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Matthew P Frosch

Showing results (271-280 of 290) with videos related to

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The Lancet. Neurology|July 16, 2022
The Boston criteria version 2.0 for cerebral amyloid angiopathy: a multicentre, retrospective, MRI-neuropathology diagnostic accuracy studyAndreas Charidimou, Gregoire Boulouis, Matthew P Frosch, et al.
Acta Neuropathologica|June 3, 2025
Immunohistochemical evaluation of a trial of gantenerumab or solanezumab in dominantly inherited Alzheimer diseaseCharles D Chen, Erin E Franklin, Yan Li, et al.
Cerebellum (London, England)|October 3, 2022
Clinical Trial-Ready Patient Cohorts for Multiple System Atrophy: Coupling Biospecimen and iPSC Banking to Longitudinal Deep-PhenotypingAlain Ndayisaba, Ariana T Pitaro, Andrew S Willett, et al.
Cell|July 23, 2019
An Integrative Model of Cellular States, Plasticity, and Genetics for GlioblastomaCyril Neftel, Julie Laffy, Mariella G Filbin, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Archives of Neurology|April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationAlice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System AtrophyFranziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Human Molecular Genetics|May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesGiovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Acta Neuropathologica|November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathyKurt Farrell, SoongHo Kim, Natalia Han, et al.
Pageof 29

Showing results (271-280 of 290) with videos related to

Sort By:
Pageof 29
The Lancet. Neurology|July 16, 2022
The Boston criteria version 2.0 for cerebral amyloid angiopathy: a multicentre, retrospective, MRI-neuropathology diagnostic accuracy studyAndreas Charidimou, Gregoire Boulouis, Matthew P Frosch, et al.
Acta Neuropathologica|June 3, 2025
Immunohistochemical evaluation of a trial of gantenerumab or solanezumab in dominantly inherited Alzheimer diseaseCharles D Chen, Erin E Franklin, Yan Li, et al.
Cerebellum (London, England)|October 3, 2022
Clinical Trial-Ready Patient Cohorts for Multiple System Atrophy: Coupling Biospecimen and iPSC Banking to Longitudinal Deep-PhenotypingAlain Ndayisaba, Ariana T Pitaro, Andrew S Willett, et al.
Cell|July 23, 2019
An Integrative Model of Cellular States, Plasticity, and Genetics for GlioblastomaCyril Neftel, Julie Laffy, Mariella G Filbin, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Archives of Neurology|April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationAlice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System AtrophyFranziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Human Molecular Genetics|May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesGiovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Acta Neuropathologica|November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathyKurt Farrell, SoongHo Kim, Natalia Han, et al.
Pageof 29