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The apolipoprotein E gene and its age-specific effects on cognitive function.
Liu F, Pardo LM, Schuur M, Sanchez-Juan P, Isaacs A, Sleegers K, de Koning I, Zorkoltseva IV, Axenovich TI, Witteman JC, Janssens AC, van Swieten JC, Aulchenko YS, Oostra BA, van Duijn CM. Liu F, et al. Among authors: de koning i. Neurobiol Aging. 2010 Oct;31(10):1831-3. doi: 10.1016/j.neurobiolaging.2008.09.015. Epub 2008 Nov 11. Neurobiol Aging. 2010. PMID: 19004527
Genetic risk factors for cerebral small-vessel disease in hypertensive patients from a genetically isolated population.
Schuur M, van Swieten JC, Schol-Gelok S, Ikram MA, Vernooij MW, Liu F, Isaacs A, de Boer R, de Koning I, Niessen WJ, Vrooman H, Oostra BA, van der Lugt A, Breteler MM, van Duijn CM. Schuur M, et al. Among authors: de boer r, de koning i. J Neurol Neurosurg Psychiatry. 2011 Jan;82(1):41-4. doi: 10.1136/jnnp.2009.176362. Epub 2010 Jul 28. J Neurol Neurosurg Psychiatry. 2011. PMID: 20667857
Insulin-resistance and metabolic syndrome are related to executive function in women in a large family-based study.
Schuur M, Henneman P, van Swieten JC, Zillikens MC, de Koning I, Janssens AC, Witteman JC, Aulchenko YS, Frants RR, Oostra BA, van Dijk KW, van Duijn CM. Schuur M, et al. Among authors: de koning i. Eur J Epidemiol. 2010 Aug;25(8):561-8. doi: 10.1007/s10654-010-9476-y. Epub 2010 Jun 29. Eur J Epidemiol. 2010. PMID: 20585974 Free PMC article.
Distinct genetic forms of frontotemporal dementia.
Seelaar H, Kamphorst W, Rosso SM, Azmani A, Masdjedi R, de Koning I, Maat-Kievit JA, Anar B, Donker Kaat L, Breedveld GJ, Dooijes D, Rozemuller JM, Bronner IF, Rizzu P, van Swieten JC. Seelaar H, et al. Among authors: de koning i. Neurology. 2008 Oct 14;71(16):1220-6. doi: 10.1212/01.wnl.0000319702.37497.72. Epub 2008 Aug 13. Neurology. 2008. PMID: 18703462
Brain perfusion patterns in familial frontotemporal lobar degeneration.
Seelaar H, Papma JM, Garraux G, de Koning I, Reijs AE, Valkema R, Rozemuller AJ, Salmon E, van Swieten JC. Seelaar H, et al. Among authors: de koning i. Neurology. 2011 Jul 26;77(4):384-92. doi: 10.1212/WNL.0b013e3182270456. Epub 2011 Jul 13. Neurology. 2011. PMID: 21753175
Phenotypic variation in hereditary frontotemporal dementia with tau mutations.
van Swieten JC, Stevens M, Rosso SM, Rizzu P, Joosse M, de Koning I, Kamphorst W, Ravid R, Spillantini MG, Niermeijer, Heutink P. van Swieten JC, et al. Among authors: de koning i. Ann Neurol. 1999 Oct;46(4):617-26. doi: 10.1002/1531-8249(199910)46:4<617::aid-ana10>3.0.co;2-i. Ann Neurol. 1999. PMID: 10514099
60 results