Wim Robberecht Department of Neurosciences, Experimental Neurology KU Leuven - University of Leuven Biography Publications Institution JoVE Articles Wim Robberecht has not added a biography. If you are Wim Robberecht and would like to personalize this page please email our Author Liaison for assistance. Publications Conditional Deletion of Id2 or Notch1 in Oligodendrocyte Progenitor Cells Does Not Ameliorate Disease Outcome in SOD1 Mice Neurobiology of Aging. Aug, 2018 | Pubmed ID: 29689424 Genome-wide Analyses Identify KIF5A As a Novel ALS Gene Neuron. Mar, 2018 | Pubmed ID: 29566793 HDAC6 is a Therapeutic Target in Mutant GARS-induced Charcot-Marie-Tooth Disease Brain : a Journal of Neurology. Feb, 2018 | Pubmed ID: 29415205 Elongator Subunit 3 (ELP3) Modifies ALS Through TRNA Modification Human Molecular Genetics. Apr, 2018 | Pubmed ID: 29415125 A Zebrafish Model for C9orf72 ALS Reveals RNA Toxicity As a Pathogenic Mechanism Acta Neuropathologica. Mar, 2018 | Pubmed ID: 29302778 Reconsidering the Causality of TIA1 Mutations in ALS Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 02, 2018 | Pubmed ID: 29235362 Inhibition of Histone Deacetylase 6 (HDAC6) Protects Against Vincristine-induced Peripheral Neuropathies and Inhibits Tumor Growth Neurobiology of Disease. Mar, 2018 | Pubmed ID: 29197621 Amyotrophic Lateral Sclerosis Nature Reviews. Disease Primers. Oct, 2017 | Pubmed ID: 28980624 Prognostic Value of Clinical and Electrodiagnostic Parameters at Time of Diagnosis in Patients with Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Aug, 2017 | Pubmed ID: 28631957 Identification and Characterization of Nanobodies Targeting the EphA4 Receptor The Journal of Biological Chemistry. 07, 2017 | Pubmed ID: 28526745 Progranulin Functions As a Cathepsin D Chaperone to Stimulate Axonal Outgrowth in Vivo Human Molecular Genetics. 08, 2017 | Pubmed ID: 28453791 Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule Dynamics Molecular Cell. Mar, 2017 | Pubmed ID: 28306503 ATXN2 Trinucleotide Repeat Length Correlates with Risk of ALS Neurobiology of Aging. Mar, 2017 | Pubmed ID: 28017481 C9orf72 Expansion Differentially Affects Males with Spinal Onset Amyotrophic Lateral Sclerosis Journal of Neurology, Neurosurgery, and Psychiatry. Apr, 2017 | Pubmed ID: 27663272 Genome-wide Association Analyses Identify New Risk Variants and the Genetic Architecture of Amyotrophic Lateral Sclerosis Nature Genetics. Sep, 2016 | Pubmed ID: 27455348 Genetic Ablation of IP3 Receptor 2 Increases Cytokines and Decreases Survival of SOD1G93A Mice Human Molecular Genetics. 08, 2016 | Pubmed ID: 27378687 Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis JAMA Neurology. Jul, 2016 | Pubmed ID: 27244217 Prospective Validation of 18F-FDG Brain PET Discriminant Analysis Methods in the Diagnosis of Amyotrophic Lateral Sclerosis Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine. Aug, 2016 | Pubmed ID: 26940764 Drosophila Screen Connects Nuclear Transport Genes to DPR Pathology in C9ALS/FTD Scientific Reports. Feb, 2016 | Pubmed ID: 26869068 Modifiers of C9orf72 Dipeptide Repeat Toxicity Connect Nucleocytoplasmic Transport Defects to FTD/ALS Nature Neuroscience. Sep, 2015 | Pubmed ID: 26308983 Cochlear Supporting Cell Transdifferentiation and Integration into Hair Cell Layers by Inhibition of Ephrin-B2 Signalling Nature Communications. Apr, 2015 | Pubmed ID: 25923646 The Role of Oligodendroglial Dysfunction in Amyotrophic Lateral Sclerosis Neurodegenerative Disease Management. 2014 | Pubmed ID: 25095817 Prevention of Intestinal Obstruction Reveals Progressive Neurodegeneration in Mutant TDP-43 (A315T) Mice Molecular Neurodegeneration. Jun, 2014 | Pubmed ID: 24938805 Developments in Treatments for Amyotrophic Lateral Sclerosis Via Intracerebroventricular or Intrathecal Delivery Expert Opinion on Investigational Drugs. Jul, 2014 | Pubmed ID: 24816247 In Vivo Électrophysiologique mesure du potentiel d’Action musculaire composé de membres antérieurs dans des modèles murins de la dégénérescence des motoneurones Eveliina Pollari1,2, Robert Prior1,2, Wim Robberecht1,2,3, Philip Van Damme1,2,3, Ludo Van Den Bosch1,2 1Department of Neurosciences, Experimental Neurology, KU Leuven - University of Leuven, 2Center for Brain & Disease Research, Laboratory of Neurobiology, VIB, 3Department of Neurology, University Hospitals Leuven JoVE 57741 Neuroscience
In Vivo Électrophysiologique mesure du potentiel d’Action musculaire composé de membres antérieurs dans des modèles murins de la dégénérescence des motoneurones Eveliina Pollari1,2, Robert Prior1,2, Wim Robberecht1,2,3, Philip Van Damme1,2,3, Ludo Van Den Bosch1,2 1Department of Neurosciences, Experimental Neurology, KU Leuven - University of Leuven, 2Center for Brain & Disease Research, Laboratory of Neurobiology, VIB, 3Department of Neurology, University Hospitals Leuven JoVE 57741 Neuroscience
