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David Pellerin

Showing results (1-10 of 55) with videos related to

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Platelets|June 30, 2017
Platelets as a surrogate disease model of neurodevelopmental disorders: Insights from Fragile X SyndromeDavid Pellerin, Audrey Lortie, François Corbin
Cureus|June 14, 2024
A Case of Non-ketotic Hyperglycemic Hemichorea and Fahr SyndromeRebecca Oksenhendler, David Pellerin, Ahmad Almutlaq
American Journal of Medical Genetics. Part A|September 27, 2014
Effect of lovastatin on behavior in children and adults with fragile X syndrome: an open-label studyArtuela Çaku, David Pellerin, Paméla Bouvier, et al.
Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals|April 9, 2016
Lovastatin corrects ERK pathway hyperactivation in fragile X syndrome: potential of platelet's signaling cascades as new outcome measures in clinical trialsDavid Pellerin, Artuela Çaku, Mathieu Fradet, et al.
Journal of Neurology|September 27, 2023
Update on leukodystrophies and developing trialsGiorgia Ceravolo, Kristina Zhelcheska, Violetta Squadrito, et al.
Clinical and Translational Medicine|January 27, 2024
Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxiaDavid Pellerin, Matt C Danzi, Mathilde Renaud, et al.
Parkinsonism & Related Disorders|July 7, 2025
FGF14 (GAA∙TTC) repeat expansion-related ataxia SCA27B is common in Northern FinlandLaura Kytövuori, David Pellerin, Mikko Kärppä, et al.
Frontiers in Neurology|March 16, 2019
Rheumatoid Meningitis Presenting With Acute Parkinsonism and Protracted Non-convulsive Seizures: An Unusual Case Presentation and Review of Treatment StrategiesDavid Pellerin, Michael Wodkowski, Marie-Christine Guiot, et al.
Current Neurology and Neuroscience Reports|January 17, 2025
Recent Advances in the Genetics of Ataxias: An Update on Novel Autosomal Dominant Repeat ExpansionsDavid Pellerin, Pablo Iruzubieta, Isaac R L Xu, et al.
Cerebellum (London, England)|May 7, 2026
Identification of FGF14 GAA Expansions in Polish Patients with Undiagnosed Cerebellar Ataxia - A Preliminary StudyMarta Matlawska, Karolina Ziora-Jakutowicz, Marie-Josee Dicaire, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Platelets|June 30, 2017
Platelets as a surrogate disease model of neurodevelopmental disorders: Insights from Fragile X SyndromeDavid Pellerin, Audrey Lortie, François Corbin
Cureus|June 14, 2024
A Case of Non-ketotic Hyperglycemic Hemichorea and Fahr SyndromeRebecca Oksenhendler, David Pellerin, Ahmad Almutlaq
American Journal of Medical Genetics. Part A|September 27, 2014
Effect of lovastatin on behavior in children and adults with fragile X syndrome: an open-label studyArtuela Çaku, David Pellerin, Paméla Bouvier, et al.
Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals|April 9, 2016
Lovastatin corrects ERK pathway hyperactivation in fragile X syndrome: potential of platelet's signaling cascades as new outcome measures in clinical trialsDavid Pellerin, Artuela Çaku, Mathieu Fradet, et al.
Journal of Neurology|September 27, 2023
Update on leukodystrophies and developing trialsGiorgia Ceravolo, Kristina Zhelcheska, Violetta Squadrito, et al.
Clinical and Translational Medicine|January 27, 2024
Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxiaDavid Pellerin, Matt C Danzi, Mathilde Renaud, et al.
Parkinsonism & Related Disorders|July 7, 2025
FGF14 (GAA∙TTC) repeat expansion-related ataxia SCA27B is common in Northern FinlandLaura Kytövuori, David Pellerin, Mikko Kärppä, et al.
Frontiers in Neurology|March 16, 2019
Rheumatoid Meningitis Presenting With Acute Parkinsonism and Protracted Non-convulsive Seizures: An Unusual Case Presentation and Review of Treatment StrategiesDavid Pellerin, Michael Wodkowski, Marie-Christine Guiot, et al.
Current Neurology and Neuroscience Reports|January 17, 2025
Recent Advances in the Genetics of Ataxias: An Update on Novel Autosomal Dominant Repeat ExpansionsDavid Pellerin, Pablo Iruzubieta, Isaac R L Xu, et al.
Cerebellum (London, England)|May 7, 2026
Identification of FGF14 GAA Expansions in Polish Patients with Undiagnosed Cerebellar Ataxia - A Preliminary StudyMarta Matlawska, Karolina Ziora-Jakutowicz, Marie-Josee Dicaire, et al.
Pageof 6