Search research articles
Contact Us
Filters
Showing results (1-10 of 55) with videos related to
Page
of 6
Sort By:
Platelets
|
June 30, 2017
Platelets as a surrogate disease model of neurodevelopmental disorders: Insights from Fragile X Syndrome
David Pellerin, Audrey Lortie, François Corbin
Cureus
|
June 14, 2024
A Case of Non-ketotic Hyperglycemic Hemichorea and Fahr Syndrome
Rebecca 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 study
Artuela 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 trials
David Pellerin, Artuela Çaku, Mathieu Fradet, et al.
Journal of Neurology
|
September 27, 2023
Update on leukodystrophies and developing trials
Giorgia Ceravolo, Kristina Zhelcheska, Violetta Squadrito, et al.
Clinical and Translational Medicine
|
January 27, 2024
Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia
David 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 Finland
Laura 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 Strategies
David 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 Expansions
David 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 Study
Marta Matlawska, Karolina Ziora-Jakutowicz, Marie-Josee Dicaire, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 55) with videos related to
Sort By:
Page
of 6
Platelets
|
June 30, 2017
Platelets as a surrogate disease model of neurodevelopmental disorders: Insights from Fragile X Syndrome
David Pellerin, Audrey Lortie, François Corbin
Cureus
|
June 14, 2024
A Case of Non-ketotic Hyperglycemic Hemichorea and Fahr Syndrome
Rebecca 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 study
Artuela 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 trials
David Pellerin, Artuela Çaku, Mathieu Fradet, et al.
Journal of Neurology
|
September 27, 2023
Update on leukodystrophies and developing trials
Giorgia Ceravolo, Kristina Zhelcheska, Violetta Squadrito, et al.
Clinical and Translational Medicine
|
January 27, 2024
Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia
David 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 Finland
Laura 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 Strategies
David 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 Expansions
David 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 Study
Marta Matlawska, Karolina Ziora-Jakutowicz, Marie-Josee Dicaire, et al.
Page
of 6