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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.
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.
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