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Showing results (591-600 of 621) with videos related to

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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.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Neurobiology of Aging|September 27, 2016
Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodiesCelia Kun-Rodrigues, Owen A Ross, Tatiana Orme, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 13, 2025
The Neighborhoods Study: Examining the social exposome in Alzheimer's disease and related dementiasGrace C George, Sarah A Keller, Erin Abner, et al.
Neurobiology of Aging|November 19, 2018
A comprehensive screening of copy number variability in dementia with Lewy bodiesCelia Kun-Rodrigues, Tatiana Orme, Susana Carmona, 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.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear PalsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
The Lancet. Neurology|December 22, 2017
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association studyRita Guerreiro, Owen A Ross, Celia Kun-Rodrigues, et al.
Acta Neuropathologica|December 15, 2015
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategyGabor G Kovacs, Isidro Ferrer, Lea T Grinberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal CellsHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Pageof 63

Showing results (591-600 of 621) with videos related to

Sort By:
Pageof 63
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.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Neurobiology of Aging|September 27, 2016
Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodiesCelia Kun-Rodrigues, Owen A Ross, Tatiana Orme, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 13, 2025
The Neighborhoods Study: Examining the social exposome in Alzheimer's disease and related dementiasGrace C George, Sarah A Keller, Erin Abner, et al.
Neurobiology of Aging|November 19, 2018
A comprehensive screening of copy number variability in dementia with Lewy bodiesCelia Kun-Rodrigues, Tatiana Orme, Susana Carmona, 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.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear PalsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
The Lancet. Neurology|December 22, 2017
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association studyRita Guerreiro, Owen A Ross, Celia Kun-Rodrigues, et al.
Acta Neuropathologica|December 15, 2015
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategyGabor G Kovacs, Isidro Ferrer, Lea T Grinberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal CellsHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Pageof 63