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

Andrew B Singleton

Showing results (51-60 of 397) with videos related to

Pageof 40
Sort By:
Parkinsonism & Related Disorders|June 29, 2016
Juvenile onset Parkinsonism with "pure nigral" degeneration and POLG1 mutationShyamal H Mehta, Dennis W Dickson, John C Morgan, et al.
The International Journal of Neuroscience|June 18, 2013
Variability in clinical phenotypes of heterozygous and homozygous cases of Parkin-related Parkinson's diseaseAmanda J Thompson, Sonja W Scholz, Andrew B Singleton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2018
Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locusCornelis Blauwendraat, Jose M Bras, Mike A Nalls, et al.
Neurobiology of Aging|January 21, 2014
Susceptibility loci for pigmentation and melanoma in relation to Parkinson's diseaseJing Dong, Jianjun Gao, Michael Nalls, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Genome-wide meta-analysis of CSF biomarkers in Alzheimer's disease and Parkinson's disease cohortsMichael Ta, Cornelis Blauwendraat, Tarek Antar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 14, 2015
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)Mike A Nalls, Margaux F Keller, Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2023
Genome-Wide Meta-Analysis of Cerebrospinal Fluid Biomarkers in Alzheimer's Disease and Parkinson's Disease CohortsMichael Ta, Cornelis Blauwendraat, Tarek Antar, et al.
Journal of the Neurological Sciences|September 7, 2021
Longitudinal risk factors for developing depressive symptoms in Parkinson's diseaseTarek Antar, Huw R Morris, Faraz Faghri, et al.
Neurobiology of Aging|October 5, 2014
Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansionsSonja W Scholz, Elisa Majounie, Tamas Revesz, et al.
Neuroscience Letters|November 1, 2005
Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in TaiwanHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
Pageof 40

Showing results (51-60 of 397) with videos related to

Sort By:
Pageof 40
Parkinsonism & Related Disorders|June 29, 2016
Juvenile onset Parkinsonism with "pure nigral" degeneration and POLG1 mutationShyamal H Mehta, Dennis W Dickson, John C Morgan, et al.
The International Journal of Neuroscience|June 18, 2013
Variability in clinical phenotypes of heterozygous and homozygous cases of Parkin-related Parkinson's diseaseAmanda J Thompson, Sonja W Scholz, Andrew B Singleton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2018
Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locusCornelis Blauwendraat, Jose M Bras, Mike A Nalls, et al.
Neurobiology of Aging|January 21, 2014
Susceptibility loci for pigmentation and melanoma in relation to Parkinson's diseaseJing Dong, Jianjun Gao, Michael Nalls, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Genome-wide meta-analysis of CSF biomarkers in Alzheimer's disease and Parkinson's disease cohortsMichael Ta, Cornelis Blauwendraat, Tarek Antar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 14, 2015
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)Mike A Nalls, Margaux F Keller, Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2023
Genome-Wide Meta-Analysis of Cerebrospinal Fluid Biomarkers in Alzheimer's Disease and Parkinson's Disease CohortsMichael Ta, Cornelis Blauwendraat, Tarek Antar, et al.
Journal of the Neurological Sciences|September 7, 2021
Longitudinal risk factors for developing depressive symptoms in Parkinson's diseaseTarek Antar, Huw R Morris, Faraz Faghri, et al.
Neurobiology of Aging|October 5, 2014
Multiple system atrophy is not caused by C9orf72 hexanucleotide repeat expansionsSonja W Scholz, Elisa Majounie, Tamas Revesz, et al.
Neuroscience Letters|November 1, 2005
Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in TaiwanHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
Pageof 40