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Manabu Funayama

Showing results (41-50 of 98) with videos related to

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Journal of Human Genetics|October 17, 2008
LRRK2 P755L variant in sporadic Parkinson's diseaseHiroyuki Tomiyama, Ikuko Mizuta, Yuanzhe Li, et al.
Neurobiology of Aging|February 19, 2014
Evaluation of polyglutamine repeats in autosomal dominant Parkinson's diseaseChikara Yamashita, Hiroyuki Tomiyama, Manabu Funayama, et al.
Heliyon|August 22, 2024
Genetic and clinical study of <i>PARK7</i> in Japanese Parkinson's diseaseMayu Ishiguro, Manabu Funayama, Taku Hatano, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 17, 2025
Identification of DAGLB variants in Japanese early-onset Parkinson's diseaseYue Luo, Manabu Funayama, Taku Hatano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 19, 2019
Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography featuresAya Ikeda, Hitoshi Shimada, Kenya Nishioka, et al.
Archives of Neurology|November 15, 2006
Novel mutations in the guanosine triphosphate cyclohydrolase 1 gene associated with DYT5 dystoniaEtsuro Ohta, Manabu Funayama, Hiroshi Ichinose, et al.
Neurobiology of Aging|November 29, 2016
Genotype-phenotype correlations of cysteine replacement in CADASILTakashi Matsushima, Silvio Conedera, Ryota Tanaka, et al.
Neurobiology of Aging|July 2, 2017
Homozygous alpha-synuclein p.A53V in familial Parkinson's diseaseHiroyo Yoshino, Makito Hirano, A Jon Stoessl, et al.
Human Molecular Genetics|February 25, 2021
Homeostatic p62 levels and inclusion body formation in CHCHD2 knockout miceShigeto Sato, Sachiko Noda, Satoru Torii, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 13, 2018
COQ2 variants in Parkinson's disease and multiple system atrophyMichitaka Mikasa, Kazuaki Kanai, Yuanzhe Li, et al.
Pageof 10

Showing results (41-50 of 98) with videos related to

Sort By:
Pageof 10
Journal of Human Genetics|October 17, 2008
LRRK2 P755L variant in sporadic Parkinson's diseaseHiroyuki Tomiyama, Ikuko Mizuta, Yuanzhe Li, et al.
Neurobiology of Aging|February 19, 2014
Evaluation of polyglutamine repeats in autosomal dominant Parkinson's diseaseChikara Yamashita, Hiroyuki Tomiyama, Manabu Funayama, et al.
Heliyon|August 22, 2024
Genetic and clinical study of <i>PARK7</i> in Japanese Parkinson's diseaseMayu Ishiguro, Manabu Funayama, Taku Hatano, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 17, 2025
Identification of DAGLB variants in Japanese early-onset Parkinson's diseaseYue Luo, Manabu Funayama, Taku Hatano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 19, 2019
Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography featuresAya Ikeda, Hitoshi Shimada, Kenya Nishioka, et al.
Archives of Neurology|November 15, 2006
Novel mutations in the guanosine triphosphate cyclohydrolase 1 gene associated with DYT5 dystoniaEtsuro Ohta, Manabu Funayama, Hiroshi Ichinose, et al.
Neurobiology of Aging|November 29, 2016
Genotype-phenotype correlations of cysteine replacement in CADASILTakashi Matsushima, Silvio Conedera, Ryota Tanaka, et al.
Neurobiology of Aging|July 2, 2017
Homozygous alpha-synuclein p.A53V in familial Parkinson's diseaseHiroyo Yoshino, Makito Hirano, A Jon Stoessl, et al.
Human Molecular Genetics|February 25, 2021
Homeostatic p62 levels and inclusion body formation in CHCHD2 knockout miceShigeto Sato, Sachiko Noda, Satoru Torii, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 13, 2018
COQ2 variants in Parkinson's disease and multiple system atrophyMichitaka Mikasa, Kazuaki Kanai, Yuanzhe Li, et al.
Pageof 10