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Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions.
Reus LM, Jansen IE, Mol MO, van Ruissen F, van Rooij J, van Schoor NM, Tesi N, Reinders MJT, Huisman MA, Holstege H, Visser PJ, de Boer SCM, Hulsman M, Ahmad S, Amin N, Uitterlinden AG, Ikram A, van Duijn CM, Seelaar H, Ramakers IHGB, Verhey FRJ, van der Lugt A, Claassen JAHR, Jan Biessels G, De Deyn PP, Scheltens P, van der Flier WM, van Swieten JC, Pijnenburg YAL, van der Lee SJ. Reus LM, et al. Among authors: van duijn cm, van ruissen f, van schoor nm, van swieten jc, van der flier wm, van der lee sj, van der lugt a, van rooij j. Transl Psychiatry. 2021 Sep 2;11(1):451. doi: 10.1038/s41398-021-01577-3. Transl Psychiatry. 2021. PMID: 34475377 Free PMC article.
Alcohol consumption and risk of dementia: the Rotterdam Study.
Ruitenberg A, van Swieten JC, Witteman JC, Mehta KM, van Duijn CM, Hofman A, Breteler MM. Ruitenberg A, et al. Among authors: van duijn cm, van swieten jc. Lancet. 2002 Jan 26;359(9303):281-6. doi: 10.1016/S0140-6736(02)07493-7. Lancet. 2002. PMID: 11830193
Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.
Rosso SM, Donker Kaat L, Baks T, Joosse M, de Koning I, Pijnenburg Y, de Jong D, Dooijes D, Kamphorst W, Ravid R, Niermeijer MF, Verheij F, Kremer HP, Scheltens P, van Duijn CM, Heutink P, van Swieten JC. Rosso SM, et al. Among authors: van duijn cm, van swieten jc. Brain. 2003 Sep;126(Pt 9):2016-22. doi: 10.1093/brain/awg204. Epub 2003 Jul 22. Brain. 2003. PMID: 12876142
A deletion in DJ-1 and the risk of dementia--a population-based survey.
Arias Vásquez A, Sleegers K, Dekker MC, van Gool WA, van Swieten JC, Aulchenko YS, Oostra BA, van Duijn CM. Arias Vásquez A, et al. Among authors: van duijn cm, van swieten jc, van gool wa. Neurosci Lett. 2004 Dec 6;372(3):196-9. doi: 10.1016/j.neulet.2004.09.040. Neurosci Lett. 2004. PMID: 15542239
Evidence for novel loci for late-onset Parkinson's disease in a genetic isolate from the Netherlands.
Bertoli-Avella AM, Dekker MC, Aulchenko YS, Houwing-Duistermaat JJ, Simons E, Testers L, Pardo LM, Rademaker TA, Snijders PJ, van Swieten JC, Bonifati V, Heutink P, van Duijn CM, Oostra BA. Bertoli-Avella AM, et al. Among authors: van duijn cm, van swieten jc. Hum Genet. 2006 Mar;119(1-2):51-60. doi: 10.1007/s00439-005-0108-7. Epub 2005 Dec 14. Hum Genet. 2006. PMID: 16369765
Progranulin mutations in Dutch familial frontotemporal lobar degeneration.
Bronner IF, Rizzu P, Seelaar H, van Mil SE, Anar B, Azmani A, Donker Kaat L, Rosso S, Heutink P, van Swieten JC. Bronner IF, et al. Among authors: van swieten jc, van mil se. Eur J Hum Genet. 2007 Mar;15(3):369-74. doi: 10.1038/sj.ejhg.5201772. Epub 2007 Jan 17. Eur J Hum Genet. 2007. PMID: 17228326
TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.
Seelaar H, Schelhaas HJ, Azmani A, Küsters B, Rosso S, Majoor-Krakauer D, de Rijk MC, Rizzu P, ten Brummelhuis M, van Doorn PA, Kamphorst W, Willemsen R, van Swieten JC. Seelaar H, et al. Among authors: van swieten jc, van doorn pa. Brain. 2007 May;130(Pt 5):1375-85. doi: 10.1093/brain/awm024. Epub 2007 Mar 14. Brain. 2007. PMID: 17360763 Free article.
376 results