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

Patrick Santens

Showing results (101-110 of 123) with videos related to

Pageof 13
Sort By:
Neurology|January 21, 2018
Teenage-onset progressive myoclonic epilepsy due to a familial <i>C9orf72</i> repeat expansionJelle van den Ameele, Ivana Jedlickova, Anna Pristoupilova, et al.
Human Molecular Genetics|October 25, 2007
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroJulie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, et al.
Neurobiology of Aging|November 1, 2011
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohortsTim Van Langenhove, Julie van der Zee, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology|March 1, 2011
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohortJulie van der Zee, Tim Van Langenhove, Gernot Kleinberger, et al.
Journal of Neuropathology and Experimental Neurology|February 27, 2021
Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets NeurodegenerationAnne Sieben, Tim Van Langenhove, Yannick Vermeiren, et al.
Parkinsonism & Related Disorders|December 13, 2005
Deep brain stimulation of the internal pallidum in multiple system atrophyPatrick Santens, Santens Patrick, Kristl Vonck, et al.
Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology|February 24, 2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLDJulie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
Neurology. Genetics|May 8, 2023
Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic DisordersNika Schuermans, Hannah Verdin, Jody Ghijsels, et al.
Alzheimer'S Research & Therapy|January 27, 2018
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one familyAnne Sieben, Sara Van Mossevelde, Eline Wauters, et al.
Pageof 13

Showing results (101-110 of 123) with videos related to

Sort By:
Pageof 13
Neurology|January 21, 2018
Teenage-onset progressive myoclonic epilepsy due to a familial <i>C9orf72</i> repeat expansionJelle van den Ameele, Ivana Jedlickova, Anna Pristoupilova, et al.
Human Molecular Genetics|October 25, 2007
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroJulie van der Zee, Hazel Urwin, Sebastiaan Engelborghs, et al.
Neurobiology of Aging|November 1, 2011
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohortsTim Van Langenhove, Julie van der Zee, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology|March 1, 2011
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohortJulie van der Zee, Tim Van Langenhove, Gernot Kleinberger, et al.
Journal of Neuropathology and Experimental Neurology|February 27, 2021
Hippocampal Sclerosis in Frontotemporal Dementia: When Vascular Pathology Meets NeurodegenerationAnne Sieben, Tim Van Langenhove, Yannick Vermeiren, et al.
Parkinsonism & Related Disorders|December 13, 2005
Deep brain stimulation of the internal pallidum in multiple system atrophyPatrick Santens, Santens Patrick, Kristl Vonck, et al.
Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology|February 24, 2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLDJulie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, et al.
Neurology. Genetics|May 8, 2023
Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic DisordersNika Schuermans, Hannah Verdin, Jody Ghijsels, et al.
Alzheimer'S Research & Therapy|January 27, 2018
Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one familyAnne Sieben, Sara Van Mossevelde, Eline Wauters, et al.
Pageof 13