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Christelle Tesson

Showing results (11-20 of 48) with videos related to

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Annals of Clinical and Translational Neurology|May 4, 2023
PLA2G6-associated late-onset parkinsonism in a Sudanese familyYousuf Bakhit, Christelle Tesson, Mohamed O Ibrahim, et al.
NPJ Parkinson'S Disease|January 4, 2024
Proxy-analysis of the genetics of cognitive decline in Parkinson's disease through polygenic scoresJohann Faouzi, Manuela Tan, Fanny Casse, et al.
NPJ Parkinson'S Disease|October 17, 2025
Should ITSN1 be considered as a Mendelian Parkinson's disease gene? Description of three novel familiesGuillaume Cogan, Christelle Tesson, Lisa Welment, et al.
Annals of Neurology|March 11, 2023
Differences in Survival across Monogenic Forms of Parkinson's DiseaseAymeric Lanore, Fanny Casse, Christelle Tesson, et al.
Frontiers in Neurology|November 23, 2017
Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene PanelAhmed Bouhouche, Christelle Tesson, Wafaa Regragui, et al.
Human Molecular Genetics|January 11, 2019
LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's diseaseFiona Bonello, Sidi-Mohamed Hassoun, François Mouton-Liger, et al.
Human Molecular Genetics|December 24, 2016
Mitochondrial morphology and cellular distribution are altered in SPG31 patients and are linked to DRP1 hyperphosphorylationJulie Lavie, Román Serrat, Nadège Bellance, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in <i>PRKN</i> in two individuals with early-onset Parkinson's diseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2024
Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's DiseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Neurobiology of Aging|August 28, 2018
Mutation analysis of Parkinson's disease genes in a Russian data setAnton K Emelyanov, Tatiana S Usenko, Christelle Tesson, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Annals of Clinical and Translational Neurology|May 4, 2023
PLA2G6-associated late-onset parkinsonism in a Sudanese familyYousuf Bakhit, Christelle Tesson, Mohamed O Ibrahim, et al.
NPJ Parkinson'S Disease|January 4, 2024
Proxy-analysis of the genetics of cognitive decline in Parkinson's disease through polygenic scoresJohann Faouzi, Manuela Tan, Fanny Casse, et al.
NPJ Parkinson'S Disease|October 17, 2025
Should ITSN1 be considered as a Mendelian Parkinson's disease gene? Description of three novel familiesGuillaume Cogan, Christelle Tesson, Lisa Welment, et al.
Annals of Neurology|March 11, 2023
Differences in Survival across Monogenic Forms of Parkinson's DiseaseAymeric Lanore, Fanny Casse, Christelle Tesson, et al.
Frontiers in Neurology|November 23, 2017
Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene PanelAhmed Bouhouche, Christelle Tesson, Wafaa Regragui, et al.
Human Molecular Genetics|January 11, 2019
LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's diseaseFiona Bonello, Sidi-Mohamed Hassoun, François Mouton-Liger, et al.
Human Molecular Genetics|December 24, 2016
Mitochondrial morphology and cellular distribution are altered in SPG31 patients and are linked to DRP1 hyperphosphorylationJulie Lavie, Román Serrat, Nadège Bellance, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in <i>PRKN</i> in two individuals with early-onset Parkinson's diseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2024
Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's DiseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Neurobiology of Aging|August 28, 2018
Mutation analysis of Parkinson's disease genes in a Russian data setAnton K Emelyanov, Tatiana S Usenko, Christelle Tesson, et al.
Pageof 5