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Acta Neurologica Taiwanica|July 9, 2011
Foodborne botulinum type E intoxication associated with dried bean curd: first case report in TaiwanLung-Shiang Lai, Yi-Mei Wang, Chin-Hsien LinNPJ Parkinson'S Disease|July 11, 2026
Plasma pTau217 and pTau231 predict progression to dementia in Parkinson's disease: a prospective longitudinal studyCheng-Hsuan Li, Ting-Wen Cheng, Chin-Hsien LinJournal of Parkinson'S Disease|December 24, 2019
Integrated Plasma and Neuroimaging Biomarkers Associated with Motor and Cognition Severity in Parkinson's DiseaseChih-Hao Chen, Bo-Ching Lee, Chin-Hsien LinJournal of Clinical Apheresis|October 20, 2004
Plasmapheresis in acute disseminated encephalomyelitisChin-Hsien Lin, Jiann-Shing Jeng, Ping-Keung YipMovement Disorders Clinical Practice|October 27, 2018
Acute Levodopa Challenge Test in Patients with de novo Parkinson's Disease: Data from the DeNoPa CohortSebastian Schade, Friederike Sixel-Döring, Jens Ebentheuer, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 14, 2023
Extracellular Vesicles for the Diagnosis of Parkinson's Disease: Systematic Review and Meta-AnalysisMary Xylaki, Avika Chopra, Sandrina Weber, et al.Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|February 11, 2015
REM Sleep Behavioral Events and DreamingMaria-Lucia Muntean, Claudia Trenkwalder, Arthur S Walters, et al.Stem Cell Research|October 17, 2020
Reprogramming of a human induced pluripotent stem cell (iPSC) line from a patient with neurodegeneration with brain iron accumulation (NBIA) harboring a novel frameshift mutation in C19orf12 geneHan-Yi Lin, Chih-Hsin Ou-Yang, Chin-Hsien LinStem Cell Research|July 22, 2022
Generation of a human induced pluripotent stem cell line NTUHi002-A from a patient with aceruloplasminemia harboring a homozygous splicing mutation c.607+1 delG in CP geneChih-Hsin Ou-Yang, Han-I Lin, Chin-Hsien LinStem Cell Research|March 8, 2024
Generation of a human induced pluripotent stem cell line NTUHi004-A from a patient with Leigh syndrome harboring a homozygous missense mutation c.836 T > G (p.Met279Arg) in NDUFAF5 geneChih-Hsin Ou-Yang, Pin-Shiuan Chen, Chin-Hsien LinPageof 53