Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Isabelle Le

Showing results (371-380 of 473) with videos related to

Pageof 48
Sort By:
Brain : a Journal of Neurology|November 15, 2025
The genetic landscape of frontotemporal lobar degeneration: investigation of a diagnostic cohort of 2747 probandsGuillaume Cogan, Marion Houot, Julie Bogoin, et al.
BMC Research Notes|October 2, 2023
RNAseq based variant dataset in a black poplar association panelOdile Rogier, Aurélien Chateigner, Marie-Claude Lesage-Descauses, et al.
Brain : a Journal of Neurology|November 17, 2021
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxiaMarie Coutelier, Maxime Jacoupy, Alexandre Janer, et al.
Journal of Alzheimer'S Disease : JAD|April 6, 2012
The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkersDavid Wallon, Stéphane Rousseau, Anne Rovelet-Lecrux, et al.
Brain : a Journal of Neurology|February 5, 2008
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic studyIsabelle Le Ber, Agnès Camuzat, Didier Hannequin, et al.
Neurobiology of Aging|March 16, 2020
Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experienceLeila Sellami, Benoît Rucheton, Imen Ben Younes, et al.
Brain : a Journal of Neurology|September 26, 2013
Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, Camille Charbonnier, et al.
The Journal of Clinical Investigation|December 15, 2023
Rational design of a SOCS1-edited tumor-infiltrating lymphocyte therapy using CRISPR/Cas9 screensMichael R Schlabach, Sharon Lin, Zachary R Collester, et al.
Nature Medicine|May 14, 2024
Progranulin AAV gene therapy for frontotemporal dementia: translational studies and phase 1/2 trial interim resultsJeffrey Sevigny, Olga Uspenskaya, Laura Dean Heckman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 6, 2021
Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohortGeorgia Peakman, Lucy L Russell, Rhian S Convery, et al.
Pageof 48

Showing results (371-380 of 473) with videos related to

Sort By:
Pageof 48
Brain : a Journal of Neurology|November 15, 2025
The genetic landscape of frontotemporal lobar degeneration: investigation of a diagnostic cohort of 2747 probandsGuillaume Cogan, Marion Houot, Julie Bogoin, et al.
BMC Research Notes|October 2, 2023
RNAseq based variant dataset in a black poplar association panelOdile Rogier, Aurélien Chateigner, Marie-Claude Lesage-Descauses, et al.
Brain : a Journal of Neurology|November 17, 2021
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxiaMarie Coutelier, Maxime Jacoupy, Alexandre Janer, et al.
Journal of Alzheimer'S Disease : JAD|April 6, 2012
The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkersDavid Wallon, Stéphane Rousseau, Anne Rovelet-Lecrux, et al.
Brain : a Journal of Neurology|February 5, 2008
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic studyIsabelle Le Ber, Agnès Camuzat, Didier Hannequin, et al.
Neurobiology of Aging|March 16, 2020
Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experienceLeila Sellami, Benoît Rucheton, Imen Ben Younes, et al.
Brain : a Journal of Neurology|September 26, 2013
Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, Camille Charbonnier, et al.
The Journal of Clinical Investigation|December 15, 2023
Rational design of a SOCS1-edited tumor-infiltrating lymphocyte therapy using CRISPR/Cas9 screensMichael R Schlabach, Sharon Lin, Zachary R Collester, et al.
Nature Medicine|May 14, 2024
Progranulin AAV gene therapy for frontotemporal dementia: translational studies and phase 1/2 trial interim resultsJeffrey Sevigny, Olga Uspenskaya, Laura Dean Heckman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 6, 2021
Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohortGeorgia Peakman, Lucy L Russell, Rhian S Convery, et al.
Pageof 48