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

Mathieu Anheim

Showing results (61-70 of 189) with videos related to

Pageof 19
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|November 25, 2021
A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex DystoniaAmjad Khan, Anne Molitor, Sylvain Mayeur, et al.
Human Molecular Genetics|October 16, 2010
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's diseaseSuzanne Lesage, Mathieu Anheim, Christel Condroyer, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|August 7, 2019
Sleep in <i>ADCY5</i>-Related Dyskinesia: Prolonged Awakenings Caused by Abnormal MovementsAurélie Méneret, Emmanuel Roze, Jean-Baptiste Maranci, et al.
European Journal of Human Genetics : EJHG|December 17, 2015
Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2)Claire Guissart, Nathalie Drouot, Ibrahim Oncel, et al.
Frontiers in Neurology|January 31, 2018
Health-Related Quality of Life Is Severely Affected in Primary Orthostatic TremorLucie Maugest, Eavan M McGovern, Katia Mazalovic, et al.
JAMA Neurology|June 19, 2018
Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement DisordersSolveig Montaut, Christine Tranchant, Nathalie Drouot, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 11, 2020
Loss-of-Function Mutations in NR4A2 Cause Dopa-Responsive Dystonia ParkinsonismThomas Wirth, Louise Laure Mariani, Gaber Bergant, et al.
Journal of Neurology|May 28, 2016
XPR1 mutations are a rare cause of primary familial brain calcificationMathieu Anheim, Uriel López-Sánchez, Donatella Giovannini, et al.
Journal of Neurodevelopmental Disorders|February 3, 2015
Emerging topics in FXTASDeborah A Hall, Rachael C Birch, Mathieu Anheim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2015
The impact of rare variants in FUS in essential tremorFranziska Hopfner, Giovanni Stevanin, Stefanie H Müller, et al.
Pageof 19

Showing results (61-70 of 189) with videos related to

Sort By:
Pageof 19
Movement Disorders : Official Journal of the Movement Disorder Society|November 25, 2021
A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex DystoniaAmjad Khan, Anne Molitor, Sylvain Mayeur, et al.
Human Molecular Genetics|October 16, 2010
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's diseaseSuzanne Lesage, Mathieu Anheim, Christel Condroyer, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|August 7, 2019
Sleep in <i>ADCY5</i>-Related Dyskinesia: Prolonged Awakenings Caused by Abnormal MovementsAurélie Méneret, Emmanuel Roze, Jean-Baptiste Maranci, et al.
European Journal of Human Genetics : EJHG|December 17, 2015
Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2)Claire Guissart, Nathalie Drouot, Ibrahim Oncel, et al.
Frontiers in Neurology|January 31, 2018
Health-Related Quality of Life Is Severely Affected in Primary Orthostatic TremorLucie Maugest, Eavan M McGovern, Katia Mazalovic, et al.
JAMA Neurology|June 19, 2018
Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement DisordersSolveig Montaut, Christine Tranchant, Nathalie Drouot, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 11, 2020
Loss-of-Function Mutations in NR4A2 Cause Dopa-Responsive Dystonia ParkinsonismThomas Wirth, Louise Laure Mariani, Gaber Bergant, et al.
Journal of Neurology|May 28, 2016
XPR1 mutations are a rare cause of primary familial brain calcificationMathieu Anheim, Uriel López-Sánchez, Donatella Giovannini, et al.
Journal of Neurodevelopmental Disorders|February 3, 2015
Emerging topics in FXTASDeborah A Hall, Rachael C Birch, Mathieu Anheim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2015
The impact of rare variants in FUS in essential tremorFranziska Hopfner, Giovanni Stevanin, Stefanie H Müller, et al.
Pageof 19