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Matt Baker

Showing results (21-30 of 88) with videos related to

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European Neurology|May 28, 2014
ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish familyJoanna Siuda, Tatiana Lewicka, Malgorzata Bujak, et al.
Psychiatry and Clinical Neurosciences|May 8, 2010
Psychometric evaluation of personality in a patient with FTDP-17Emilia J Sitek, Ewa Narozańska, Jarosław Sławek, et al.
Acta Neuropathologica|May 24, 2011
Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutationIan R A Mackenzie, Olaf Ansorge, Michael Strong, et al.
Acta Neuropsychiatrica|November 12, 2014
Unilateral neglect in a patient diagnosed with frontotemporal dementia and parkinsonism linked to chromosome 17Emilia J Sitek, Ewa Narożańska, Jarosław Sławek, et al.
Brain : a Journal of Neurology|April 26, 2023
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypesCristina T Vicente, Jolien Perneel, Sarah Wynants, et al.
Free Neuropathology|December 14, 2023
Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions in Alzheimer's diseaseKeith A Josephs, Shunsuke Koga, Nirubol Tosakulwong, et al.
Parkinsonism & Related Disorders|December 11, 2002
A family with a tau P301L mutation presenting with parkinsonismRuth H Walker, Joseph Friedman, Jill Wiener, et al.
Acta Neuropathologica|January 6, 2023
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and agingJolien Perneel, Manuela Neumann, Bavo Heeman, et al.
Acta Neuropathologica|December 17, 2022
Accumulation of TMEM106B C-terminal fragments in neurodegenerative disease and agingJolien Perneel, Manuela Neumann, Bavo Heeman, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 28, 2019
Clinicopathologic correlations in a family with a <i>TBK1</i> mutation presenting as primary progressive aphasia and primary lateral sclerosisVeronica Hirsch-Reinshagen, Omar A Alfaify, Ging-Yuek R Hsiung, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
European Neurology|May 28, 2014
ALS-FTD complex disorder due to C9ORF72 gene mutation: description of first Polish familyJoanna Siuda, Tatiana Lewicka, Malgorzata Bujak, et al.
Psychiatry and Clinical Neurosciences|May 8, 2010
Psychometric evaluation of personality in a patient with FTDP-17Emilia J Sitek, Ewa Narozańska, Jarosław Sławek, et al.
Acta Neuropathologica|May 24, 2011
Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutationIan R A Mackenzie, Olaf Ansorge, Michael Strong, et al.
Acta Neuropsychiatrica|November 12, 2014
Unilateral neglect in a patient diagnosed with frontotemporal dementia and parkinsonism linked to chromosome 17Emilia J Sitek, Ewa Narożańska, Jarosław Sławek, et al.
Brain : a Journal of Neurology|April 26, 2023
C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypesCristina T Vicente, Jolien Perneel, Sarah Wynants, et al.
Free Neuropathology|December 14, 2023
Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions in Alzheimer's diseaseKeith A Josephs, Shunsuke Koga, Nirubol Tosakulwong, et al.
Parkinsonism & Related Disorders|December 11, 2002
A family with a tau P301L mutation presenting with parkinsonismRuth H Walker, Joseph Friedman, Jill Wiener, et al.
Acta Neuropathologica|January 6, 2023
Correction to: Accumulation of TMEM106B C‑terminal fragments in neurodegenerative disease and agingJolien Perneel, Manuela Neumann, Bavo Heeman, et al.
Acta Neuropathologica|December 17, 2022
Accumulation of TMEM106B C-terminal fragments in neurodegenerative disease and agingJolien Perneel, Manuela Neumann, Bavo Heeman, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 28, 2019
Clinicopathologic correlations in a family with a <i>TBK1</i> mutation presenting as primary progressive aphasia and primary lateral sclerosisVeronica Hirsch-Reinshagen, Omar A Alfaify, Ging-Yuek R Hsiung, et al.
Pageof 9