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

D Rohrer

Showing results (331-340 of 482) with videos related to

Pageof 49
Sort By:
Neurobiology of Aging|November 25, 2017
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI studyDavid M Cash, Martina Bocchetta, David L Thomas, et al.
Neurology|February 14, 2025
Montreal Cognitive Assessment vs the Mini-Mental State Examination as a Screening Tool for Patients With Genetic Frontotemporal DementiaLiset de Boer, Jackie M Poos, Esther Van Den Berg, et al.
Neuroimage. Clinical|May 23, 2017
White matter hyperintensities are seen only in <i>GRN</i> mutation carriers in the GENFI cohortCarole H Sudre, Martina Bocchetta, David Cash, et al.
Neurology|February 18, 2011
Classification of primary progressive aphasia and its variantsM L Gorno-Tempini, A E Hillis, S Weintraub, et al.
Brain : a Journal of Neurology|September 13, 2011
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Jonathan M Schott, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association studyWilliam J Scotton, Rebecca R Valentino, Alejandro Martinez-Carrasco, et al.
Neuroimage|December 12, 2018
Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohortClaire Cury, Stanley Durrleman, David M Cash, et al.
Molecular Neurodegeneration|November 28, 2021
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI studySofia Bergström, Linn Öijerstedt, Julia Remnestål, et al.
Nature Reviews. Neurology|June 22, 2019
SILK studies - capturing the turnover of proteins linked to neurodegenerative diseasesRoss W Paterson, Audrey Gabelle, Brendan P Lucey, 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 49

Showing results (331-340 of 482) with videos related to

Sort By:
Pageof 49
Neurobiology of Aging|November 25, 2017
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI studyDavid M Cash, Martina Bocchetta, David L Thomas, et al.
Neurology|February 14, 2025
Montreal Cognitive Assessment vs the Mini-Mental State Examination as a Screening Tool for Patients With Genetic Frontotemporal DementiaLiset de Boer, Jackie M Poos, Esther Van Den Berg, et al.
Neuroimage. Clinical|May 23, 2017
White matter hyperintensities are seen only in <i>GRN</i> mutation carriers in the GENFI cohortCarole H Sudre, Martina Bocchetta, David Cash, et al.
Neurology|February 18, 2011
Classification of primary progressive aphasia and its variantsM L Gorno-Tempini, A E Hillis, S Weintraub, et al.
Brain : a Journal of Neurology|September 13, 2011
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Jonathan M Schott, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association studyWilliam J Scotton, Rebecca R Valentino, Alejandro Martinez-Carrasco, et al.
Neuroimage|December 12, 2018
Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohortClaire Cury, Stanley Durrleman, David M Cash, et al.
Molecular Neurodegeneration|November 28, 2021
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI studySofia Bergström, Linn Öijerstedt, Julia Remnestål, et al.
Nature Reviews. Neurology|June 22, 2019
SILK studies - capturing the turnover of proteins linked to neurodegenerative diseasesRoss W Paterson, Audrey Gabelle, Brendan P Lucey, 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 49