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Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Clinical course of the first Asian family with Parkinsonism related to SNCA triplicationTakeshi Sekine, Hajime Kagaya, Manabu Funayama, et al.Journal of Human Genetics|January 19, 2023
Analysis of LIN28A variants in patients with Parkinson's diseaseHao Peng, Yuanzhe Li, Hiroyo Yoshino, et al.Parkinsonism & Related Disorders|June 6, 2021
Genetic analysis of ATP10B for Parkinson's disease in JapanMayu Ishiguro, Hiroyo Yoshino, Yuanzhe Li, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2010
Rapid screening of ATP13A2 variant with high-resolution melting analysisManabu Funayama, Hiroyuki Tomiyama, Ruey-Meei Wu, et al.Neuroscience Letters|May 12, 2009
Mutation analysis for DJ-1 in sporadic and familial parkinsonism: screening strategy in parkinsonismHiroyuki Tomiyama, Yuanzhe Li, Hiroyo Yoshino, et al.Neurobiology of Aging|October 16, 2013
Clinicogenetic study of GBA mutations in patients with familial Parkinson's diseaseYuanzhe Li, Takeshi Sekine, Manabu Funayama, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|December 13, 2016
Mutation screening of PLA2G6 in Japanese patients with early onset dystonia-parkinsonismChikara Yamashita, Manabu Funayama, Yuanzhe Li, et al.Neurobiology of Aging|October 5, 2019
Mutation analysis of LRP10 in Japanese patients with familial Parkinson's disease, progressive supranuclear palsy, and frontotemporal dementiaKensuke Daida, Kenya Nishioka, Yuanzhe Li, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|February 5, 2017
Neuromelanin MRI is useful for monitoring motor complications in Parkinson's and PARK2 diseaseTaku Hatano, Ayami Okuzumi, Koji Kamagata, et al.Acta Neuropathologica Communications|October 19, 2018
Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutationsMasashi Takanashi, Manabu Funayama, Eiji Matsuura, et al.Pageof 8