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 (1-10 of 211) with videos related to

Pageof 22
Sort By:
Presse Medicale (Paris, France : 1983)|June 9, 2007
[Frontotemporal dementia]Isabelle Le Ber, Bruno Dubois
Advances in Experimental Medicine and Biology|January 12, 2021
Clinical Update on C9orf72: Frontotemporal Dementia, Amyotrophic Lateral Sclerosis, and BeyondDario Saracino, Isabelle Le Ber
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|September 1, 2018
Monogenic inheritance in early-onset dementia: illustration in Alzheimer's disease and frontotemporal lobar dementiaMathieu Barbier, David Wallon, Isabelle Le Ber
Current Neurology and Neuroscience Reports|September 1, 2005
New autosomal recessive cerebellar ataxias with oculomotor apraxiaIsabelle Le Ber, Alexis Brice, Alexandra Dürr
Neurobiology of Aging|November 28, 2012
Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in FranceSerena Lattante, Isabelle Le Ber, Agnès Camuzat, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|September 6, 2017
Structural magnetic resonance imaging in frontotemporal lobar dementiaAnne Bertrand, Sebastian Stroër, Isabelle Le Ber, et al.
Neurobiology of Aging|April 16, 2013
Screening UBQLN-2 in French frontotemporal lobar degeneration and frontotemporal lobar degeneration-amyotrophic lateral sclerosis patientsSerena Lattante, Isabelle Le Ber, Agnès Camuzat, et al.
Journal of the Neurological Sciences|May 8, 2007
Neuropsychological and 18FDG-PET studies in a family with idiopathic basal ganglia calcificationsIsabelle Le Ber, Rose-Marie Marié, Benoît Chabot, et al.
Human Molecular Genetics|November 21, 2014
Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLDSerena Lattante, Hortense de Calbiac, Isabelle Le Ber, et al.
Annals of Neurology|May 31, 2013
Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosisSorana Ciura, Serena Lattante, Isabelle Le Ber, et al.
Pageof 22

Showing results (1-10 of 211) with videos related to

Sort By:
Pageof 22
Presse Medicale (Paris, France : 1983)|June 9, 2007
[Frontotemporal dementia]Isabelle Le Ber, Bruno Dubois
Advances in Experimental Medicine and Biology|January 12, 2021
Clinical Update on C9orf72: Frontotemporal Dementia, Amyotrophic Lateral Sclerosis, and BeyondDario Saracino, Isabelle Le Ber
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|September 1, 2018
Monogenic inheritance in early-onset dementia: illustration in Alzheimer's disease and frontotemporal lobar dementiaMathieu Barbier, David Wallon, Isabelle Le Ber
Current Neurology and Neuroscience Reports|September 1, 2005
New autosomal recessive cerebellar ataxias with oculomotor apraxiaIsabelle Le Ber, Alexis Brice, Alexandra Dürr
Neurobiology of Aging|November 28, 2012
Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in FranceSerena Lattante, Isabelle Le Ber, Agnès Camuzat, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|September 6, 2017
Structural magnetic resonance imaging in frontotemporal lobar dementiaAnne Bertrand, Sebastian Stroër, Isabelle Le Ber, et al.
Neurobiology of Aging|April 16, 2013
Screening UBQLN-2 in French frontotemporal lobar degeneration and frontotemporal lobar degeneration-amyotrophic lateral sclerosis patientsSerena Lattante, Isabelle Le Ber, Agnès Camuzat, et al.
Journal of the Neurological Sciences|May 8, 2007
Neuropsychological and 18FDG-PET studies in a family with idiopathic basal ganglia calcificationsIsabelle Le Ber, Rose-Marie Marié, Benoît Chabot, et al.
Human Molecular Genetics|November 21, 2014
Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLDSerena Lattante, Hortense de Calbiac, Isabelle Le Ber, et al.
Annals of Neurology|May 31, 2013
Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosisSorana Ciura, Serena Lattante, Isabelle Le Ber, et al.
Pageof 22