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Mathieu Anheim

Showing results (71-80 of 189) with videos related to

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American Journal of Human Genetics|October 13, 2015
A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar AtaxiaMarie Coutelier, Iulia Blesneac, Arnaud Monteil, et al.
Journal of Neurodevelopmental Disorders|April 9, 2015
Erratum: Emerging topics in FXTASDeborah A Hall, Rachael C Birch, Mathieu Anheim, et al.
Neurobiology of Aging|June 5, 2012
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?Suzanne Lesage, Christel Condroyer, Stephan Klebe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 19, 2026
Divergent Cerebello-Cortical Network Responses to Emotional Stress in Myoclonus DystoniaClément Tarrano, Cécile Galléa, Manon Gomes, et al.
Open Forum Infectious Diseases|July 15, 2020
Coronavirus Disease 2019: Associated Multiple Organ DamageOlivier Collange, Charles Tacquard, Xavier Delabranche, et al.
JAMA Neurology|August 21, 2013
SYNE1 mutations in autosomal recessive cerebellar ataxiaAnne Noreau, Cynthia V Bourassa, Anna Szuto, 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.
Movement Disorders : Official Journal of the Movement Disorder Society|May 6, 2020
The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal MyoclonusJuliette Piard, Matthieu Béreau, Wenshu XiangWei, et al.
European Radiology|May 13, 2022
MRI dedicated to the emergency department for diplopia or dizziness: a cost-effectiveness analysisSabrina Kepka, Kevin Zarca, François Lersy, et al.
Critical Care (London, England)|August 11, 2020
Delirium and encephalopathy in severe COVID-19: a cohort analysis of ICU patientsJulie Helms, Stéphane Kremer, Hamid Merdji, et al.
Pageof 19

Showing results (71-80 of 189) with videos related to

Sort By:
Pageof 19
American Journal of Human Genetics|October 13, 2015
A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar AtaxiaMarie Coutelier, Iulia Blesneac, Arnaud Monteil, et al.
Journal of Neurodevelopmental Disorders|April 9, 2015
Erratum: Emerging topics in FXTASDeborah A Hall, Rachael C Birch, Mathieu Anheim, et al.
Neurobiology of Aging|June 5, 2012
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?Suzanne Lesage, Christel Condroyer, Stephan Klebe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 19, 2026
Divergent Cerebello-Cortical Network Responses to Emotional Stress in Myoclonus DystoniaClément Tarrano, Cécile Galléa, Manon Gomes, et al.
Open Forum Infectious Diseases|July 15, 2020
Coronavirus Disease 2019: Associated Multiple Organ DamageOlivier Collange, Charles Tacquard, Xavier Delabranche, et al.
JAMA Neurology|August 21, 2013
SYNE1 mutations in autosomal recessive cerebellar ataxiaAnne Noreau, Cynthia V Bourassa, Anna Szuto, 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.
Movement Disorders : Official Journal of the Movement Disorder Society|May 6, 2020
The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal MyoclonusJuliette Piard, Matthieu Béreau, Wenshu XiangWei, et al.
European Radiology|May 13, 2022
MRI dedicated to the emergency department for diplopia or dizziness: a cost-effectiveness analysisSabrina Kepka, Kevin Zarca, François Lersy, et al.
Critical Care (London, England)|August 11, 2020
Delirium and encephalopathy in severe COVID-19: a cohort analysis of ICU patientsJulie Helms, Stéphane Kremer, Hamid Merdji, et al.
Pageof 19