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Emily Todd

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Clinical Genetics|July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorderStephanie Oates, Michael Absoud, Sushma Goyal, et al.
Journal of Alzheimer'S Disease : JAD|January 24, 2022
An Automated Toolbox to Predict Single Subject Atrophy in Presymptomatic Granulin Mutation CarriersEnrico Premi, Tommaso Costa, Stefano Gazzina, et al.
Journal of Neurology|March 29, 2022
Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutationsArabella Bouzigues, Lucy L Russell, Georgia Peakman, et al.
Neurology|June 23, 2021
Characterizing the Clinical Features and Atrophy Patterns of <i>MAPT</i>-Related Frontotemporal Dementia With Disease Progression ModelingAlexandra L Young, Martina Bocchetta, Lucy L Russell, et al.
JAMA Network Open|January 6, 2021
Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal DementiaAlberto Benussi, Enrico Premi, Stefano Gazzina, et al.
Neurobiology of Aging|October 4, 2021
Dissemination in time and space in presymptomatic granulin mutation carriers: a GENFI spatial chronnectome studyEnrico Premi, Marcello Giunta, Armin Iraji, et al.
Neurobiology of Aging|September 5, 2022
Corrigendum to "Dissemination in time and space in presymptomatic granulin mutation carriers: A spatial chronnectome study" [Neurobiology of Aging Volume 108, December 2021, Pages 155-167]Enrico Premi, Marcello Giunta, Armin Iraji, et al.
Journal of Neuroinflammation|September 5, 2022
Elevated CSF and plasma complement proteins in genetic frontotemporal dementia: results from the GENFI studyEmma L van der Ende, Carolin Heller, Aitana Sogorb-Esteve, et al.
American Journal of Human Genetics|January 5, 2024
Building a vertically integrated genomic learning health system: The biobank at the Colorado Center for Personalized MedicineLaura K Wiley, Jonathan A Shortt, Emily R Roberts, et al.
Neurology|April 8, 2021
Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar DegenerationJulio C Rojas, Ping Wang, Adam M Staffaroni, et al.
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Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Clinical Genetics|July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorderStephanie Oates, Michael Absoud, Sushma Goyal, et al.
Journal of Alzheimer'S Disease : JAD|January 24, 2022
An Automated Toolbox to Predict Single Subject Atrophy in Presymptomatic Granulin Mutation CarriersEnrico Premi, Tommaso Costa, Stefano Gazzina, et al.
Journal of Neurology|March 29, 2022
Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutationsArabella Bouzigues, Lucy L Russell, Georgia Peakman, et al.
Neurology|June 23, 2021
Characterizing the Clinical Features and Atrophy Patterns of <i>MAPT</i>-Related Frontotemporal Dementia With Disease Progression ModelingAlexandra L Young, Martina Bocchetta, Lucy L Russell, et al.
JAMA Network Open|January 6, 2021
Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal DementiaAlberto Benussi, Enrico Premi, Stefano Gazzina, et al.
Neurobiology of Aging|October 4, 2021
Dissemination in time and space in presymptomatic granulin mutation carriers: a GENFI spatial chronnectome studyEnrico Premi, Marcello Giunta, Armin Iraji, et al.
Neurobiology of Aging|September 5, 2022
Corrigendum to "Dissemination in time and space in presymptomatic granulin mutation carriers: A spatial chronnectome study" [Neurobiology of Aging Volume 108, December 2021, Pages 155-167]Enrico Premi, Marcello Giunta, Armin Iraji, et al.
Journal of Neuroinflammation|September 5, 2022
Elevated CSF and plasma complement proteins in genetic frontotemporal dementia: results from the GENFI studyEmma L van der Ende, Carolin Heller, Aitana Sogorb-Esteve, et al.
American Journal of Human Genetics|January 5, 2024
Building a vertically integrated genomic learning health system: The biobank at the Colorado Center for Personalized MedicineLaura K Wiley, Jonathan A Shortt, Emily R Roberts, et al.
Neurology|April 8, 2021
Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar DegenerationJulio C Rojas, Ping Wang, Adam M Staffaroni, et al.
Pageof 3