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July 27, 2024
Nanofood insights: A survey of U.S. consumers' attitudes toward the use of nanotechnology in food processing
Jean 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 Beef
Jean A Parrella, Holli R Leggette, Peng Lu, et al.
Alzheimer Disease and Associated Disorders
|
June 10, 2003
Familial primary progressive aphasia
Thomas 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 pathology
Manuela Neumann, Rosa Rademakers, Sigrun Roeber, et al.
Acta Neuropathologica
|
August 12, 2009
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
Manuela 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 Phosphanes
Hansjörg Grützmacher, Jan Oswald, Csilla Fekete, et al.
Annals of Neurology
|
June 14, 2008
Gene expression study on peripheral blood identifies progranulin mutations
Giovanni 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 cohort
Andrew 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 1
Shunsuke 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 Clinic
Aleksandra Wojtas, Kristin A Heggeli, Nicole Finch, et al.
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Search research articles
Search
Showing results (11-20 of 88) with videos related to
Sort By:
Page
of 9
Appetite
|
July 27, 2024
Nanofood insights: A survey of U.S. consumers' attitudes toward the use of nanotechnology in food processing
Jean 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 Beef
Jean A Parrella, Holli R Leggette, Peng Lu, et al.
Alzheimer Disease and Associated Disorders
|
June 10, 2003
Familial primary progressive aphasia
Thomas 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 pathology
Manuela Neumann, Rosa Rademakers, Sigrun Roeber, et al.
Acta Neuropathologica
|
August 12, 2009
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease
Manuela 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 Phosphanes
Hansjörg Grützmacher, Jan Oswald, Csilla Fekete, et al.
Annals of Neurology
|
June 14, 2008
Gene expression study on peripheral blood identifies progranulin mutations
Giovanni 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 cohort
Andrew 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 1
Shunsuke 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 Clinic
Aleksandra Wojtas, Kristin A Heggeli, Nicole Finch, et al.
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of 9