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Isabelle Le Ber

Showing results (101-110 of 211) with videos related to

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Journal of Alzheimer'S Disease : JAD|May 11, 2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 MutationsElkin Luis, Alexandra Ortiz, Luis Eudave, et al.
Neurology|July 29, 2016
Seizures in dominantly inherited Alzheimer diseaseAline Zarea, Camille Charbonnier, Anne Rovelet-Lecrux, et al.
Frontiers in Cellular Neuroscience|May 4, 2023
C9ORF72 knockdown triggers FTD-like symptoms and cell pathology in miceMaria-Belen Lopez-Herdoiza, Stephanie Bauché, Baptiste Wilmet, et al.
Journal of Neurology|June 28, 2020
High diagnostic value of plasma Niemann-Pick type C biomarkers in adults with selected neurological and/or psychiatric disordersDaniele Mandia, Marion Plaze, Isabelle Le Ber, et al.
Brain : a Journal of Neurology|December 20, 2021
Motor neuron pathology in CANVAS due to RFC1 expansionsVincent Huin, Giulia Coarelli, Clément Guemy, et al.
Journal of Alzheimer'S Disease : JAD|September 25, 2015
Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?Paola Caroppo, Marie-Odile Habert, Stanley Durrleman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2021
Plasma NfL levels and longitudinal change rates in <i>C9orf72</i> and <i>GRN</i>-associated diseases: from tailored references to clinical applicationsDario Saracino, Karim Dorgham, Agnès Camuzat, et al.
Human Mutation|April 17, 2007
Progranulin null mutations in both sporadic and familial frontotemporal dementiaIsabelle Le Ber, Julie van der Zee, Didier Hannequin, et al.
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.
Pageof 22

Showing results (101-110 of 211) with videos related to

Sort By:
Pageof 22
Journal of Alzheimer'S Disease : JAD|May 11, 2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 MutationsElkin Luis, Alexandra Ortiz, Luis Eudave, et al.
Neurology|July 29, 2016
Seizures in dominantly inherited Alzheimer diseaseAline Zarea, Camille Charbonnier, Anne Rovelet-Lecrux, et al.
Frontiers in Cellular Neuroscience|May 4, 2023
C9ORF72 knockdown triggers FTD-like symptoms and cell pathology in miceMaria-Belen Lopez-Herdoiza, Stephanie Bauché, Baptiste Wilmet, et al.
Journal of Neurology|June 28, 2020
High diagnostic value of plasma Niemann-Pick type C biomarkers in adults with selected neurological and/or psychiatric disordersDaniele Mandia, Marion Plaze, Isabelle Le Ber, et al.
Brain : a Journal of Neurology|December 20, 2021
Motor neuron pathology in CANVAS due to RFC1 expansionsVincent Huin, Giulia Coarelli, Clément Guemy, et al.
Journal of Alzheimer'S Disease : JAD|September 25, 2015
Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?Paola Caroppo, Marie-Odile Habert, Stanley Durrleman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 5, 2021
Plasma NfL levels and longitudinal change rates in <i>C9orf72</i> and <i>GRN</i>-associated diseases: from tailored references to clinical applicationsDario Saracino, Karim Dorgham, Agnès Camuzat, et al.
Human Mutation|April 17, 2007
Progranulin null mutations in both sporadic and familial frontotemporal dementiaIsabelle Le Ber, Julie van der Zee, Didier Hannequin, et al.
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.
Pageof 22