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Matt Baker

Showing results (31-40 of 88) with videos related to

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Acta Neuropathologica|December 8, 2006
Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusionsJustus C Dächsel, Owen A Ross, Ignacio F Mata, et al.
Brain : a Journal of Neurology|October 31, 2006
The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin geneIan R A Mackenzie, Matt Baker, Stuart Pickering-Brown, et al.
Acta Neuropathologica|January 10, 2012
Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9pHeather Stewart, Nicola J Rutherford, Hannah Briemberg, et al.
Neuroimage. Clinical|May 28, 2021
FDG-PET in presymptomatic C9orf72 mutation carriersKarteek Popuri, Mirza Faisal Beg, Hyunwoo Lee, et al.
Clinical Nuclear Medicine|June 30, 2025
Distinct 11C-ER176 PET Neuroinflammatory Profiles and Tau Colocalization in Progressive Apraxia of Speech With and Without Parkinson-plus SyndromeRyota Satoh, Rene L Utianski, Joseph R Duffy, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 19, 2012
Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlationEileen H Bigio, Sandra Weintraub, Rosa Rademakers, et al.
Human Mutation|March 17, 2010
De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosisMariely DeJesus-Hernandez, Jannet Kocerha, NiCole Finch, et al.
European Journal of Neurology|October 15, 2014
Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosisChristina Sundal, Matt Baker, Virginija Karrenbauer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutationStuart Pickering-Brown, Matt Baker, Thomas Bird, et al.
BMC Genomics|October 29, 2011
Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutationsJannet Kocerha, Naomi Kouri, Matt Baker, et al.
Pageof 9

Showing results (31-40 of 88) with videos related to

Sort By:
Pageof 9
Acta Neuropathologica|December 8, 2006
Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusionsJustus C Dächsel, Owen A Ross, Ignacio F Mata, et al.
Brain : a Journal of Neurology|October 31, 2006
The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin geneIan R A Mackenzie, Matt Baker, Stuart Pickering-Brown, et al.
Acta Neuropathologica|January 10, 2012
Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9pHeather Stewart, Nicola J Rutherford, Hannah Briemberg, et al.
Neuroimage. Clinical|May 28, 2021
FDG-PET in presymptomatic C9orf72 mutation carriersKarteek Popuri, Mirza Faisal Beg, Hyunwoo Lee, et al.
Clinical Nuclear Medicine|June 30, 2025
Distinct 11C-ER176 PET Neuroinflammatory Profiles and Tau Colocalization in Progressive Apraxia of Speech With and Without Parkinson-plus SyndromeRyota Satoh, Rene L Utianski, Joseph R Duffy, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 19, 2012
Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlationEileen H Bigio, Sandra Weintraub, Rosa Rademakers, et al.
Human Mutation|March 17, 2010
De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosisMariely DeJesus-Hernandez, Jannet Kocerha, NiCole Finch, et al.
European Journal of Neurology|October 15, 2014
Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosisChristina Sundal, Matt Baker, Virginija Karrenbauer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutationStuart Pickering-Brown, Matt Baker, Thomas Bird, et al.
BMC Genomics|October 29, 2011
Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutationsJannet Kocerha, Naomi Kouri, Matt Baker, et al.
Pageof 9