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Isabelle Le Ber

Showing results (31-40 of 211) with videos related to

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Archives of Neurology|August 20, 2003
Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxiaIsabelle Le Ber, Agnès Camuzat, Giovanni Castelnovo, et al.
Archives of Neurology|June 16, 2005
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophyValérie Biancalana, Mathias Toft, Isabelle Le Ber, et al.
Frontiers in Neuroscience|September 14, 2018
New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion CarriersArthur Viodé, Clémence Fournier, Agnès Camuzat, et al.
Neurobiology of Aging|August 28, 2014
Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patientsStéphanie Millecamps, Anne De Septenville, Elisa Teyssou, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|January 19, 2023
Behavioural disinhibition in frontotemporal dementia investigated within an ecological frameworkDelphine Tanguy, Armelle Rametti-Lacroux, Arabella Bouzigues, et al.
Neurobiology of Aging|August 3, 2014
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansionsSerena Lattante, Isabelle Le Ber, Daniela Galimberti, et al.
Acta Neuropathologica|May 31, 2019
Increased prevalence of granulovacuolar degeneration in C9orf72 mutationYuichi Riku, Charles Duyckaerts, Susana Boluda, et al.
Neurobiology of Aging|November 6, 2016
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlationsCinzia Coppola, Dario Saracino, Gianfranco Puoti, et al.
Neurobiology of Disease|May 16, 2008
Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson diseaseAnne Rovelet-Lecrux, Vincent Deramecourt, Solenn Legallic, et al.
JAMA Neurology|December 30, 2014
Posterior cortical atrophy as an extreme phenotype of GRN mutationsPaola Caroppo, Catherine Belin, David Grabli, et al.
Pageof 22

Showing results (31-40 of 211) with videos related to

Sort By:
Pageof 22
Archives of Neurology|August 20, 2003
Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxiaIsabelle Le Ber, Agnès Camuzat, Giovanni Castelnovo, et al.
Archives of Neurology|June 16, 2005
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophyValérie Biancalana, Mathias Toft, Isabelle Le Ber, et al.
Frontiers in Neuroscience|September 14, 2018
New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion CarriersArthur Viodé, Clémence Fournier, Agnès Camuzat, et al.
Neurobiology of Aging|August 28, 2014
Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patientsStéphanie Millecamps, Anne De Septenville, Elisa Teyssou, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|January 19, 2023
Behavioural disinhibition in frontotemporal dementia investigated within an ecological frameworkDelphine Tanguy, Armelle Rametti-Lacroux, Arabella Bouzigues, et al.
Neurobiology of Aging|August 3, 2014
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansionsSerena Lattante, Isabelle Le Ber, Daniela Galimberti, et al.
Acta Neuropathologica|May 31, 2019
Increased prevalence of granulovacuolar degeneration in C9orf72 mutationYuichi Riku, Charles Duyckaerts, Susana Boluda, et al.
Neurobiology of Aging|November 6, 2016
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlationsCinzia Coppola, Dario Saracino, Gianfranco Puoti, et al.
Neurobiology of Disease|May 16, 2008
Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson diseaseAnne Rovelet-Lecrux, Vincent Deramecourt, Solenn Legallic, et al.
JAMA Neurology|December 30, 2014
Posterior cortical atrophy as an extreme phenotype of GRN mutationsPaola Caroppo, Catherine Belin, David Grabli, et al.
Pageof 22