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L Woltjer

Showing results (111-120 of 130) with videos related to

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Nature Communications|May 28, 2016
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystoniaKarin Tuschl, Esther Meyer, Leonardo E Valdivia, et al.
Journal of Neuropathology and Experimental Neurology|April 11, 2012
Correlation of Alzheimer disease neuropathologic changes with cognitive status: a review of the literaturePeter T Nelson, Irina Alafuzoff, Eileen H Bigio, et al.
Brain : a Journal of Neurology|August 24, 2018
The human brainome: network analysis identifies HSPA2 as a novel Alzheimer’s disease targetVladislav A Petyuk, Rui Chang, Manuel Ramirez-Restrepo, et al.
Acta Neuropathologica|May 25, 2026
Neocortical tau burden determines the degree of cognitive impairment in individuals with Braak stage V neurofibrillary degenerationTimothy E Richardson, Jonathan Cherry, Shrishtee Kandoi, et al.
Acta Neuropathologica|October 29, 2014
Primary age-related tauopathy (PART): a common pathology associated with human agingJohn F Crary, John Q Trojanowski, Julie A Schneider, et al.
Acta Neuropathologica|April 29, 2014
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathologyPeter T Nelson, Steven Estus, Erin L Abner, et al.
Journal of Neuropathology and Experimental Neurology|December 28, 2020
Early Selective Vulnerability of the CA2 Hippocampal Subfield in Primary Age-Related TauopathyJamie M Walker, Timothy E Richardson, Kurt Farrell, 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.
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.
Acta Neuropathologica|November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathyKurt Farrell, SoongHo Kim, Natalia Han, et al.
Pageof 13

Showing results (111-120 of 130) with videos related to

Sort By:
Pageof 13
Nature Communications|May 28, 2016
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystoniaKarin Tuschl, Esther Meyer, Leonardo E Valdivia, et al.
Journal of Neuropathology and Experimental Neurology|April 11, 2012
Correlation of Alzheimer disease neuropathologic changes with cognitive status: a review of the literaturePeter T Nelson, Irina Alafuzoff, Eileen H Bigio, et al.
Brain : a Journal of Neurology|August 24, 2018
The human brainome: network analysis identifies HSPA2 as a novel Alzheimer’s disease targetVladislav A Petyuk, Rui Chang, Manuel Ramirez-Restrepo, et al.
Acta Neuropathologica|May 25, 2026
Neocortical tau burden determines the degree of cognitive impairment in individuals with Braak stage V neurofibrillary degenerationTimothy E Richardson, Jonathan Cherry, Shrishtee Kandoi, et al.
Acta Neuropathologica|October 29, 2014
Primary age-related tauopathy (PART): a common pathology associated with human agingJohn F Crary, John Q Trojanowski, Julie A Schneider, et al.
Acta Neuropathologica|April 29, 2014
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathologyPeter T Nelson, Steven Estus, Erin L Abner, et al.
Journal of Neuropathology and Experimental Neurology|December 28, 2020
Early Selective Vulnerability of the CA2 Hippocampal Subfield in Primary Age-Related TauopathyJamie M Walker, Timothy E Richardson, Kurt Farrell, 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.
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.
Acta Neuropathologica|November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathyKurt Farrell, SoongHo Kim, Natalia Han, et al.
Pageof 13