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Rosa Rademakers

Showing results (21-30 of 421) with videos related to

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Neuro-Degenerative Diseases|March 4, 2010
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderlyDennis W Dickson, Matthew Baker, Rosa Rademakers
Brain Pathology (Zurich, Switzerland)|May 12, 2007
Progressive supranuclear palsy: pathology and geneticsDennis W Dickson, Rosa Rademakers, Michael L Hutton
Current Opinion in Neurology|November 20, 2012
How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?Marka van Blitterswijk, Mariely DeJesus-Hernandez, Rosa Rademakers
Journal of Molecular Neuroscience : MN|June 1, 2011
Human genetics as a tool to identify progranulin regulatorsAlexandra M Nicholson, NiCole A Finch, Rosa Rademakers
Alzheimer'S Research & Therapy|January 27, 2012
Progranulin axis and recent developments in frontotemporal lobar degenerationAlexandra M Nicholson, Jennifer Gass, Leonard Petrucelli, et al.
Annals of the New York Academy of Sciences|January 6, 2015
Frontotemporal dementia: a bridge between dementia and neuromuscular diseaseAdeline S L Ng, Rosa Rademakers, Bruce L Miller
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.
BMC Bioinformatics|March 27, 2025
Methylmap: visualization of modified nucleotides for large cohort sizesElise Coopman, Svenn D'Hert, Rosa Rademakers, 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.
Frontiers in Neurology|April 20, 2023
Case report: TMEM106B haplotype alters penetrance of GRN mutation in frontotemporal dementia familyJolien Perneel, Masood Manoochehri, Edward D Huey, et al.
Pageof 43

Showing results (21-30 of 421) with videos related to

Sort By:
Pageof 43
Neuro-Degenerative Diseases|March 4, 2010
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderlyDennis W Dickson, Matthew Baker, Rosa Rademakers
Brain Pathology (Zurich, Switzerland)|May 12, 2007
Progressive supranuclear palsy: pathology and geneticsDennis W Dickson, Rosa Rademakers, Michael L Hutton
Current Opinion in Neurology|November 20, 2012
How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?Marka van Blitterswijk, Mariely DeJesus-Hernandez, Rosa Rademakers
Journal of Molecular Neuroscience : MN|June 1, 2011
Human genetics as a tool to identify progranulin regulatorsAlexandra M Nicholson, NiCole A Finch, Rosa Rademakers
Alzheimer'S Research & Therapy|January 27, 2012
Progranulin axis and recent developments in frontotemporal lobar degenerationAlexandra M Nicholson, Jennifer Gass, Leonard Petrucelli, et al.
Annals of the New York Academy of Sciences|January 6, 2015
Frontotemporal dementia: a bridge between dementia and neuromuscular diseaseAdeline S L Ng, Rosa Rademakers, Bruce L Miller
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.
BMC Bioinformatics|March 27, 2025
Methylmap: visualization of modified nucleotides for large cohort sizesElise Coopman, Svenn D'Hert, Rosa Rademakers, 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.
Frontiers in Neurology|April 20, 2023
Case report: TMEM106B haplotype alters penetrance of GRN mutation in frontotemporal dementia familyJolien Perneel, Masood Manoochehri, Edward D Huey, et al.
Pageof 43