Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Isabelle Le Ber

Showing results (61-70 of 211) with videos related to

Pageof 22
Sort By:
Journal of Alzheimer'S Disease : JAD|August 13, 2014
A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutationClaire Boutoleau-Bretonnière, Agnès Camuzat, Isabelle Le Ber, et al.
Brain : a Journal of Neurology|September 25, 2003
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studiesIsabelle Le Ber, Maria-Ceù Moreira, Sophie Rivaud-Péchoux, et al.
Behavioral and Brain Functions : BBF|August 23, 2025
Behavioral variant frontotemporal dementia as a model for understanding the cognitive and cerebral determinants of verbal creativityVictor Altmayer, Marcela Ovando-Tellez, Théophile Bieth, et al.
Neurobiology of Aging|October 18, 2015
TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohortsIsabelle Le Ber, Anne De Septenville, Stéphanie Millecamps, et al.
Neurogenetics|January 29, 2014
Partial deletions of the GRN gene are a cause of frontotemporal lobar degenerationFabienne Clot, Anne Rovelet-Lecrux, Foudil Lamari, et al.
Alzheimer'S Research & Therapy|January 9, 2021
Characteristics and progression of patients with frontotemporal dementia in a regional memory clinic networkMélanie Leroy, Maxime Bertoux, Emilie Skrobala, et al.
Brain : a Journal of Neurology|June 25, 2004
A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24Isabelle Le Ber, Maria Martinez, Dominique Campion, et al.
Neuroimage. Clinical|June 14, 2022
An ecological approach to identify distinct neural correlates of disinhibition in frontotemporal dementiaDelphine Tanguy, Bénédicte Batrancourt, Alfonso Estudillo-Romero, et al.
Journal of Alzheimer'S Disease : JAD|October 5, 2020
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman EmpireCinzia Coppola, Dario Saracino, Mariano Oliva, et al.
Annals of Neurology|June 10, 2019
Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging studyGiorgia Querin, Peter Bede, Mohamed Mounir El Mendili, et al.
Pageof 22

Showing results (61-70 of 211) with videos related to

Sort By:
Pageof 22
Journal of Alzheimer'S Disease : JAD|August 13, 2014
A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutationClaire Boutoleau-Bretonnière, Agnès Camuzat, Isabelle Le Ber, et al.
Brain : a Journal of Neurology|September 25, 2003
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studiesIsabelle Le Ber, Maria-Ceù Moreira, Sophie Rivaud-Péchoux, et al.
Behavioral and Brain Functions : BBF|August 23, 2025
Behavioral variant frontotemporal dementia as a model for understanding the cognitive and cerebral determinants of verbal creativityVictor Altmayer, Marcela Ovando-Tellez, Théophile Bieth, et al.
Neurobiology of Aging|October 18, 2015
TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohortsIsabelle Le Ber, Anne De Septenville, Stéphanie Millecamps, et al.
Neurogenetics|January 29, 2014
Partial deletions of the GRN gene are a cause of frontotemporal lobar degenerationFabienne Clot, Anne Rovelet-Lecrux, Foudil Lamari, et al.
Alzheimer'S Research & Therapy|January 9, 2021
Characteristics and progression of patients with frontotemporal dementia in a regional memory clinic networkMélanie Leroy, Maxime Bertoux, Emilie Skrobala, et al.
Brain : a Journal of Neurology|June 25, 2004
A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24Isabelle Le Ber, Maria Martinez, Dominique Campion, et al.
Neuroimage. Clinical|June 14, 2022
An ecological approach to identify distinct neural correlates of disinhibition in frontotemporal dementiaDelphine Tanguy, Bénédicte Batrancourt, Alfonso Estudillo-Romero, et al.
Journal of Alzheimer'S Disease : JAD|October 5, 2020
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman EmpireCinzia Coppola, Dario Saracino, Mariano Oliva, et al.
Annals of Neurology|June 10, 2019
Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging studyGiorgia Querin, Peter Bede, Mohamed Mounir El Mendili, et al.
Pageof 22