B
Bing-Wen Soong
Researcher at Taipei Veterans General Hospital
Publications - 144
Citations - 5378
Bing-Wen Soong is an academic researcher from Taipei Veterans General Hospital. The author has contributed to research in topics: Spinocerebellar ataxia & Ataxia. The author has an hindex of 39, co-authored 141 publications receiving 4776 citations. Previous affiliations of Bing-Wen Soong include Taipei Medical University & National Institutes of Health.
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Journal ArticleDOI
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia New diagnostic criteria
Michiko K. Bruno,Mark Hallett,Katrina Gwinn-Hardy,B. Sorensen,Elaine Considine,S. Tucker,David A. Lynch,Katherine D. Mathews,Kathryn J. Swoboda,Juliette Harris,Bing-Wen Soong,Tetsuo Ashizawa,Joseph Jankovic,D. Renner,Ying-Hui Fu,Louis J. Ptáček +15 more
TL;DR: The diagnosis of idiopathic paroxysmal kinesigenic dyskinesia (PKD) can be made based on historical features, and the diagnostic scheme may allow better focus in the search for the PKD gene(s).
Journal Article
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia
Michiko K. Bruno,Mark Hallett,Katrina Gwinn-Hardy,B. Sorensen,Elaine Considine,S. Tucker,David A. Lynch,Katherine D. Mathews,Kathryn J. Swoboda,Juliette Harris,Bing-Wen Soong,Tetsuo Ashizawa,Joseph Jankovic,David Renner,Ying-Hui Fu,Louis J. Ptáček +15 more
TL;DR: In this article, the authors proposed the following diagnostic criteria for idiopathic paroxysmal kinesigenic dyskinesia (PKD): identified trigger for the attacks (sudden movements), short duration of attacks (<1 minute), lack of loss of consciousness or pain during attacks, antiepileptic drug responsiveness, exclusion of other organic diseases, and age at onset between 1 and 20 years if there is no family history.
Journal ArticleDOI
Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions
Hsien Yang Lee,Yong Huang,Yong Huang,Nadine Bruneau,Patrice Roll,Elisha D.O. Roberson,Mark Hermann,Emily Quinn,Emily Quinn,James W. Maas,Robert H. Edwards,Tetsuo Ashizawa,Betül Baykan,Kailash P. Bhatia,Susan B. Bressman,Michiko K. Bruno,Michiko K. Bruno,Ewout R. Brunt,Roberto Caraballo,Bernard Echenne,Natalio Fejerman,Steve Frucht,Christina A. Gurnett,Edouard Hirsch,Henry Houlden,Joseph Jankovic,Wei Ling Lee,David A. Lynch,Shehla Mohammed,Ulrich Müller,Mark Nespeca,David Renner,Jacques Rochette,Gabrielle Rudolf,Shinji Saiki,Bing-Wen Soong,Bing-Wen Soong,Kathryn J. Swoboda,Sam Tucker,Nicholas W. Wood,Michael G. Hanna,Anne M. Bowcock,Pierre Szepetowski,Ying-Hui Fu,Louis J. Ptáček,Louis J. Ptáček +45 more
TL;DR: Four truncating mutations involving the gene PRRT2 in the vast majority of well-characterized families with PKD/IC are identified, leading ultimately to neuronal hyperexcitability that manifests in vivo as PKd/IC.
Journal ArticleDOI
Increased oxidative damage and mitochondrial abnormalities in the peripheral blood of Huntington's disease patients.
Chiung-Mei Chen,Yih-Ru Wu,Mei-Ling Cheng,Jun-Liang Liu,Yu-May Lee,Po-Wei Lee,Bing-Wen Soong,Daniel Tsun-Yee Chiu +7 more
TL;DR: Results indicate means to suppress oxidative damage or to restore mitochondrial functions may be beneficial to HD patients and plasma MDA may be used as a potential biomarker to test treatment efficacy in the future, if confirmed in a larger, longitudinal study.
Journal ArticleDOI
Clinical spectrum of Niemann‐Pick disease type C
John K. Fink,M. R. Filling-Katz,J. Sokol,D. G. Cogan,A. Pikus,Barbara C. Sonies,Bing-Wen Soong,Peter G. Pentchev,M E Comly,Roscoe O. Brady,Norman W. Barton +10 more
TL;DR: Analysis of the neurologic symptomatology in 22 patients with Niemann-Pick disease type C revealed 3 phenotypes: an early-onset, rapidly progressive form associated with severe hepatic dysfunction and psychomotor delay during infancy and later associated with dementia and, variably, seizures and extrapyramidal deficits.