Ming-Hon et al.Journal of the neurological sciences. 2007, Vol 254, Num 1-2, pp 65-68, issn 0022-510X, 4 p.Article

Prolonged cortical relay time of long latency reflex and central motor conduction in patients with spinocerebellar ataxia type 6LEE, Yi-Chung; CHEN, Jen-Tse; LIAO, Kwong-Kum et al.Clinical neurophysiology. 2003, Vol 114, Num 3, pp 458-462, issn 1388-2457, 5 p.Article

Spinocerebellar ataxia 35: Novel mutations in TGM6 with clinical and genetic characterizationGUO, Yuh-Cherng; LIN, Juei-Jueng; LIAO, Yi-Chu et al.Neurology. 2014, Vol 83, Num 17, pp 1554-1561, issn 0028-3878, 8 p.Article

Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in TaiwanCHI, Nai-Fang; LEE, Yi-Chung; LU, Yi-Chun et al.Journal of neurology. 2010, Vol 257, Num 2, pp 191-197, issn 0340-5354, 7 p.Article

Polymorphism distribution of prion protein codon 117, 129 and 171 in TaiwanWANG, Kaw-Chen; WANG, Vinchi; SUN, Ming-Chieh et al.European journal of epidemiology. 2007, Vol 22, Num 4, pp 257-261, issn 0393-2990, 5 p.Article

Metabolic characterization of Spinocerebellar ataxia type 6SOONG, Bing-Wen; LIU, Ren-Shyan; WU, Liang-Chih et al.Archives of neurology (Chicago). 2001, Vol 58, Num 2, pp 300-304, issn 0003-9942Article

Creutzfeldt-Jakob disease : heat shock protein 70 mRNA levels in mononuclear blood cells and clinical studySHYU, Woei-Cherng; KAO, Ming-Ching; CHOU, Wei-Yuan et al.Journal of neurology. 2000, Vol 247, Num 12, pp 929-934, issn 0340-5354Article

Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: Clinical implicationsSHAN, Din-E; LIU, Ren-Shyan; SUN, Chen-Ming et al.Movement disorders. 2004, Vol 19, Num 11, pp 1357-1360, issn 0885-3185, 4 p.Article

Comparison of Cerebellar Ataxias: A Three-Year Prospective Longitudinal AssessmentLEE, Yi-Chung; LIAO, Yi-Chu; WANG, Po-Shan et al.Movement disorders. 2011, Vol 26, Num 11, pp 2081-2087, issn 0885-3185, 7 p.Article

A novel ABCD1 gene mutation in a chinese-taiwanese patient with adrenomyeloneuropathyLIU, Yo-Tsen; LIN, Kang-Hsu; SOONG, Bing-Wen et al.Pediatric neurology. 2007, Vol 36, Num 5, pp 348-350, issn 0887-8994, 3 p.Article

Polymorphic Ala-allele carriers at residue 1170 of HER2 associated with Parkinson's diseaseVINCHI WANG; CHUANG, Tzu-Chao; KAO, Ming-Ching et al.Journal of the neurological sciences. 2013, Vol 325, Num 1-2, pp 115-119, issn 0022-510X, 5 p.Article

Median nerve motor conduction velocity is concordant with myelin protein zero gene mutationLEE, Yi-Chung; SOONG, Bing-Wen; LIU, Yo-Tsen et al.Journal of neurology. 2005, Vol 252, Num 2, pp 151-155, issn 0340-5354, 5 p.Article

Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonismSHAN, Din-E; SOONG, Bing-Wen; SUN, Chen-Ming et al.Annals of neurology. 2001, Vol 50, Num 6, pp 812-815, issn 0364-5134Article

Val-9Ala and Ile + 58Thr polymorphism of MnSOD in Parkinson's diseaseVINCHI WANG; CHEN, Shao-Yuan; CHUANG, Tzu-Chao et al.Clinical biochemistry. 2010, Vol 43, Num 12, pp 979-982, issn 0009-9120, 4 p.Article

Depletion of mitochondrial DNA in leukocytes of patients with poly-Q diseasesLIU, Chin-San; CHENG, Wen-Ling; KUO, Shou-Jen et al.Journal of the neurological sciences. 2008, Vol 264, Num 1-2, pp 18-21, issn 0022-510X, 4 p.Article

Myelin protein zero gene mutations in Taiwanese patients with Charcot-Marie-Tooth disease type 1LEE, Yi-Chung; SOONG, Bing-Wen; LIN, Kon-Ping et al.Journal of the neurological sciences. 2004, Vol 219, Num 1-2, pp 95-100, issn 0022-510X, 6 p.Article

Congenital myotonic dystrophy: Report of one caseLIAO, Yi-Hsin; SUE, Whey-Chen; JANG, Da-Ru et al.Acta paediatrica taiwanica. 2003, Vol 44, Num 3, pp 155-157, issn 1608-8115, 3 p.Article

Dysregulation of C/EBPα by mutant huntingtin causes the urea cycle deficiency in huntington's diseaseCHIANG, Ming-Chang; CHEN, Hui-Mei; WU, Jer-Yuarn et al.Human molecular genetics (Print). 2007, Vol 16, Num 5, pp 483-498, issn 0964-6906, 16 p.Article