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Journal of Neuroscience Research|October 28, 2009
Recurrent systemic infections with Streptococcus pneumoniae do not aggravate the course of experimental neurodegenerative diseasesSandra Ebert, Miriam Goos, Lena Rollwagen, et al.
Physical Therapy|October 16, 2010
Minimal detectable change of the timed "up & go" test and the dynamic gait index in people with Parkinson diseaseSheau-Ling Huang, Ching-Lin Hsieh, Ruey-Meei Wu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 1, 2015
Time trends in the prevalence and incidence of Parkinson's disease in Taiwan: A nationwide, population-based studyWeng-Ming Liu, Ruey-Meei Wu, Jou-Wei Lin, et al.
Journal of Clinical Psychopharmacology|October 5, 2013
Effects of selective serotonin reuptake inhibitors versus tricyclic antidepressants on cerebrovascular events: a nationwide population-based cohort studyYen-Chieh Lee, Chin-Hsien Lin, Min-Shung Lin, et al.
Journal of Clinical Medicine|October 19, 2019
Plasma pS129-α-Synuclein Is a Surrogate Biofluid Marker of Motor Severity and Progression in Parkinson's DiseaseChin-Hsien Lin, Huei-Chun Liu, Shieh-Yueh Yang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|March 21, 2026
Epidemiological burden of Alzheimer's and Parkinson's diseases in East Asia: A comparative review of global burden of disease estimates and national registry dataSung-Pin Fan, Po-Chen Liu, Jing-Zhong Wang, et al.
Parkinsonism & Related Disorders|August 27, 2011
Advanced Theory of Mind in patients at early stage of Parkinson's diseaseRwei-Ling Yu, Ruey-Meei Wu, Ming-Jang Chiu, et al.
Journal of Biomedical Science|June 5, 2008
LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: clinical, PET, and functional studiesChin-Hsien Lin, Kai-Yuan Tzen, Chin-Yi Yu, et al.
Neurobiology of Disease|December 24, 2024
Striatal-cortical dysconnectivity underlies somatosensory deficits in Parkinson's disease: Insights from rhythmic auditory-motor trainingCheng-Wei Huang, Hsin-Yun Tsai, Yi-Hsuan Lin, et al.
Journal of Human Genetics|January 30, 2010
A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndromeHoi-Fong Chan, Meng-Ling Chen, Jen-Jen Su, et al.
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