Oostra BA - Search Results

1

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

2

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.

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

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

5

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.

6

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

7

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

8

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter.

Heutink P, van der Mey AG, Sandkuijl LA, van Gils AP, Bardoel A, Breedveld GJ, van Vliet M, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Among authors: oostra ba. Hum Mol Genet. 1992 Apr;1(1):7-10. doi: 10.1093/hmg/1.1.7. Hum Mol Genet. 1992. PMID: 1301144

9

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.

Heutink P, van de Wetering BJ, Breedveld GJ, Weber J, Sandkuyl LA, Devor EJ, Heiberg A, Niermeijer MF, Oostra BA. Heutink P, et al. Among authors: oostra ba. J Med Genet. 1990 Jul;27(7):433-6. doi: 10.1136/jmg.27.7.433. J Med Genet. 1990. PMID: 2395161 Free PMC article.

10

Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families.

Heutink P, van Schothorst EM, van der Mey AG, Bardoel A, Breedveld G, Pertijs J, Sandkuijl LA, van Ommen GJ, Cornelisse CJ, Oostra BA, et al. Heutink P, et al. Among authors: oostra ba. Eur J Hum Genet. 1994;2(3):148-58. doi: 10.1159/000472358. Eur J Hum Genet. 1994. PMID: 7834274

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