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Manabu Funayama

Showing results (21-30 of 98) with videos related to

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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.
Annals of Neurology|May 10, 2005
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 familyManabu Funayama, Kazuko Hasegawa, Etsuro Ohta, 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.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, JapanHiroyuki Tomiyama, Yasumasa Kokubo, Ryogen Sasaki, 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.
Journal of Neuroscience Methods|April 3, 2010
A rotarod test for evaluation of motor skill learningHiromi Shiotsuki, Kenji Yoshimi, Yasushi Shimo, et al.
Frontiers in Neurology|October 29, 2020
Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's DiseaseKensuke Daida, Manabu Funayama, Yuanzhe Li, et al.
Neurobiology of Aging|February 18, 2016
FBXO7 mutations in Parkinson's disease and multiple system atrophySilvio Conedera, Hulya Apaydin, Yuanzhe Li, et al.
Neuroscience Letters|July 20, 2010
No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patientsLin Li, Manabu Funayama, Hiroyuki Tomiyama, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2012
A case of α-synuclein gene duplication presenting with head-shaking movementsKaori Itokawa, Takeshi Sekine, Manabu Funayama, et al.
Pageof 10

Showing results (21-30 of 98) with videos related to

Sort By:
Pageof 10
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.
Annals of Neurology|May 10, 2005
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 familyManabu Funayama, Kazuko Hasegawa, Etsuro Ohta, 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.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, JapanHiroyuki Tomiyama, Yasumasa Kokubo, Ryogen Sasaki, 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.
Journal of Neuroscience Methods|April 3, 2010
A rotarod test for evaluation of motor skill learningHiromi Shiotsuki, Kenji Yoshimi, Yasushi Shimo, et al.
Frontiers in Neurology|October 29, 2020
Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's DiseaseKensuke Daida, Manabu Funayama, Yuanzhe Li, et al.
Neurobiology of Aging|February 18, 2016
FBXO7 mutations in Parkinson's disease and multiple system atrophySilvio Conedera, Hulya Apaydin, Yuanzhe Li, et al.
Neuroscience Letters|July 20, 2010
No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patientsLin Li, Manabu Funayama, Hiroyuki Tomiyama, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2012
A case of α-synuclein gene duplication presenting with head-shaking movementsKaori Itokawa, Takeshi Sekine, Manabu Funayama, et al.
Pageof 10