Loss of progranulin function in frontotemporal lobar degenerationCRUTS, Marc; VAN BROECKHOVEN, Christine.Trends in genetics (Regular ed.). 2008, Vol 24, Num 4, pp 186-194, issn 0168-9525, 9 p.Article

Molecular Pathways of Frontotemporal Iobar DegetierationSLEEGERS, Kristel; CRUTS, Marc; VAN BROECKHOVEN, Christine et al.Annual review of neuroscience (Print). 2010, Vol 33, pp 71-88, issn 0147-006X, 18 p.Article

Molecular Pathogenesis of Frontotemporal Lobar Degeneration : Basic Science Seminar in NeurologySLEEGERS, Kristel; KUMAR-SINGH, Samir; CRUTS, Marc et al.Archives of neurology (Chicago). 2008, Vol 65, Num 6, pp 700-704, issn 0003-9942, 5 p.Article

The pursuit of susceptibility genes for Alzheimer's disease: progress and prospectsSLEEGERS, Kristel; LAMBERT, Jean-Charles; BERTRAM, Lars et al.Trends in genetics (Regular ed.). 2010, Vol 26, Num 2, pp 84-93, issn 0168-9525, 10 p.Article

Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar DegenerationCHEN-PLOTKIN, Alice S; MARTINEZ-LAGE, Maria; WEINER, Myron F et al.Archives of neurology (Chicago). 2011, Vol 68, Num 4, pp 488-497, issn 0003-9942, 10 p.Article

Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementiaENGELBORGHS, Sebastiaan; DERMAUT, Bart; PICKUT, Barbara et al.Neurobiology of aging. 2006, Vol 27, Num 2, pp 285-292, issn 0197-4580, 8 p.Article

Linkage and association studies identify a novel locus for alzheimer disease at 7q36 in a dutch population-based sampleRADEMAKERS, Rosa; CRUTS, Marc; DE RIJK, Peter et al.American journal of human genetics. 2005, Vol 77, Num 4, pp 643-652, issn 0002-9297, 10 p.Article

Tau is central in the genetic Alzheimer-frontotemporal dementia spectrumDERMAUT, Bart; KUMAR-SINGH, Samir; RADEMAKERS, Rosa et al.Trends in genetics (Regular ed.). 2005, Vol 21, Num 12, pp 664-672, issn 0168-9525, 9 p.Article

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

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsyRADEMAKERS, Rosa; MELQUIST, Stacey; BEL KACEM, Samira et al.Human molecular genetics (Print). 2005, Vol 14, Num 21, pp 3281-3292, issn 0964-6906, 12 p.Article

Amyloid β secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's diseaseCRUTS, Marc; DERMAUT, Bart; RADEMAKERS, Rosa et al.Neuroscience letters. 2001, Vol 313, Num 1-2, pp 105-107, issn 0304-3940Article

Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP92)ROKS, Gerwin; VAN HARSKAMP, Frans; VAN SWIETEN, John C et al.Brain. 2000, Vol 123, pp 2130-2140, issn 0006-8950, 10Article

Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutationSINGLETON, Andrew B; HALL, Ros; DE JONGHE, Chris et al.Brain. 2000, Vol 123, pp 2467-2474, issn 0006-8950, 12Article

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

Cholesterol and triglycerides moderate the effect of apolipoprotein e on memory functioning in older adultsDE FRIAS, Cindy M; BUNCE, David; WAHLIN, Ake et al.The Journals of gerontology. Series B, Psychological sciences and social sciences. 2007, Vol 62, Num 2, issn 1079-5014, P112-P118Article

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

The influence of APOE status on episodic and semantic memory : Data from a population-based studyNILSSON, Lars-Göran; ADOLFSSON, Rolf; BÄCKMAN, Lars et al.Neuropsychology. 2006, Vol 20, Num 6, pp 645-657, issn 0894-4105, 13 p.Article

PRNP Val129 homozygosity increases risk for early-onset Alzheimer's diseaseDERMAUT, Bart; CROES, Esther A; RADEMAKERS, Rosa et al.Annals of neurology. 2003, Vol 53, Num 3, pp 409-412, issn 0364-5134, 4 p.Article

Systematic genetic study of Alzheimer disease in Latin America : Mutation frequencies of the amyloid β precursor protein and presenilin genes in ColombiaARANGO, Diana; CRUTS, Marc; JACQUIER, Martine et al.American journal of medical genetics. 2001, Vol 103, Num 2, pp 138-143, issn 0148-7299Article

Nonfibrillar diffuse amyloid deposition due to a γ₄₂-secretase site mutation points to an essential role for N-truncated Aβ₄₂in Alzheimer's diseaseKUMAR-SINGH, Samir; DE JONGHE, Chris; BACKHOVENS, Hubert et al.Human molecular genetics (Print). 2000, Vol 9, Num 18, pp 2589-2598, issn 0964-6906Article

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

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

Reduced hippocampal volume in non-demented carriers of the apolipoprotein E ε4 : Relation to chronological age and recognition memoryLIND, Johanna; LARSSON, Anne; NYBERG, Lars et al.Neuroscience letters. 2006, Vol 396, Num 1, pp 23-27, issn 0304-3940, 5 p.Article

Alzheimer-associated c allele of the promoter polymorphism -22C>T causes a critical neuron-specific decrease of presenilin 1 expressionTHEUNS, Jessie; REMACLE, Jacques; KILLICK, Richard et al.Human molecular genetics (Print). 2003, Vol 12, Num 8, pp 869-877, issn 0964-6906, 9 p.Article