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Isabelle Le Ber

Showing results (131-140 of 211) with videos related to

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Journal of Alzheimer'S Disease : JAD|December 21, 2012
C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testingIsabelle Le Ber, Agnès Camuzat, Lena Guillot-Noel, et al.
Neurology|November 11, 2024
Association of Changes in Cerebral and Hypothalamic Structure With Sleep Dysfunction in Patients With Genetic Frontotemporal DementiaP Tristin Best, John C Van Swieten, Lize Corrine Jiskoot, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|April 16, 2024
Extending the phenotypic spectrum assessed by the CDR plus NACC FTLD in genetic frontotemporal dementiaKiran Samra, Georgia Peakman, Amy M MacDougall, et al.
Brain : a Journal of Neurology|December 15, 2007
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degenerationGiovanni Stevanin, Hamid Azzedine, Paola Denora, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 17, 2024
Frontoparietal network integrity supports cognitive function in pre-symptomatic frontotemporal dementia: Multimodal analysis of brain function, structure, and perfusionXulin Liu, Peter Simon Jones, Maurice Pasternak, et al.
Neurology|September 4, 2025
Cerebrovascular Reactivity at Rest and Its Association With Cognitive Function in People With Genetic Frontotemporal DementiaIvana Kirilova Kancheva, Arabella Bouzigues, Lucy Louise Russell, et al.
Alzheimer'S Research & Therapy|July 13, 2021
The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohortHannah D Franklin, Lucy L Russell, Georgia Peakman, et al.
Plos Medicine|March 29, 2017
APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic casesHélène-Marie Lanoiselée, Gaël Nicolas, David Wallon, et al.
Neurology|May 13, 2021
Primary Progressive Aphasia Associated With <i>GRN</i> Mutations: New Insights Into the Nonamyloid Logopenic VariantDario Saracino, Sophie Ferrieux, Marie Noguès-Lassiaille, et al.
Journal of Neurology|December 20, 2022
Language impairment in the genetic forms of behavioural variant frontotemporal dementiaKiran Samra, Amy M MacDougall, Arabella Bouzigues, et al.
Pageof 22

Showing results (131-140 of 211) with videos related to

Sort By:
Pageof 22
Journal of Alzheimer'S Disease : JAD|December 21, 2012
C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testingIsabelle Le Ber, Agnès Camuzat, Lena Guillot-Noel, et al.
Neurology|November 11, 2024
Association of Changes in Cerebral and Hypothalamic Structure With Sleep Dysfunction in Patients With Genetic Frontotemporal DementiaP Tristin Best, John C Van Swieten, Lize Corrine Jiskoot, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|April 16, 2024
Extending the phenotypic spectrum assessed by the CDR plus NACC FTLD in genetic frontotemporal dementiaKiran Samra, Georgia Peakman, Amy M MacDougall, et al.
Brain : a Journal of Neurology|December 15, 2007
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degenerationGiovanni Stevanin, Hamid Azzedine, Paola Denora, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 17, 2024
Frontoparietal network integrity supports cognitive function in pre-symptomatic frontotemporal dementia: Multimodal analysis of brain function, structure, and perfusionXulin Liu, Peter Simon Jones, Maurice Pasternak, et al.
Neurology|September 4, 2025
Cerebrovascular Reactivity at Rest and Its Association With Cognitive Function in People With Genetic Frontotemporal DementiaIvana Kirilova Kancheva, Arabella Bouzigues, Lucy Louise Russell, et al.
Alzheimer'S Research & Therapy|July 13, 2021
The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohortHannah D Franklin, Lucy L Russell, Georgia Peakman, et al.
Plos Medicine|March 29, 2017
APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic casesHélène-Marie Lanoiselée, Gaël Nicolas, David Wallon, et al.
Neurology|May 13, 2021
Primary Progressive Aphasia Associated With <i>GRN</i> Mutations: New Insights Into the Nonamyloid Logopenic VariantDario Saracino, Sophie Ferrieux, Marie Noguès-Lassiaille, et al.
Journal of Neurology|December 20, 2022
Language impairment in the genetic forms of behavioural variant frontotemporal dementiaKiran Samra, Amy M MacDougall, Arabella Bouzigues, et al.
Pageof 22