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Matthew C Baker

Showing results (61-70 of 122) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|April 30, 2008
Progranulin gene mutation with an unusual clinical and neuropathologic presentationChristian Wider, Ryan J Uitti, Zbigniew K Wszolek, et al.
Acta Neuropathologica Communications|July 12, 2023
Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologiesShunsuke Koga, Aya Murakami, Alexandra I Soto-Beasley, et al.
Dementia and Geriatric Cognitive Disorders|March 14, 2015
Dominant frontotemporal dementia mutations in 140 cases of primary progressive aphasia and speech apraxiaEoin P Flanagan, Matthew C Baker, Ralph B Perkerson, et al.
Acta Neuropathologica Communications|July 6, 2023
Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologiesShunsuke Koga, Aya Murakami, Alexandra I Soto-Beasley, et al.
Arthritis Care & Research|April 6, 2026
Artificial Intelligence-Aided Lung Ultrasound Detection of Interstitial Lung Disease in Systemic Sclerosis and Inflammatory MyopathyRobert M Fairchild, Mariani D Deluna, Mojtaba Fazli, et al.
Acta Neuropathologica|March 9, 2006
Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindredYasuhiko Baba, Bernardino Ghetti, Matthew C Baker, et al.
Journal of Molecular Neuroscience : MN|August 25, 2011
Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutationElise G P Dopper, Harro Seelaar, Wang Zheng Chiu, et al.
Journal of Neuropathology and Experimental Neurology|May 13, 2006
Atypical progressive supranuclear palsy with corticospinal tract degenerationKeith A Josephs, Omi Katsuse, Dayne A Beccano-Kelly, et al.
Acta Neuropathologica|October 12, 2012
Tau pathology in frontotemporal lobar degeneration with C9ORF72 hexanucleotide repeat expansionKevin F Bieniek, Melissa E Murray, Nicola J Rutherford, et al.
Journal of Neurology|August 24, 2022
Atypical Alzheimer's disease phenotypes with normal or borderline PET biomarker profilesNeha Atulkumar Singh, Jonathan Graff-Radford, Mary M Machulda, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
Movement Disorders : Official Journal of the Movement Disorder Society|April 30, 2008
Progranulin gene mutation with an unusual clinical and neuropathologic presentationChristian Wider, Ryan J Uitti, Zbigniew K Wszolek, et al.
Acta Neuropathologica Communications|July 12, 2023
Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologiesShunsuke Koga, Aya Murakami, Alexandra I Soto-Beasley, et al.
Dementia and Geriatric Cognitive Disorders|March 14, 2015
Dominant frontotemporal dementia mutations in 140 cases of primary progressive aphasia and speech apraxiaEoin P Flanagan, Matthew C Baker, Ralph B Perkerson, et al.
Acta Neuropathologica Communications|July 6, 2023
Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologiesShunsuke Koga, Aya Murakami, Alexandra I Soto-Beasley, et al.
Arthritis Care & Research|April 6, 2026
Artificial Intelligence-Aided Lung Ultrasound Detection of Interstitial Lung Disease in Systemic Sclerosis and Inflammatory MyopathyRobert M Fairchild, Mariani D Deluna, Mojtaba Fazli, et al.
Acta Neuropathologica|March 9, 2006
Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindredYasuhiko Baba, Bernardino Ghetti, Matthew C Baker, et al.
Journal of Molecular Neuroscience : MN|August 25, 2011
Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutationElise G P Dopper, Harro Seelaar, Wang Zheng Chiu, et al.
Journal of Neuropathology and Experimental Neurology|May 13, 2006
Atypical progressive supranuclear palsy with corticospinal tract degenerationKeith A Josephs, Omi Katsuse, Dayne A Beccano-Kelly, et al.
Acta Neuropathologica|October 12, 2012
Tau pathology in frontotemporal lobar degeneration with C9ORF72 hexanucleotide repeat expansionKevin F Bieniek, Melissa E Murray, Nicola J Rutherford, et al.
Journal of Neurology|August 24, 2022
Atypical Alzheimer's disease phenotypes with normal or borderline PET biomarker profilesNeha Atulkumar Singh, Jonathan Graff-Radford, Mary M Machulda, et al.
Pageof 13