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Christelle Tesson

Showing results (1-10 of 48) with videos related to

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Human Genetics|March 12, 2015
Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosologyChristelle Tesson, Jeanette Koht, Giovanni Stevanin
Movement Disorders Clinical Practice|January 23, 2025
A PARK7 Mutation-Induced Early-Onset Parkinson's Disease in a Moroccan Family: Expanding the Geographic SpectrumHicham El Otmani, Christelle Tesson, Alexis Brice, et al.
Neurogenetics|July 21, 2021
Lack of evidence for association of UQCRC1 with autosomal dominant Parkinson's disease in Caucasian familiesThomas Courtin, Christelle Tesson, Jean-Christophe Corvol, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 11, 2023
Identification of a DAGLB Mutation in a Non-Chinese Patient with Parkinson's DiseaseChristelle Tesson, Mohamed Sofiane Bouchetara, Mélanie Ferrien, et al.
The Lancet. Neurology|December 4, 2018
LRP10 in α-synucleinopathiesChristelle Tesson, Christine Brefel-Courbon, Jean-Christophe Corvol, et al.
Acta Neuropathologica|September 6, 2020
Segregation of ATP10B variants in families with autosomal recessive parkinsonismChristelle Tesson, Ebba Lohmann, David Devos, et al.
Journal of Molecular Neuroscience : MN|June 20, 2020
Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson DiseaseImane Smaili, Christelle Tesson, Wafa Regragui, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2024
Confirmation of RAB32 Ser71Arg Involvement in Parkinson's DiseaseGuillaume Cogan, Christelle Tesson, Christine Brefel-Courbon, et al.
Frontiers in Neurology|April 12, 2021
Clinical Variability of <i>SYNJ1</i>-Associated Early-Onset ParkinsonismSuzanne Lesage, Graziella Mangone, Christelle Tesson, et al.
Disease Models & Mechanisms|December 19, 2018
SUMOylation by SUMO2 is implicated in the degradation of misfolded ataxin-7 via RNF4 in SCA7 modelsMartina Marinello, Andreas Werner, Mariagiovanna Giannone, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Human Genetics|March 12, 2015
Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosologyChristelle Tesson, Jeanette Koht, Giovanni Stevanin
Movement Disorders Clinical Practice|January 23, 2025
A PARK7 Mutation-Induced Early-Onset Parkinson's Disease in a Moroccan Family: Expanding the Geographic SpectrumHicham El Otmani, Christelle Tesson, Alexis Brice, et al.
Neurogenetics|July 21, 2021
Lack of evidence for association of UQCRC1 with autosomal dominant Parkinson's disease in Caucasian familiesThomas Courtin, Christelle Tesson, Jean-Christophe Corvol, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 11, 2023
Identification of a DAGLB Mutation in a Non-Chinese Patient with Parkinson's DiseaseChristelle Tesson, Mohamed Sofiane Bouchetara, Mélanie Ferrien, et al.
The Lancet. Neurology|December 4, 2018
LRP10 in α-synucleinopathiesChristelle Tesson, Christine Brefel-Courbon, Jean-Christophe Corvol, et al.
Acta Neuropathologica|September 6, 2020
Segregation of ATP10B variants in families with autosomal recessive parkinsonismChristelle Tesson, Ebba Lohmann, David Devos, et al.
Journal of Molecular Neuroscience : MN|June 20, 2020
Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson DiseaseImane Smaili, Christelle Tesson, Wafa Regragui, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2024
Confirmation of RAB32 Ser71Arg Involvement in Parkinson's DiseaseGuillaume Cogan, Christelle Tesson, Christine Brefel-Courbon, et al.
Frontiers in Neurology|April 12, 2021
Clinical Variability of <i>SYNJ1</i>-Associated Early-Onset ParkinsonismSuzanne Lesage, Graziella Mangone, Christelle Tesson, et al.
Disease Models & Mechanisms|December 19, 2018
SUMOylation by SUMO2 is implicated in the degradation of misfolded ataxin-7 via RNF4 in SCA7 modelsMartina Marinello, Andreas Werner, Mariagiovanna Giannone, et al.
Pageof 5