about
Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiencyWhole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosisProgressive multifocal leukoencephalopathy after natalizumab therapy for Crohn's diseaseHot-spot residue in small heat-shock protein 22 causes distal motor neuropathyDisrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathyITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyAge of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.Prevention of intestinal obstruction reveals progressive neurodegeneration in mutant TDP-43 (A315T) mice.Synaptopodin and 4 novel genes identified in primary sensory neurons.Development of Improved HDAC6 Inhibitors as Pharmacological Therapy for Axonal Charcot-Marie-Tooth DiseaseExome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathyProgranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathyModelling amyotrophic lateral sclerosis: progress and possibilitiesAnalysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyRare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationC9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisPolymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisMapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common strokeEfficacy and safety of xaliproden in amyotrophic lateral sclerosis: results of two phase III trials.Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.VEGF modulates NMDA receptors activity in cerebellar granule cells through Src-family kinases before synapse formation.Noninvasive ventilation improves sleep in amyotrophic lateral sclerosis: a prospective polysomnographic study.A yeast functional screen predicts new candidate ALS disease genesChromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity.The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival.Heterogeneity in motoneuron disease.Deletion or Inhibition of the Oxygen Sensor PHD1 Protects against Ischemic Stroke via Reprogramming of Neuronal Metabolism.Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degenerationBenefits of intensive insulin therapy on neuromuscular complications in routine daily critical care practice: a retrospective study.Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A mice.No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.ATXN2 trinucleotide repeat length correlates with risk of ALS.TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.Guidelines for preclinical animal research in ALS/MND: A consensus meeting.
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description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
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name
Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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type
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Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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prefLabel
Wim Robberecht
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Wim Robberecht
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Wim Robberecht
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Wim Robberecht
@fr
Wim Robberecht
@nl
Wim Robberecht
@sl