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Cyril Pottier

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Brain : a Journal of Neurology|November 22, 2014
PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion diseaseCyril Pottier, Matt Baker, Dennis W Dickson, et al.
Journal of Neurochemistry|March 25, 2016
Genetics of FTLD: overview and what else we can expect from genetic studiesCyril Pottier, Thomas A Ravenscroft, Monica Sanchez-Contreras, et al.
Annals of Neurology|February 4, 2026
Understanding Neurodegenerative Diseases From the -Omics Perspective: Lessons LearntLaura Ibanez, Cyril Pottier, Aleksandra Beric, et al.
Mycoses|November 2, 2021
Multilocus sequence typing of strains from the Cryptococcus gattii species complex from different continentsVirginie Bellet, Frédéric Roger, Donika Krasteva, et al.
Journal of Alzheimer'S Disease : JAD|November 3, 2011
Amyloid-β protein precursor gene expression in alzheimer's disease and other conditionsCyril Pottier, David Wallon, Anne Rovelet Lecrux, et al.
Journal of Alzheimer'S Disease : JAD|February 6, 2013
TREM2 R47H variant as a risk factor for early-onset Alzheimer's diseaseCyril Pottier, David Wallon, Stephane Rousseau, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 28, 2019
Clinicopathologic correlations in a family with a <i>TBK1</i> mutation presenting as primary progressive aphasia and primary lateral sclerosisVeronica Hirsch-Reinshagen, Omar A Alfaify, Ging-Yuek R Hsiung, et al.
Neurogenetics|April 29, 2014
Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcificationGaël Nicolas, Anne-Claire Richard, Cyril Pottier, et al.
Journal of Molecular Neuroscience : MN|March 8, 2014
PDGFB partial deletion: a new, rare mechanism causing brain calcification with leukoencephalopathyGaël Nicolas, Anne Rovelet-Lecrux, Cyril Pottier, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 28, 2025
Evaluating pathogenicity of variants of unknown significance in APP, PSEN1, and PSEN2Jacob A Marsh, Guangming Huang, Kevin Bowling, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Brain : a Journal of Neurology|November 22, 2014
PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion diseaseCyril Pottier, Matt Baker, Dennis W Dickson, et al.
Journal of Neurochemistry|March 25, 2016
Genetics of FTLD: overview and what else we can expect from genetic studiesCyril Pottier, Thomas A Ravenscroft, Monica Sanchez-Contreras, et al.
Annals of Neurology|February 4, 2026
Understanding Neurodegenerative Diseases From the -Omics Perspective: Lessons LearntLaura Ibanez, Cyril Pottier, Aleksandra Beric, et al.
Mycoses|November 2, 2021
Multilocus sequence typing of strains from the Cryptococcus gattii species complex from different continentsVirginie Bellet, Frédéric Roger, Donika Krasteva, et al.
Journal of Alzheimer'S Disease : JAD|November 3, 2011
Amyloid-β protein precursor gene expression in alzheimer's disease and other conditionsCyril Pottier, David Wallon, Anne Rovelet Lecrux, et al.
Journal of Alzheimer'S Disease : JAD|February 6, 2013
TREM2 R47H variant as a risk factor for early-onset Alzheimer's diseaseCyril Pottier, David Wallon, Stephane Rousseau, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 28, 2019
Clinicopathologic correlations in a family with a <i>TBK1</i> mutation presenting as primary progressive aphasia and primary lateral sclerosisVeronica Hirsch-Reinshagen, Omar A Alfaify, Ging-Yuek R Hsiung, et al.
Neurogenetics|April 29, 2014
Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcificationGaël Nicolas, Anne-Claire Richard, Cyril Pottier, et al.
Journal of Molecular Neuroscience : MN|March 8, 2014
PDGFB partial deletion: a new, rare mechanism causing brain calcification with leukoencephalopathyGaël Nicolas, Anne Rovelet-Lecrux, Cyril Pottier, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 28, 2025
Evaluating pathogenicity of variants of unknown significance in APP, PSEN1, and PSEN2Jacob A Marsh, Guangming Huang, Kevin Bowling, et al.
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