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

Jonathan Carr

Showing results (71-80 of 98) with videos related to

Pageof 10
Sort By:
Biochemical and Biophysical Research Communications|April 12, 2014
Mitochondrial impairment observed in fibroblasts from South African Parkinson's disease patients with parkin mutationsCelia van der Merwe, Ben Loos, Chrisna Swart, et al.
British Journal of Sports Medicine|November 10, 2017
Chronic inflammation is a feature of Achilles tendinopathy and ruptureStephanie Georgina Dakin, Julia Newton, Fernando O Martinez, et al.
Movement Disorders Clinical Practice|August 2, 2024
Extended Phenotype of PEX11B Pathogenic Variants: Ataxia, Tremor, and Dystonia Due to a Novel C.2T > G VariantFranclo Henning, Kireshnee Naidu, Christopher J Record, et al.
Discover Mental Health|October 20, 2023
RNA-seq analysis of gene expression profiles in posttraumatic stress disorder, Parkinson's disease and schizophrenia identifies roles for common and distinct biological pathwaysSian M J Hemmings, Patricia Swart, Jacqueline S Womersely, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 7, 2018
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disabilityDemy J S Kuipers, Jonathan Carr, Soraya Bardien, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2009
GCH1 in early-onset Parkinson's diseaseStephanie A Cobb, Christian Wider, Owen A Ross, et al.
BMC Medical Genetics|February 6, 2020
Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patientsOluwafemi G Oluwole, Helena Kuivaniemi, Shameemah Abrahams, et al.
Trials|December 24, 2017
United Kingdom Frozen Shoulder Trial (UK FROST), multi-centre, randomised, 12 month, parallel group, superiority study to compare the clinical and cost-effectiveness of Early Structured Physiotherapy versus manipulation under anaesthesia versus arthroscopic capsular release for patients referred to secondary care with a primary frozen shoulder: study protocol for a randomised controlled trialStephen Brealey, Alison L Armstrong, Andrew Brooksbank, et al.
Human Molecular Genetics|March 4, 2010
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humansSuzanne Lesage, Etienne Patin, Christel Condroyer, et al.
Brain : a Journal of Neurology|September 8, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disabilityChristina Fevga, Christelle Tesson, Ana Carreras Mascaro, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
Biochemical and Biophysical Research Communications|April 12, 2014
Mitochondrial impairment observed in fibroblasts from South African Parkinson's disease patients with parkin mutationsCelia van der Merwe, Ben Loos, Chrisna Swart, et al.
British Journal of Sports Medicine|November 10, 2017
Chronic inflammation is a feature of Achilles tendinopathy and ruptureStephanie Georgina Dakin, Julia Newton, Fernando O Martinez, et al.
Movement Disorders Clinical Practice|August 2, 2024
Extended Phenotype of PEX11B Pathogenic Variants: Ataxia, Tremor, and Dystonia Due to a Novel C.2T > G VariantFranclo Henning, Kireshnee Naidu, Christopher J Record, et al.
Discover Mental Health|October 20, 2023
RNA-seq analysis of gene expression profiles in posttraumatic stress disorder, Parkinson's disease and schizophrenia identifies roles for common and distinct biological pathwaysSian M J Hemmings, Patricia Swart, Jacqueline S Womersely, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 7, 2018
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disabilityDemy J S Kuipers, Jonathan Carr, Soraya Bardien, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2009
GCH1 in early-onset Parkinson's diseaseStephanie A Cobb, Christian Wider, Owen A Ross, et al.
BMC Medical Genetics|February 6, 2020
Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patientsOluwafemi G Oluwole, Helena Kuivaniemi, Shameemah Abrahams, et al.
Trials|December 24, 2017
United Kingdom Frozen Shoulder Trial (UK FROST), multi-centre, randomised, 12 month, parallel group, superiority study to compare the clinical and cost-effectiveness of Early Structured Physiotherapy versus manipulation under anaesthesia versus arthroscopic capsular release for patients referred to secondary care with a primary frozen shoulder: study protocol for a randomised controlled trialStephen Brealey, Alison L Armstrong, Andrew Brooksbank, et al.
Human Molecular Genetics|March 4, 2010
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humansSuzanne Lesage, Etienne Patin, Christel Condroyer, et al.
Brain : a Journal of Neurology|September 8, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disabilityChristina Fevga, Christelle Tesson, Ana Carreras Mascaro, et al.
Pageof 10