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

Dimitri Hemelsoet

Showing results (61-70 of 84) with videos related to

Pageof 9
Sort By:
Acta Cardiologica|April 20, 2022
Lipid-lowering therapy and risk-based LDL-C goal attainment in Belgium: DA VINCI observational studyPhilippe van de Borne, André Peeters, Luc Janssens, et al.
Scientific Reports|December 12, 2025
Increased plasma fibronectin mirrors intimal phenotypic switching of vascular smooth muscle cells in moyamoya arteriopathyCaroline Asselman, Jozefien Meersschaut, Patrick Willems, et al.
Cell Host & Microbe|September 1, 2019
HIV Rebound Is Predominantly Fueled by Genetically Identical Viral Expansions from Diverse ReservoirsMarie-Angélique De Scheerder, Bram Vrancken, Simon Dellicour, 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.
Orphanet Journal of Rare Diseases|May 23, 2022
Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, et al.
Clinical Neurology and Neurosurgery|December 11, 2012
Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the youngIsabel De Brabander, Laetitia Yperzeele, Chantal Ceuterick-De Groote, et al.
Journal of Clinical Immunology|March 23, 2022
Mutations in RNU7-1 Weaken Secondary RNA Structure, Induce MCP-1 and CXCL10 in CSF, and Result in Aicardi-Goutières Syndrome with Severe End-Organ InvolvementLeslie Naesens, Josephine Nemegeer, Filip Roelens, et al.
Journal of Stroke|June 4, 2026
Outcomes of Early Versus Later Anticoagulation in Asian Atrial Fibrillation-Related Stroke: ELAN Subgroup AnalysisTakeshi Yoshimoto, Masafumi Ihara, P N Sylaja, et al.
Frontiers in Neurology|June 26, 2020
Prior Stroke in PFO Patients Is Associated With Both PFO-Related and -Unrelated FactorsTimo Kahles, Patrik Michel, Alexander Hapfelmeier, et al.
Intensive Care Medicine|September 19, 2024
Publisher Correction: Coaching doctors to improve ethical decision-making in adult hospitalized patients potentially receiving excessive treatment. The CODE stepped-wedge cluster randomized controlled trialDominique D Benoit, Aglaja De Pauw, Celine Jacobs, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Acta Cardiologica|April 20, 2022
Lipid-lowering therapy and risk-based LDL-C goal attainment in Belgium: DA VINCI observational studyPhilippe van de Borne, André Peeters, Luc Janssens, et al.
Scientific Reports|December 12, 2025
Increased plasma fibronectin mirrors intimal phenotypic switching of vascular smooth muscle cells in moyamoya arteriopathyCaroline Asselman, Jozefien Meersschaut, Patrick Willems, et al.
Cell Host & Microbe|September 1, 2019
HIV Rebound Is Predominantly Fueled by Genetically Identical Viral Expansions from Diverse ReservoirsMarie-Angélique De Scheerder, Bram Vrancken, Simon Dellicour, 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.
Orphanet Journal of Rare Diseases|May 23, 2022
Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, et al.
Clinical Neurology and Neurosurgery|December 11, 2012
Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the youngIsabel De Brabander, Laetitia Yperzeele, Chantal Ceuterick-De Groote, et al.
Journal of Clinical Immunology|March 23, 2022
Mutations in RNU7-1 Weaken Secondary RNA Structure, Induce MCP-1 and CXCL10 in CSF, and Result in Aicardi-Goutières Syndrome with Severe End-Organ InvolvementLeslie Naesens, Josephine Nemegeer, Filip Roelens, et al.
Journal of Stroke|June 4, 2026
Outcomes of Early Versus Later Anticoagulation in Asian Atrial Fibrillation-Related Stroke: ELAN Subgroup AnalysisTakeshi Yoshimoto, Masafumi Ihara, P N Sylaja, et al.
Frontiers in Neurology|June 26, 2020
Prior Stroke in PFO Patients Is Associated With Both PFO-Related and -Unrelated FactorsTimo Kahles, Patrik Michel, Alexander Hapfelmeier, et al.
Intensive Care Medicine|September 19, 2024
Publisher Correction: Coaching doctors to improve ethical decision-making in adult hospitalized patients potentially receiving excessive treatment. The CODE stepped-wedge cluster randomized controlled trialDominique D Benoit, Aglaja De Pauw, Celine Jacobs, et al.
Pageof 9