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

Oury Monchi

Showing results (131-140 of 154) with videos related to

Pageof 16
Sort By:
NPJ Parkinson'S Disease|December 17, 2019
Report from a multidisciplinary meeting on anxiety as a non-motor manifestation of Parkinson's diseaseGregory M Pontone, Nadeeka Dissanayka, Liana Apostolova, et al.
NPJ Parkinson'S Disease|June 19, 2020
Erratum: Author Correction: Report from a multidisciplinary meeting on anxiety as a non-motor manifestation of Parkinson's diseaseGregory M Pontone, Nadeeka Dissanayaka, Liana Apostolova, et al.
Brain : a Journal of Neurology|February 24, 2023
Mitochondrial function-associated genes underlie cortical atrophy in prodromal synucleinopathiesShady Rahayel, Christina Tremblay, Andrew Vo, et al.
Neurobiology of Aging|November 26, 2020
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's diseasePrabhjyot Saini, Uladzislau Rudakou, Eric Yu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersRichard Camicioli, Sandra E Black, Michael J Borrie, et al.
NPJ Parkinson'S Disease|April 29, 2025
LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domainSitki Cem Parlar, Konstantin Senkevich, Eric Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2026
Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's DiseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's diseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
Open neuroinformatics infrastructure ecosystem for federated multisite studiesMichelle Wang, Nikhil Bhagwat, Francesco Cremonesi, et al.
Neurobiology of Aging|May 7, 2020
Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's diseaseBouchra Ouled Amar Bencheikh, Konstantin Senkevich, Uladzislau Rudakou, et al.
Pageof 16

Showing results (131-140 of 154) with videos related to

Sort By:
Pageof 16
NPJ Parkinson'S Disease|December 17, 2019
Report from a multidisciplinary meeting on anxiety as a non-motor manifestation of Parkinson's diseaseGregory M Pontone, Nadeeka Dissanayka, Liana Apostolova, et al.
NPJ Parkinson'S Disease|June 19, 2020
Erratum: Author Correction: Report from a multidisciplinary meeting on anxiety as a non-motor manifestation of Parkinson's diseaseGregory M Pontone, Nadeeka Dissanayaka, Liana Apostolova, et al.
Brain : a Journal of Neurology|February 24, 2023
Mitochondrial function-associated genes underlie cortical atrophy in prodromal synucleinopathiesShady Rahayel, Christina Tremblay, Andrew Vo, et al.
Neurobiology of Aging|November 26, 2020
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's diseasePrabhjyot Saini, Uladzislau Rudakou, Eric Yu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersRichard Camicioli, Sandra E Black, Michael J Borrie, et al.
NPJ Parkinson'S Disease|April 29, 2025
LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domainSitki Cem Parlar, Konstantin Senkevich, Eric Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2026
Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's DiseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's diseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
Open neuroinformatics infrastructure ecosystem for federated multisite studiesMichelle Wang, Nikhil Bhagwat, Francesco Cremonesi, et al.
Neurobiology of Aging|May 7, 2020
Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's diseaseBouchra Ouled Amar Bencheikh, Konstantin Senkevich, Uladzislau Rudakou, et al.
Pageof 16