au.\*:("GIJSELINCK, Ilse")
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Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson diseaseTHEUNS, Jessie; VERSTRAETEN, Aline; KRÜGER, Rejko et al.Neurology. 2014, Vol 83, Num 21, pp 1906-1913, issn 0028-3878, 8 p.Article
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
Identification of 2 Loci at Chromosomes 9 and 14 in a Multiplex Family With Frontotemporal Lobar Degeneration and Amyotrophic Lateral SclerosisGIJSELINCK, Ilse; ENGELBORGHS, Sebastiaan; KUMAR-SINGH, Samir et al.Archives of neurology (Chicago). 2010, Vol 67, Num 5, pp 606-616, issn 0003-9942, 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
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathySLEEGERS, Kristel; BROUWERS, Nathalie; GIJSELINCK, Ilse et al.Brain. 2006, Vol 129, pp 2977-2983, issn 0006-8950, 7 p., 11Article
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau regionCRUTS, Marc; RADEMAKERS, Rosa; GIJSELINCK, Ilse et al.Human molecular genetics (Print). 2005, Vol 14, Num 13, pp 1753-1762, issn 0964-6906, 10 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
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