about
Diagnosis-independent Alzheimer disease biomarker signature in cognitively normal elderly peopleGenome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseThe genetics and neuropathology of frontotemporal lobar degenerationRecurrent transient ischemic attacks in a 15-year-old boy with beta-thalassemia minor and thrombophilia. Contribution of perfusion SPECT to clinical diagnosisNull mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Cerebrospinal Fluid Biomarkers for Alzheimer's Disease: A View of the Regulatory Science Qualification Landscape from the Coalition Against Major Diseases CSF Biomarker TeamThe CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study.Advancing research diagnostic criteria for Alzheimer's disease: the IWG-2 criteria.Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationA Practical Guide to Immunoassay Method ValidationMonitoring of physical activity after stroke: a systematic review of accelerometry-based measures.Disrupted auto-activation, dysexecutive and confabulating syndrome following bilateral thalamic and right putaminal strokeConsensus guidelines for lumbar puncture in patients with neurological diseases.A foreign speech accent in a case of conversion disorder.No added diagnostic value of non-phosphorylated tau fraction (p-taurel) in CSF as a biomarker for differential dementia diagnosis.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationCerebellar-induced apraxic agraphia: a review and three new cases.Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson diseaseTMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohortPromoter mutations that increase amyloid precursor-protein expression are associated with Alzheimer disease.Cerebellar cognitive affective syndrome without global mental retardation in two relatives with Gillespie syndrome.Foreign accent syndrome as a developmental motor speech disorder.Tau monoclonal antibody generation based on humanized yeast models: impact on Tau oligomerization and diagnosticsThe monoaminergic footprint of depression and psychosis in dementia with Lewy bodies compared to Alzheimer's disease.TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodiesCerebrospinal Fluid P-Tau181P: Biomarker for Improved Differential Dementia Diagnosis.Prevalence of cerebral amyloid pathology in persons without dementia: a meta-analysis.Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk.Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.Reduced secreted clusterin as a mechanism for Alzheimer-associated CLU mutations.sTREM2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early-stage Alzheimer's disease and associate with neuronal injury markers.Recommendations for the treatment of epilepsy in adult patients in general practice in Belgium: an update.Lipocalin 2: novel component of proinflammatory signaling in Alzheimer's disease.Alzheimer's disease cerebrospinal fluid biomarker in cognitively normal subjects.Diagnostic value of MIBG cardiac scintigraphy for differential dementia diagnosis.Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.
P50
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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type
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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Sebastiaan Engelborghs
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P106
P21
P31
P496
0000-0003-0304-9785