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

Christelle Tesson

Showing results (21-30 of 48) with videos related to

Pageof 5
Sort By:
JAMA Neurology|July 12, 2016
Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic ApproachLouise-Laure Mariani, Christelle Tesson, Perrine Charles, et al.
Brain : a Journal of Neurology|May 16, 2025
Linking polygenic risk scores to dopaminergic neuron loss using neuromelanin-sensitive imagingAymeric Lanore, Rahul Gaurav, François-Xavier Lejeune, et al.
Brain : a Journal of Neurology|March 23, 2013
Interferon β induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in miceAlice Chort, Sandro Alves, Martina Marinello, et al.
Movement Disorders Clinical Practice|April 18, 2023
Detection of <i>ATXN2</i> Expansions in an Exome Dataset: An Underdiagnosed Cause of ParkinsonismFanny Casse, Thomas Courtin, Christelle Tesson, et al.
Cell Reports|November 29, 2018
The E3 Ubiquitin Ligases TRIM17 and TRIM41 Modulate α-Synuclein Expression by Regulating ZSCAN21Iréna Lassot, Stéphan Mora, Suzanne Lesage, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 23, 2025
Screening of Hidden Pathogenic Structural Variants in PRKNKensuke Daida, Guillaume Cogan, Christelle Tesson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 6, 2014
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansionMasato Obayashi, Giovanni Stevanin, Matthis Synofzik, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 23, 2020
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Human Mutation|October 17, 2017
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56Christelle M Durand, Laura Dhers, Christelle Tesson, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
JAMA Neurology|July 12, 2016
Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic ApproachLouise-Laure Mariani, Christelle Tesson, Perrine Charles, et al.
Brain : a Journal of Neurology|May 16, 2025
Linking polygenic risk scores to dopaminergic neuron loss using neuromelanin-sensitive imagingAymeric Lanore, Rahul Gaurav, François-Xavier Lejeune, et al.
Brain : a Journal of Neurology|March 23, 2013
Interferon β induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in miceAlice Chort, Sandro Alves, Martina Marinello, et al.
Movement Disorders Clinical Practice|April 18, 2023
Detection of <i>ATXN2</i> Expansions in an Exome Dataset: An Underdiagnosed Cause of ParkinsonismFanny Casse, Thomas Courtin, Christelle Tesson, et al.
Cell Reports|November 29, 2018
The E3 Ubiquitin Ligases TRIM17 and TRIM41 Modulate α-Synuclein Expression by Regulating ZSCAN21Iréna Lassot, Stéphan Mora, Suzanne Lesage, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 23, 2025
Screening of Hidden Pathogenic Structural Variants in PRKNKensuke Daida, Guillaume Cogan, Christelle Tesson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 6, 2014
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansionMasato Obayashi, Giovanni Stevanin, Matthis Synofzik, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 23, 2020
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairmentThomas Roux, Mathieu Barbier, Mélanie Papin, et al.
Human Mutation|October 17, 2017
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56Christelle M Durand, Laura Dhers, Christelle Tesson, et al.
Pageof 5