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Isabelle Le

Showing results (361-370 of 473) with videos related to

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Acta Neuropathologica|June 7, 2021
Clinical and neuropathological diversity of tauopathy in MAPT duplication carriersDavid Wallon, Susana Boluda, Anne Rovelet-Lecrux, et al.
JAMA Neurology|May 8, 2013
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R geneRita Guerreiro, Eleanna Kara, Isabelle Le Ber, et al.
Brain : a Journal of Neurology|June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Journal of Medical Genetics|June 26, 2010
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlationsStéphanie Millecamps, François Salachas, Cécile Cazeneuve, et al.
Nature Communications|June 4, 2015
Microtubule-associated protein 6 mediates neuronal connectivity through Semaphorin 3E-dependent signalling for axonal growthJean-Christophe Deloulme, Sylvie Gory-Fauré, Franck Mauconduit, et al.
Brain Communications|June 30, 2025
Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of <i>HTT</i> associated with an early disease onset in <i>C9orf72</i> carriersMathieu Barbier, Thomas Gareau, Agnès Camuzat, et al.
Blood|February 7, 2025
Targeting cell-surface VISTA expression on allospecific naïve T cells promotes toleranceBrent H Koehn, Elizabeth C Nowak, Sladjana Skopelja-Gardner, et al.
Human Mutation|March 9, 2007
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementiaJulie van der Zee, Isabelle Le Ber, Sebastian Maurer-Stroh, et al.
Brain : a Journal of Neurology|October 31, 2006
Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementiaIsabelle Le Ber, Eric Guedj, Audrey Gabelle, et al.
Neurobiology of Disease|April 1, 2023
Plasma lysosphingolipids in GRN-related diseases: Monitoring lysosomal dysfunction to track disease progressionWalid Khrouf, Dario Saracino, Benoit Rucheton, et al.
Pageof 48

Showing results (361-370 of 473) with videos related to

Sort By:
Pageof 48
Acta Neuropathologica|June 7, 2021
Clinical and neuropathological diversity of tauopathy in MAPT duplication carriersDavid Wallon, Susana Boluda, Anne Rovelet-Lecrux, et al.
JAMA Neurology|May 8, 2013
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R geneRita Guerreiro, Eleanna Kara, Isabelle Le Ber, et al.
Brain : a Journal of Neurology|June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Journal of Medical Genetics|June 26, 2010
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlationsStéphanie Millecamps, François Salachas, Cécile Cazeneuve, et al.
Nature Communications|June 4, 2015
Microtubule-associated protein 6 mediates neuronal connectivity through Semaphorin 3E-dependent signalling for axonal growthJean-Christophe Deloulme, Sylvie Gory-Fauré, Franck Mauconduit, et al.
Brain Communications|June 30, 2025
Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of <i>HTT</i> associated with an early disease onset in <i>C9orf72</i> carriersMathieu Barbier, Thomas Gareau, Agnès Camuzat, et al.
Blood|February 7, 2025
Targeting cell-surface VISTA expression on allospecific naïve T cells promotes toleranceBrent H Koehn, Elizabeth C Nowak, Sladjana Skopelja-Gardner, et al.
Human Mutation|March 9, 2007
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementiaJulie van der Zee, Isabelle Le Ber, Sebastian Maurer-Stroh, et al.
Brain : a Journal of Neurology|October 31, 2006
Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementiaIsabelle Le Ber, Eric Guedj, Audrey Gabelle, et al.
Neurobiology of Disease|April 1, 2023
Plasma lysosphingolipids in GRN-related diseases: Monitoring lysosomal dysfunction to track disease progressionWalid Khrouf, Dario Saracino, Benoit Rucheton, et al.
Pageof 48