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Isabelle Le Ber

Showing results (51-60 of 211) with videos related to

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Scientific Reports|May 12, 2017
Pathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substratesFernando Bartolome, Noemi Esteras, Angeles Martin-Requero, et al.
Neurology. Genetics|December 22, 2017
Factors influencing the age at onset in familial frontotemporal lobar dementia: Important weight of geneticsMathieu Barbier, Agnès Camuzat, Marion Houot, et al.
Journal of Alzheimer'S Disease : JAD|June 16, 2012
Clinical, neuropathological, and biochemical characterization of the novel tau mutation P332SVincent Deramecourt, Florence Lebert, Claude-Alain Maurage, et al.
American Journal of Human Genetics|October 13, 2015
A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar AtaxiaMarie Coutelier, Iulia Blesneac, Arnaud Monteil, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 5, 2011
Fronto-temporal lobar degeneration: neuropathology in 60 casesDanielle Seilhean, Isabelle Le Ber, Marie Sarazin, et al.
Brain : a Journal of Neurology|January 23, 2004
Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patientsIsabelle Le Ber, Naïma Bouslam, Sophie Rivaud-Péchoux, et al.
JAMA Neurology|December 18, 2013
DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypesPaola Caroppo, Isabelle Le Ber, Fabienne Clot, et al.
Neurobiology of Aging|July 3, 2019
The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiencyDario Saracino, Leila Sellami, Fabienne Clot, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 10, 2025
Quantifying multimodal longitudinal brain changes in presymptomatic C9orf72 diseaseDario Saracino, Lorenzo Cipriano, Marion Houot, et al.
Journal of Alzheimer'S Disease : JAD|December 16, 2010
FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosisOriane Broustal, Agnès Camuzat, Lena Guillot-Noël, et al.
Pageof 22

Showing results (51-60 of 211) with videos related to

Sort By:
Pageof 22
Scientific Reports|May 12, 2017
Pathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substratesFernando Bartolome, Noemi Esteras, Angeles Martin-Requero, et al.
Neurology. Genetics|December 22, 2017
Factors influencing the age at onset in familial frontotemporal lobar dementia: Important weight of geneticsMathieu Barbier, Agnès Camuzat, Marion Houot, et al.
Journal of Alzheimer'S Disease : JAD|June 16, 2012
Clinical, neuropathological, and biochemical characterization of the novel tau mutation P332SVincent Deramecourt, Florence Lebert, Claude-Alain Maurage, et al.
American Journal of Human Genetics|October 13, 2015
A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar AtaxiaMarie Coutelier, Iulia Blesneac, Arnaud Monteil, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 5, 2011
Fronto-temporal lobar degeneration: neuropathology in 60 casesDanielle Seilhean, Isabelle Le Ber, Marie Sarazin, et al.
Brain : a Journal of Neurology|January 23, 2004
Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patientsIsabelle Le Ber, Naïma Bouslam, Sophie Rivaud-Péchoux, et al.
JAMA Neurology|December 18, 2013
DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypesPaola Caroppo, Isabelle Le Ber, Fabienne Clot, et al.
Neurobiology of Aging|July 3, 2019
The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiencyDario Saracino, Leila Sellami, Fabienne Clot, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 10, 2025
Quantifying multimodal longitudinal brain changes in presymptomatic C9orf72 diseaseDario Saracino, Lorenzo Cipriano, Marion Houot, et al.
Journal of Alzheimer'S Disease : JAD|December 16, 2010
FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosisOriane Broustal, Agnès Camuzat, Lena Guillot-Noël, et al.
Pageof 22