Invited Article : The Alzheimer disease-frontotemporal lobar degeneration spectrumVAN DER ZEE, Julie; SLEEGERS, Kristel; VAN BROECKHOVEN, Christine et al.Neurology. 2008, Vol 71, Num 15, pp 1191-1197, issn 0028-3878, 7 p.Article

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

Phenotype variability in progranulin mutation carriers : a clinical, neuropsychological, imaging and genetic studyLE BER, Isabelle; CAMUZAT, Agnès; PUEL, Michèle et al.Brain. 2008, Vol 131, pp 732-746, issn 0006-8950, 15 p., 3Article

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

No association of PGRN 3'UTR rs5848 in frontotemporal lobar degenerationROLLINSON, Sara; ROHRER, Jonathan D; PICKERING-BROWN, Stuart M et al.Neurobiology of aging. 2011, Vol 32, Num 4, pp 754-755, issn 0197-4580, 2 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

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

Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid LipofuscinosisNOSKOVA, Lenka; STRANECKY, Viktor; SIMS, Katherine B et al.American journal of human genetics. 2011, Vol 89, Num 2, pp 241-252, issn 0002-9297, 12 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

Common variants at 7p21 are associated with fronto- temporal lobar degeneration with TDP-43 inclusionsVAN DEERLIN, Vivianna M; SLEIMAN, Patrick M. A; ARNOLD, Steven E et al.Nature genetics. 2010, Vol 42, Num 3, pp 234-239, issn 1061-4036, 6 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

A novel locus for dementia with Lewy bodies : a clinically and genetically heterogeneous disorderBOGAERTS, Veerle; ENGELBORGHS, Sebastiaan; GASSER, Thomas et al.Brain. 2007, Vol 130, pp 2277-2291, issn 0006-8950, 15 p., 9Article

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