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Matt Baker

Showing results (11-20 of 88) with videos related to

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Appetite|July 27, 2024
Nanofood insights: A survey of U.S. consumers' attitudes toward the use of nanotechnology in food processingJean A Parrella, Holli R Leggette, Peng Lu, et al.
Foods (Basel, Switzerland)|September 9, 2023
Evaluating Factors Explaining U.S. Consumers' Behavioral Intentions toward Irradiated Ground BeefJean A Parrella, Holli R Leggette, Peng Lu, et al.
Alzheimer Disease and Associated Disorders|June 10, 2003
Familial primary progressive aphasiaThomas A Krefft, Neill R Graff-Radford, Dennis W Dickson, et al.
Brain : a Journal of Neurology|August 14, 2009
A new subtype of frontotemporal lobar degeneration with FUS pathologyManuela Neumann, Rosa Rademakers, Sigrun Roeber, et al.
Acta Neuropathologica|August 12, 2009
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion diseaseManuela Neumann, Sigrun Roeber, Hans A Kretzschmar, et al.
Angewandte Chemie (International Ed. in English)|March 25, 2025
Cl<sub>3</sub>Al-PH<sub>3</sub> Is a Weak Lewis Pair Allowing the Synthesis of Sterically Highly Hindered Primary and Secondary Alkyl PhosphanesHansjörg Grützmacher, Jan Oswald, Csilla Fekete, et al.
Annals of Neurology|June 14, 2008
Gene expression study on peripheral blood identifies progranulin mutationsGiovanni Coppola, Anna Karydas, Rosa Rademakers, et al.
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|October 1, 2013
Psychosis and hallucinations in frontotemporal dementia with the C9ORF72 mutation: a detailed clinical cohortAndrew Kertesz, Lee Cyn Ang, Sarah Jesso, et al.
Journal of Neuropathology and Experimental Neurology|June 20, 2019
Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1Shunsuke Koga, J Eric Ahlskog, Michael A DeTure, et al.
American Journal of Neurodegenerative Disease|February 6, 2013
C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo ClinicAleksandra Wojtas, Kristin A Heggeli, Nicole Finch, et al.
Pageof 9

Showing results (11-20 of 88) with videos related to

Sort By:
Pageof 9
Appetite|July 27, 2024
Nanofood insights: A survey of U.S. consumers' attitudes toward the use of nanotechnology in food processingJean A Parrella, Holli R Leggette, Peng Lu, et al.
Foods (Basel, Switzerland)|September 9, 2023
Evaluating Factors Explaining U.S. Consumers' Behavioral Intentions toward Irradiated Ground BeefJean A Parrella, Holli R Leggette, Peng Lu, et al.
Alzheimer Disease and Associated Disorders|June 10, 2003
Familial primary progressive aphasiaThomas A Krefft, Neill R Graff-Radford, Dennis W Dickson, et al.
Brain : a Journal of Neurology|August 14, 2009
A new subtype of frontotemporal lobar degeneration with FUS pathologyManuela Neumann, Rosa Rademakers, Sigrun Roeber, et al.
Acta Neuropathologica|August 12, 2009
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion diseaseManuela Neumann, Sigrun Roeber, Hans A Kretzschmar, et al.
Angewandte Chemie (International Ed. in English)|March 25, 2025
Cl<sub>3</sub>Al-PH<sub>3</sub> Is a Weak Lewis Pair Allowing the Synthesis of Sterically Highly Hindered Primary and Secondary Alkyl PhosphanesHansjörg Grützmacher, Jan Oswald, Csilla Fekete, et al.
Annals of Neurology|June 14, 2008
Gene expression study on peripheral blood identifies progranulin mutationsGiovanni Coppola, Anna Karydas, Rosa Rademakers, et al.
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|October 1, 2013
Psychosis and hallucinations in frontotemporal dementia with the C9ORF72 mutation: a detailed clinical cohortAndrew Kertesz, Lee Cyn Ang, Sarah Jesso, et al.
Journal of Neuropathology and Experimental Neurology|June 20, 2019
Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1Shunsuke Koga, J Eric Ahlskog, Michael A DeTure, et al.
American Journal of Neurodegenerative Disease|February 6, 2013
C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo ClinicAleksandra Wojtas, Kristin A Heggeli, Nicole Finch, et al.
Pageof 9