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

An Goris

Showing results (51-60 of 86) with videos related to

Pageof 9
Sort By:
Human Molecular Genetics|October 16, 2012
Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiencyRobin Lemmens, Alessandra Maugeri, Hans W M Niessen, et al.
Brain : a Journal of Neurology|October 9, 2009
The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohortCaroline H Williams-Gray, Jonathan R Evans, An Goris, et al.
Human Molecular Genetics|February 21, 2012
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosisSarah Herdewyn, Hui Zhao, Matthieu Moisse, et al.
Neuroscience Letters|November 1, 2005
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosisChiara Fenoglio, Daniela Galimberti, Maria Ban, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|May 28, 2016
Immunologic profiles of multiple sclerosis treatments reveal shared early B cell alterationsJames Dooley, Ine Pauwels, Dean Franckaert, et al.
Journal of Neuroimmunology|September 2, 2018
LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patientsChiara Fenoglio, Emanuela Oldoni, Maria Serpente, et al.
Annals of Neurology|August 9, 2007
Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's diseaseAn Goris, Caroline H Williams-Gray, Graeme R Clark, et al.
Brain : a Journal of Neurology|January 24, 2018
Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cellsIde Smets, Barnaby Fiddes, Josselyn E Garcia-Perez, et al.
Human Molecular Genetics|July 6, 2016
Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A miceKim A Staats, Stephanie Humblet-Baron, Andre Bento-Abreu, et al.
Annals of Neurology|March 14, 2013
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosisNadia Barizzone, Ine Pauwels, Bernadetta Luciano, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|October 16, 2012
Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiencyRobin Lemmens, Alessandra Maugeri, Hans W M Niessen, et al.
Brain : a Journal of Neurology|October 9, 2009
The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohortCaroline H Williams-Gray, Jonathan R Evans, An Goris, et al.
Human Molecular Genetics|February 21, 2012
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosisSarah Herdewyn, Hui Zhao, Matthieu Moisse, et al.
Neuroscience Letters|November 1, 2005
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosisChiara Fenoglio, Daniela Galimberti, Maria Ban, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|May 28, 2016
Immunologic profiles of multiple sclerosis treatments reveal shared early B cell alterationsJames Dooley, Ine Pauwels, Dean Franckaert, et al.
Journal of Neuroimmunology|September 2, 2018
LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patientsChiara Fenoglio, Emanuela Oldoni, Maria Serpente, et al.
Annals of Neurology|August 9, 2007
Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's diseaseAn Goris, Caroline H Williams-Gray, Graeme R Clark, et al.
Brain : a Journal of Neurology|January 24, 2018
Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cellsIde Smets, Barnaby Fiddes, Josselyn E Garcia-Perez, et al.
Human Molecular Genetics|July 6, 2016
Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A miceKim A Staats, Stephanie Humblet-Baron, Andre Bento-Abreu, et al.
Annals of Neurology|March 14, 2013
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosisNadia Barizzone, Ine Pauwels, Bernadetta Luciano, et al.
Pageof 9