Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Manabu Funayama

Showing results (11-20 of 98) with videos related to

Pageof 10
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|February 7, 2012
Pseudo-heterozygous rearrangement mutation of parkinManabu Funayama, Hiroyo Yoshino, Yuanzhe Li, et al.
Parkinsonism & Related Disorders|January 7, 2018
Genetic analysis of TMEM230 in Japanese patients with familial Parkinson's diseaseSilvio A Conedera, Yuanzhe Li, 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.
Eneurologicalsci|January 17, 2022
A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the <i>SPG11</i> geneKensuke Daida, Yosuke Nishioka, Yuanzhe Li, 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|September 7, 2010
Clinical course of the first Asian family with Parkinsonism related to SNCA triplicationTakeshi Sekine, Hajime Kagaya, Manabu Funayama, 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.
International Journal of Pediatric Otorhinolaryngology|November 30, 2010
Prevalence of GJB2 causing recessive profound non-syndromic deafness in Japanese childrenChieri Hayashi, Manabu Funayama, Yuanzhe Li, 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.
The American Journal of Pathology|October 23, 2016
Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient MiceShigeto Sato, Masato Koike, Manabu Funayama, et al.
Pageof 10

Showing results (11-20 of 98) with videos related to

Sort By:
Pageof 10
Movement Disorders : Official Journal of the Movement Disorder Society|February 7, 2012
Pseudo-heterozygous rearrangement mutation of parkinManabu Funayama, Hiroyo Yoshino, Yuanzhe Li, et al.
Parkinsonism & Related Disorders|January 7, 2018
Genetic analysis of TMEM230 in Japanese patients with familial Parkinson's diseaseSilvio A Conedera, Yuanzhe Li, 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.
Eneurologicalsci|January 17, 2022
A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the <i>SPG11</i> geneKensuke Daida, Yosuke Nishioka, Yuanzhe Li, 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|September 7, 2010
Clinical course of the first Asian family with Parkinsonism related to SNCA triplicationTakeshi Sekine, Hajime Kagaya, Manabu Funayama, 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.
International Journal of Pediatric Otorhinolaryngology|November 30, 2010
Prevalence of GJB2 causing recessive profound non-syndromic deafness in Japanese childrenChieri Hayashi, Manabu Funayama, Yuanzhe Li, 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.
The American Journal of Pathology|October 23, 2016
Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient MiceShigeto Sato, Masato Koike, Manabu Funayama, et al.
Pageof 10