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Matthew C Baker

Showing results (71-80 of 122) with videos related to

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Rheumatology and Therapy|March 17, 2026
Efficacy and Safety of Obexelimab to Treat IgG4-Related Disease: Protocol for a Global, Randomized, Placebo-Controlled TrialEmma L Culver, Matthew C Baker, Emanuel Della-Torre, et al.
Journal of Alzheimer'S Disease : JAD|May 14, 2023
Comparison of Clinical, Genetic, and Pathologic Features of Limbic and Diffuse Transactive Response DNA-Binding Protein 43 Pathology in Alzheimer's Disease Neuropathologic SpectrumArenn F Carlos, Mary M Machulda, Matthew H Rutledge, et al.
Annals of Clinical and Translational Neurology|August 27, 2019
Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutationsNobutaka Sakae, Shanu F Roemer, Kevin F Bieniek, et al.
Journal of Neurology|January 23, 2014
Progranulin-associated PiB-negative logopenic primary progressive aphasiaKeith A Josephs, Joseph R Duffy, Edythe A Strand, et al.
Molecular Neurodegeneration|December 21, 2024
Targeted long-read sequencing to quantify methylation of the C9orf72 repeat expansionEvan Udine, NiCole A Finch, Mariely DeJesus-Hernandez, et al.
Archives of Neurology|September 12, 2012
Frontotemporal dementia in a Brazilian kindred with the c9orf72 mutationLeonel T Takada, Maria Lucia V Pimentel, Mariely Dejesus-Hernandez, et al.
Parkinsonism & Related Disorders|December 22, 2023
The MAPT p.E342K and p.R406W mutations are associated with progressive supranuclear palsy with atypical featuresNegin Badihian, Farwa Ali, Hugo Botha, et al.
Acta Neuropathologica|April 29, 2015
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degenerationMasataka Nakamura, Kevin F Bieniek, Wen-Lang Lin, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 3, 2013
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementiaMarka van Blitterswijk, Matthew C Baker, Kevin F Bieniek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 31, 2017
Cognitive impairment in progressive supranuclear palsy is associated with tau burdenShunsuke Koga, Adam Parks, Koji Kasanuki, et al.
Pageof 13

Showing results (71-80 of 122) with videos related to

Sort By:
Pageof 13
Rheumatology and Therapy|March 17, 2026
Efficacy and Safety of Obexelimab to Treat IgG4-Related Disease: Protocol for a Global, Randomized, Placebo-Controlled TrialEmma L Culver, Matthew C Baker, Emanuel Della-Torre, et al.
Journal of Alzheimer'S Disease : JAD|May 14, 2023
Comparison of Clinical, Genetic, and Pathologic Features of Limbic and Diffuse Transactive Response DNA-Binding Protein 43 Pathology in Alzheimer's Disease Neuropathologic SpectrumArenn F Carlos, Mary M Machulda, Matthew H Rutledge, et al.
Annals of Clinical and Translational Neurology|August 27, 2019
Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutationsNobutaka Sakae, Shanu F Roemer, Kevin F Bieniek, et al.
Journal of Neurology|January 23, 2014
Progranulin-associated PiB-negative logopenic primary progressive aphasiaKeith A Josephs, Joseph R Duffy, Edythe A Strand, et al.
Molecular Neurodegeneration|December 21, 2024
Targeted long-read sequencing to quantify methylation of the C9orf72 repeat expansionEvan Udine, NiCole A Finch, Mariely DeJesus-Hernandez, et al.
Archives of Neurology|September 12, 2012
Frontotemporal dementia in a Brazilian kindred with the c9orf72 mutationLeonel T Takada, Maria Lucia V Pimentel, Mariely Dejesus-Hernandez, et al.
Parkinsonism & Related Disorders|December 22, 2023
The MAPT p.E342K and p.R406W mutations are associated with progressive supranuclear palsy with atypical featuresNegin Badihian, Farwa Ali, Hugo Botha, et al.
Acta Neuropathologica|April 29, 2015
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degenerationMasataka Nakamura, Kevin F Bieniek, Wen-Lang Lin, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 3, 2013
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementiaMarka van Blitterswijk, Matthew C Baker, Kevin F Bieniek, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 31, 2017
Cognitive impairment in progressive supranuclear palsy is associated with tau burdenShunsuke Koga, Adam Parks, Koji Kasanuki, et al.
Pageof 13