Organisation
Laboratory for Cognitive Neurology
Lab
The research of the Laboratory for Cognitive Neurology focuses on cognitive domains selective attention, language and semantic memory.
Current researchers
1 - 10 of 12 results
- Rik Vandenberghe (Responsible)
- Helena Balabin (Member)
- Patrick Dupont (Member)
- Tarik Jamoulle (Member)
- Antonietta Gabriella Liuzzi (Member)
- Gabriela Meade (Member)
- Mariska Reinartz (Member)
- Jolien Schaeverbeke (Member)
- Laure Spruyt (Member)
- Kevin Statz (Member)
Projects
1 - 10 of 65
- Peripheral blood T cell tracing and metabolomic analysis for diagnosis of Alzheimer's diseaseFrom19 Dec 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Engelstalig: precision medicine en care in patients neuromuscular dystrophyFrom7 Nov 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- The aging T-Cell immune system, cognitive aging and Alzheimer's diseaseFrom4 Oct 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- The neurobiology of meaning composition: a multi-method research approachFrom1 Oct 2023 → TodayFunding: FWO senior postdoctoral fellowship
- In vivo PET of synaptic density in cognitive disorders: prospective evaluation of neuronal dysfunction and relation to symptomatology.From1 Oct 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Natural Language Processing analysis of connected speech in Alzheimer disease and related disordersFrom1 Jan 2023 → TodayFunding: Foundations, funds and other with scientific goal
- Selective vulnerability in Alzheimer’s disease and frontotemporal degeneration: integration of postmortem MRI, mass-spectrometry and histopathologyFrom1 Oct 2022 → TodayFunding: FWO senior postdoctoral fellowship
- Evaluating novel radiological and clinical outcome measures in hereditary neuromuscular diseases.From1 Jun 2022 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- blood-based makers for neurodegeneration in early stages of Alzheimer’s diseaseFrom1 Apr 2022 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Disease-associated proteome alternations in semantic variant primary progressive aphasia.From1 Jan 2022 → 31 Dec 2023Funding: Private funding of national origin - undefined
Publications
441 - 450 of 562
- Occipital lobe epilepsy, myoclonus, refractory status epilepticus, ataxia and polyneuropathy represent the core features of a syndrome caused by POLG1 mutations(2009)
Authors: A Quaegebeur, G Van Goethem, K Smets, P De Jonghe, Rik Vandenberghe, Wim Van Paesschen
Pages: S74 - S74 - Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis(2021)
Authors: Rik Vandenberghe
- Binding of [18F]AV1451 in post mortem brain slices of semantic variant primary progressive aphasia patients(2020)
Authors: Jolien Schaeverbeke, Sofie Celen, Koen Van Laere, Dietmar Thal, Thomas Tousseyn, Guy Bormans, Rik Vandenberghe
Pages: 1949 - 1960 - Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traits(2023)
Authors: Rik Vandenberghe
- A metabolite-based machine learning approach to diagnose Alzheimer-type dementia in blood: Results from the European Medical Information Framework for Alzheimer disease biomarker discovery cohort(2019)
Authors: Rik Vandenberghe, Karen Meersmans
Pages: 933 - 938 - Friend or foe? Flankers reverse the direction of orthographic neighbourhood effects(2020)
Authors: Gabriela Meade, Jonathan Grainger, Mathieu Declerck
Pages: 535 - 542 - Preliminary evidence for preserved synaptic density in late-life depression.(2024)
Authors: Thomas Vande Casteele, Maarten Laroy, Margot Van Cauwenberge, Patrick Dupont, Jan Van den Stock, Filip Bouckaert, Louise Emsell, Mathieu Vandenbulcke
Pages: 145 - TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis(2017)
Authors: Rik Vandenberghe, Wim Robberecht, Philip Van Damme
Pages: 297 - 309 - Small Molecules Can Rescue Progranulin Haploinsufficiency Underlying Frontotemporal Lobar Degeneration Caused by GRN mutations(2012)
Authors: Louis De Muynck, Susanna Raitano, Martine Geraerts, Rik Vandenberghe, Dominique Audenaert, Ludo Van Den Bosch, Michele M Maxwell, Aleksey G Kazantsev, Robert Brown Jr, Wim Robberecht, et al.
Pages: 271 - 272 - Serum biomarker for progranulin-associated frontotemporal lobar degeneration(2009)
Authors: Philip Van Damme, Rik Vandenberghe, Wim Robberecht
Pages: 603 - 609