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Showing results (971-980 of 1,083) with videos related to

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JAMA Neurology|January 30, 2023
Incidence of Syndromes Associated With Frontotemporal Lobar Degeneration in 9 European CountriesGiancarlo Logroscino, Marco Piccininni, Caroline Graff, et al.
Neurology. Genetics|July 24, 2025
Executive Function Deficits in Genetic Frontotemporal Dementia: Results From the GENFI StudyLucy Louise Russell, Arabella Bouzigues, Rhian S Convery, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2026
Biomarkers of Leucine-Rich Repeat Kinase 2 (LRRK2) and Lysosomal Dysfunction in Progressive Supranuclear PalsyLouise-Kristine Nielsen, Joshua L I Frost, David P Vaughan, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|November 22, 2020
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohortLucy L Russell, Caroline V Greaves, Martina Bocchetta, et al.
Annals of Clinical and Translational Neurology|August 11, 2022
The CBI-R detects early behavioural impairment in genetic frontotemporal dementiaAnnabel Nelson, Lucy L Russell, Georgia Peakman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersMaurice Pasternak, Saira S Mirza, Andrew D Paterson, et al.
Brain : a Journal of Neurology|February 21, 2022
Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementiaGolia Shafiei, Vincent Bazinet, Mahsa Dadar, et al.
Annals of Clinical and Translational Neurology|August 11, 2020
Neuronal intranuclear inclusion disease is genetically heterogeneousZhongbo Chen, Wai Yan Yau, Zane Jaunmuktane, et al.
Brain Communications|November 19, 2020
Analysis of brain atrophy and local gene expression in genetic frontotemporal dementiaAndre Altmann, David M Cash, Martina Bocchetta, et al.
Molecular Psychiatry|October 4, 2018
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral seriesC Koriath, J Kenny, G Adamson, et al.
Pageof 109

Showing results (971-980 of 1,083) with videos related to

Sort By:
Pageof 109
JAMA Neurology|January 30, 2023
Incidence of Syndromes Associated With Frontotemporal Lobar Degeneration in 9 European CountriesGiancarlo Logroscino, Marco Piccininni, Caroline Graff, et al.
Neurology. Genetics|July 24, 2025
Executive Function Deficits in Genetic Frontotemporal Dementia: Results From the GENFI StudyLucy Louise Russell, Arabella Bouzigues, Rhian S Convery, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 16, 2026
Biomarkers of Leucine-Rich Repeat Kinase 2 (LRRK2) and Lysosomal Dysfunction in Progressive Supranuclear PalsyLouise-Kristine Nielsen, Joshua L I Frost, David P Vaughan, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|November 22, 2020
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohortLucy L Russell, Caroline V Greaves, Martina Bocchetta, et al.
Annals of Clinical and Translational Neurology|August 11, 2022
The CBI-R detects early behavioural impairment in genetic frontotemporal dementiaAnnabel Nelson, Lucy L Russell, Georgia Peakman, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
BiomarkersMaurice Pasternak, Saira S Mirza, Andrew D Paterson, et al.
Brain : a Journal of Neurology|February 21, 2022
Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementiaGolia Shafiei, Vincent Bazinet, Mahsa Dadar, et al.
Annals of Clinical and Translational Neurology|August 11, 2020
Neuronal intranuclear inclusion disease is genetically heterogeneousZhongbo Chen, Wai Yan Yau, Zane Jaunmuktane, et al.
Brain Communications|November 19, 2020
Analysis of brain atrophy and local gene expression in genetic frontotemporal dementiaAndre Altmann, David M Cash, Martina Bocchetta, et al.
Molecular Psychiatry|October 4, 2018
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral seriesC Koriath, J Kenny, G Adamson, et al.
Pageof 109