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Anne De Septenville

Showing results (1-10 of 22) with videos related to

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BMC Bioinformatics|February 28, 2023
Reconstructing B cell lineage trees with minimum spanning tree and genotype abundancesNika Abdollahi, Lucile Jeusset, Anne de Septenville, et al.
Neurobiology of Aging|June 14, 2013
TREM2 mutations are rare in a French cohort of patients with frontotemporal dementiaSerena Lattante, Isabelle Le Ber, 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.
JAMA Neurology|October 16, 2014
Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulinPaola Caroppo, Isabelle Le Ber, Agnès Camuzat, et al.
JAMA Neurology|December 30, 2014
Posterior cortical atrophy as an extreme phenotype of GRN mutationsPaola Caroppo, Catherine Belin, David Grabli, et al.
Neurobiology of Aging|June 10, 2014
Homozygous TREM2 mutation in a family with atypical frontotemporal dementiaIsabelle Le Ber, Anne De Septenville, Rita Guerreiro, et al.
Annales De Biologie Clinique|October 7, 2020
[Watch out for a second train]Clotilde Bravetti, Magali Le Garff-Tavernier, Anne De Septenville, et al.
Neurobiology of Aging|October 15, 2013
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypesIsabelle Le Ber, Inge Van Bortel, Gael Nicolas, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, 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.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
BMC Bioinformatics|February 28, 2023
Reconstructing B cell lineage trees with minimum spanning tree and genotype abundancesNika Abdollahi, Lucile Jeusset, Anne de Septenville, et al.
Neurobiology of Aging|June 14, 2013
TREM2 mutations are rare in a French cohort of patients with frontotemporal dementiaSerena Lattante, Isabelle Le Ber, 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.
JAMA Neurology|October 16, 2014
Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulinPaola Caroppo, Isabelle Le Ber, Agnès Camuzat, et al.
JAMA Neurology|December 30, 2014
Posterior cortical atrophy as an extreme phenotype of GRN mutationsPaola Caroppo, Catherine Belin, David Grabli, et al.
Neurobiology of Aging|June 10, 2014
Homozygous TREM2 mutation in a family with atypical frontotemporal dementiaIsabelle Le Ber, Anne De Septenville, Rita Guerreiro, et al.
Annales De Biologie Clinique|October 7, 2020
[Watch out for a second train]Clotilde Bravetti, Magali Le Garff-Tavernier, Anne De Septenville, et al.
Neurobiology of Aging|October 15, 2013
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypesIsabelle Le Ber, Inge Van Bortel, Gael Nicolas, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, 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.
Pageof 3