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Raffaele Ferrari

Showing results (71-80 of 89) with videos related to

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Journal of Alzheimer'S Disease : JAD|January 28, 2017
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal DementiaRaffaele Ferrari, Mario Grassi, Francesca Graziano, et al.
Plos Medicine|January 30, 2018
Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studiesIris Broce, Celeste M Karch, Natalie Wen, et al.
Plos Medicine|January 10, 2018
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studiesIris Broce, Celeste M Karch, Natalie Wen, et al.
Neurobiology of Aging|July 9, 2015
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaRaffaele Ferrari, Mario Grassi, Erika Salvi, et al.
Nature|May 20, 2021
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Faiza Javad, Warren Emmett, et al.
Acta Neuropathologica|March 9, 2017
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementiaJennifer S Yokoyama, Celeste M Karch, Chun C Fan, et al.
Neurobiology of Aging|December 8, 2019
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's diseaseIrene Rosas, Carmen Martínez, Jordi Clarimón, et al.
Neurobiology of Aging|September 25, 2020
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementiaIrene Rosas, Carmen Martínez, Eliecer Coto, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Brain : a Journal of Neurology|October 23, 2021
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degenerationMathieu Barbier, Agnès Camuzat, Khalid El Hachimi, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Journal of Alzheimer'S Disease : JAD|January 28, 2017
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal DementiaRaffaele Ferrari, Mario Grassi, Francesca Graziano, et al.
Plos Medicine|January 30, 2018
Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studiesIris Broce, Celeste M Karch, Natalie Wen, et al.
Plos Medicine|January 10, 2018
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studiesIris Broce, Celeste M Karch, Natalie Wen, et al.
Neurobiology of Aging|July 9, 2015
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaRaffaele Ferrari, Mario Grassi, Erika Salvi, et al.
Nature|May 20, 2021
MIR-NATs repress MAPT translation and aid proteostasis in neurodegenerationRoberto Simone, Faiza Javad, Warren Emmett, et al.
Acta Neuropathologica|March 9, 2017
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementiaJennifer S Yokoyama, Celeste M Karch, Chun C Fan, et al.
Neurobiology of Aging|December 8, 2019
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's diseaseIrene Rosas, Carmen Martínez, Jordi Clarimón, et al.
Neurobiology of Aging|September 25, 2020
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementiaIrene Rosas, Carmen Martínez, Eliecer Coto, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Brain : a Journal of Neurology|October 23, 2021
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degenerationMathieu Barbier, Agnès Camuzat, Khalid El Hachimi, et al.
Pageof 9