Oostra BA - Search Results

1

Familial aggregation in frontotemporal dementia.

Stevens M, van Duijn CM, Kamphorst W, de Knijff P, Heutink P, van Gool WA, Scheltens P, Ravid R, Oostra BA, Niermeijer MF, van Swieten JC. Stevens M, et al. Among authors: oostra ba. Neurology. 1998 Jun;50(6):1541-5. doi: 10.1212/wnl.50.6.1541. Neurology. 1998. PMID: 9633692

2

Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families.

Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, van Duijn CM, Oostra BA, van Swieten JC. Heutink P, et al. Among authors: oostra ba. Ann Neurol. 1997 Feb;41(2):150-9. doi: 10.1002/ana.410410205. Ann Neurol. 1997. PMID: 9029063

3

Apolipoprotein E gene and sporadic frontal lobe dementia.

Stevens M, van Duijn CM, de Knijff P, van Broeckhoven C, Heutink P, Oostra BA, Niermeijer MF, van Swieten JC. Stevens M, et al. Among authors: oostra ba. Neurology. 1997 Jun;48(6):1526-9. doi: 10.1212/wnl.48.6.1526. Neurology. 1997. PMID: 9191760

4

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.

Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, van Duijn CM, Heutink P. Rizzu P, et al. Among authors: oostra ba. Am J Hum Genet. 1999 Feb;64(2):414-21. doi: 10.1086/302256. Am J Hum Genet. 1999. PMID: 9973279 Free PMC article.

5

A clinical-genetic study of Parkinson's disease in a genetically isolated community.

Dekker MC, van Swieten JC, Houwing-Duistermaat JJ, Snijders PJ, Boeren E, Hofman A, Breteler MM, Heutink P, Oostra BA, van Duijn CM. Dekker MC, et al. Among authors: oostra ba. J Neurol. 2003 Sep;250(9):1056-62. doi: 10.1007/s00415-003-0151-z. J Neurol. 2003. PMID: 14504966

6

Familial clustering and genetic risk for dementia in a genetically isolated Dutch population.

Sleegers K, Roks G, Theuns J, Aulchenko YS, Rademakers R, Cruts M, van Gool WA, Van Broeckhoven C, Heutink P, Oostra BA, van Swieten JC, van Duijn CM. Sleegers K, et al. Among authors: oostra ba. Brain. 2004 Jul;127(Pt 7):1641-9. doi: 10.1093/brain/awh179. Epub 2004 May 6. Brain. 2004. PMID: 15130954

7

Familial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated population.

van Rijn MJ, Slooter AJ, Schut AF, Isaacs A, Aulchenko YS, Snijders PJ, Kappelle LJ, van Swieten JC, Oostra BA, van Duijn CM. van Rijn MJ, et al. Among authors: oostra ba. Neurology. 2005 Oct 25;65(8):1203-9. doi: 10.1212/01.wnl.0000178744.42953.b7. Epub 2005 Sep 14. Neurology. 2005. PMID: 16162858

8

N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam study.

Harhangi BS, Oostra BA, Heutink P, van Duijn CM, Hofman A, Breteler MM. Harhangi BS, et al. Among authors: oostra ba. J Neurol Neurosurg Psychiatry. 1999 Oct;67(4):518-20. doi: 10.1136/jnnp.67.4.518. J Neurol Neurosurg Psychiatry. 1999. PMID: 10486401 Free PMC article.

9

Genetic study on Tourette syndrome in The Netherlands.

Heutink P, van de Wetering BJ, Breedveld GJ, Oostra BA. Heutink P, et al. Among authors: oostra ba. Adv Neurol. 1992;58:167-72. Adv Neurol. 1992. PMID: 1414621 Review. No abstract available.

10

CYP2D6 polymorphism in Parkinson's disease: the Rotterdam Study.

Harhangi BS, Oostra BA, Heutink P, van Duijn CM, Hofman A, Breteler MM. Harhangi BS, et al. Among authors: oostra ba. Mov Disord. 2001 Mar;16(2):290-3. doi: 10.1002/mds.1041. Mov Disord. 2001. PMID: 11295783 Clinical Trial.

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