Parcellation of parietal cortex : Convergence between lesion-symptom mapping and mapping of the intact functioning brainVANDENBERGHE, Rik; GILLEBERT, Céline R.Behavioural brain research. 2009, Vol 199, Num 2, pp 171-182, issn 0166-4328, 12 p.Article

Anterior temporal laterality in primary progressive aphasia shifts to the rightVANDENBULCKE, Mathieu; PEETERS, Ronald; VAN HECKE, Paul et al.Annals of neurology. 2005, Vol 58, Num 3, pp 362-370, issn 0364-5134, 9 p.Article

Astronomia nova to human brain mappingVANDENBERGHE, Rik.Neural networks. 2006, Vol 19, Num 9, pp 1453-1454, issn 0893-6080, 2 p.Article

The associative-semantic network for words and pictures: Effective connectivity and graph analysis : THE DUAL LOOP MODEL IN LANGUAGE AND OTHER MODALITIES: AN INTERDISCIPLINARY APPROACHVANDENBERGHE, Rik; YU WANG; NELISSEN, Natalie et al.Brain and language (Print). 2013, Vol 127, Num 2, pp 264-272, issn 0093-934X, 9 p.Article

Lesion evidence for the critical role of the intraparietal sulcus in spatial attentionGILLEBERT, Céline R; MANTINI, Dante; THIJS, Vincent et al.Brain. 2011, Vol 134, pp 1694-1709, issn 0006-8950, 16 p., 6Article

Cytoarchitectonic mapping of attentional selection and reorienting in parietal cortexGILLEBERT, Céline R; MANTINI, Dante; PEETERS, Ronald et al.NeuroImage (Orlando, Fla.). 2013, Vol 67, pp 257-272, issn 1053-8119, 16 p.Article

Lesion neuroanatomy of the Sustained Attention to Response taskMOLENBERGHS, Pascal; GILLEBERT, Céline R; SCHOOFS, Hanne et al.Neuropsychologia. 2009, Vol 47, Num 13, pp 2866-2875, issn 0028-3932, 10 p.Article

Spatial attention deficits in humans: The critical role of superior compared to inferior parietal lesionsVANDENBERGHE, Rik; MOLENBERGHS, Pascal; GILLEBERT, Céline R et al.Neuropsychologia. 2012, Vol 50, Num 6, pp 1092-1103, issn 0028-3932, 12 p.Article

Recherche empirique d'un substrat neuronal aux processus cognitifs impliqués dans différentes tâches de flexibilité = Empirical search forneural correlates of cognitive subcomponents in different shifting tasksSALMON, Eric; VAN DER LINDEN, Martial; VANDENBERGHE, Rik et al.Revue de neuropsychologie, neurosciences cognitives et cliniques. 2010, Vol 2, Num 1, pp 11-21, issn 2101-6739, 11 p.Article

A belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD. CommentaryHARDY, John; MOMENI, Parastoo; CAEKEBEKE, Jo et al.Brain. 2006, Vol 129, issn 0006-8950, 830-831,841-852 [14 p.], 4Article

Cognitive deficits during status epilepticus and time course of recovery : A case reportVAN PAESSCHEN, Wim; PORKE, Kathleen; FANNES, Katrien et al.Epilepsia (Copenhagen). 2007, Vol 48, Num 10, pp 1979-1983, issn 0013-9580, 5 p.Article

Noun and knowledge retrieval for biological and non-biological entities following right occipitotemporal lesionsBRUFFAERTS, Rose; DE WEER, An-Sofie; VANDENBERGHE, Rik et al.Neuropsychologia. 2014, Vol 62, pp 163-174, issn 0028-3932, 12 p.Article

Binary classification of ¹⁸F-flutemetamol PET using machine learning: Comparison with visual reads and structural MRIVANDENBERGHE, Rik; NELISSEN, Natalie; DUPONT, Patrick et al.NeuroImage (Orlando, Fla.). 2013, Vol 64, pp 517-525, issn 1053-8119, 9 p.Article

Microglial Upregulation of Progranulin as a Marker of Motor Neuron DegenerationPHILIPS, Thomas; DE MUYNCK, Louis; SCIOT, Raf et al.Journal of neuropathology and experimental neurology. 2010, Vol 69, Num 12, pp 1191-1200, issn 0022-3069, 10 p.Article

Aβ amyloid deposition in the language system and how the brain respondsNELISSEN, Natalie; VANDENBULCKE, Mathieu; FANNES, Katrien et al.Brain. 2007, Vol 130, pp 2055-2069, issn 0006-8950, 15 p., 8Article

Reduced expression of hsa-miR-27a-3p in CSF of patients with Alzheimer diseaseFRIGERIO, Carlo Sala; LAU, Pierre; DE STROOPER, Bart et al.Neurology. 2013, Vol 81, Num 24, pp 2103-2106, issn 0028-3878, 4 p.Article

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohortVAN DER ZEE, Julie; VAN LANGENHOVE, Tim; MATTHEIJSSENS, Maria et al.Brain. 2011, Vol 134, pp 808-815, issn 0006-8950, 8 p., 3Article

Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSGIJSELINCK, Ilse; SLEEGERS, Kristel; DE POOTER, Tim et al.Neurobiology of aging. 2009, Vol 30, Num 8, pp 1329-1331, issn 0197-4580, 3 p.Article

Alzheimer and parkinson diagnoses in progranulin null mutation carriers in an extended founder familyBROUWERS, Nathalie; NUYTEMANS, Karen; BOGAERTS, Veerle et al.Archives of neurology (Chicago). 2007, Vol 64, Num 10, pp 1436-1446, issn 0003-9942, 11 p.Article

Autoimmune-mediated encephalitisDEMAEREL, Philippe; VAN DESSEL, Wim; VAN PAESSCHEN, Wim et al.Neuroradiology (Berlin. Print). 2011, Vol 53, Num 11, pp 837-851, issn 0028-3940, 15 p.Article

Serum Biomarker for Progranulin-Associated Frontotemporal Lobar DegenerationSLEEGERS, Kristel; BROUWERS, Nathalie; DE DEYN, Peter P et al.Annals of neurology. 2009, Vol 65, Num 5, pp 603-609, issn 0364-5134, 7 p.Article

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitroVAN DER ZEE, Julie; URWIN, Hazel; FISHER, Elizabeth M et al.Human molecular genetics (Print). 2008, Vol 17, Num 2, pp 313-322, issn 0964-6906, 10 p.Article

Characterization of ubiquitinated intraneuronal inclusions in a novel belgian frontotemporal lobar degeneration familyPIRICI, Daniel; VANDENBERGHE, Rik; VAN BROECKHOVEN, Christine et al.Journal of neuropathology and experimental neurology. 2006, Vol 65, Num 3, pp 289-301, issn 0022-3069, 13 p.Article

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21CRUTS, Marc; GIJSELINCK, Ilse; VAN DUIJN, Cornelia et al.Nature (London). 2006, Vol 442, Num 7105, pp 920-924, issn 0028-0836, 5 p.Article

Paradoxical features of word finding difficulty in primary progressive aphasiaVANDENBERGHE, Rik R; VANDENBULCKE, Mathieu; WEINTRAUB, Sandra et al.Annals of neurology. 2005, Vol 57, Num 2, pp 204-209, issn 0364-5134, 6 p.Article