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

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

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

Guanosine Triphosphate Cyclohydrolase 1 Promoter Deletion Causes Dopa-Responsive DystoniaTHEUNS, Jessie; CROSIERS, David; MATTHEIJSSENS, Maria et al.Movement disorders. 2012, Vol 27, Num 11, pp 1451-1456, issn 0885-3185, 6 p.Article

GIGYF2 has no major role in Parkinson genetic etiology in a Belgian populationMEEUS, Bram; NUYTEMANS, Karen; DE DEYN, Peter Paul et al.Neurobiology of aging. 2011, Vol 32, Num 2, pp 308-312, issn 0197-4580, 5 p.Article

A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaquesDERMAUT, Bart; KUMAR-SINGH, Samir; CLAES, Stephen et al.Annals of neurology. 2004, Vol 55, Num 5, pp 617-626, issn 0364-5134, 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

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

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patientsNUYTEMANS, Karen; RADEMAKERS, Rosa; CRAS, Patrick et al.European journal of human genetics. 2008, Vol 16, Num 4, pp 471-479, issn 1018-4813, 9 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