Heutink P - Search Results

1

A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarction.

Vaessen N, Heutink P, Janssen JA, Witteman JC, Testers L, Hofman A, Lamberts SW, Oostra BA, Pols HA, van Duijn CM. Vaessen N, et al. Among authors: heutink p. Diabetes. 2001 Mar;50(3):637-42. doi: 10.2337/diabetes.50.3.637. Diabetes. 2001. PMID: 11246885 Free article.

2

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: heutink p. 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.

3

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: heutink p. Mov Disord. 2001 Mar;16(2):290-3. doi: 10.1002/mds.1041. Mov Disord. 2001. PMID: 11295783 Clinical Trial.

4

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: heutink p. Neurology. 1997 Jun;48(6):1526-9. doi: 10.1212/wnl.48.6.1526. Neurology. 1997. PMID: 9191760

5

Mutation screening of the tau gene in patients with early-onset Alzheimer's disease.

Roks G, Dermaut B, Heutink P, Julliams A, Backhovens H, Van de Broeck M, Serneels S, Hofman A, Van Broeckhoven C, van Duijn CM, Cruts M. Roks G, et al. Among authors: heutink p. Neurosci Lett. 1999 Dec 24;277(2):137-9. doi: 10.1016/s0304-3940(99)00861-7. Neurosci Lett. 1999. PMID: 10624829

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: heutink p. 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: heutink p. Brain. 2004 Jul;127(Pt 7):1641-9. doi: 10.1093/brain/awh179. Epub 2004 May 6. Brain. 2004. PMID: 15130954

8

Dinucleotide repeat polymorphism at D11S994 locus.

Bontekoe CJ, de Graaff E, Breedveld GJ, Oostra BA, Heutink P. Bontekoe CJ, et al. Among authors: heutink p. Hum Mol Genet. 1993 Oct;2(10):1747. doi: 10.1093/hmg/2.10.1747. Hum Mol Genet. 1993. PMID: 8268942 No abstract available.

9

The genetic background of craniosynostosis syndromes.

Heutink P, Vermeij-Keers C, Oostra BA. Heutink P, et al. Eur J Hum Genet. 1995;3(5):312-23. doi: 10.1159/000472315. Eur J Hum Genet. 1995. PMID: 8556306 Review.

10

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: heutink p. Neurology. 1998 Jun;50(6):1541-5. doi: 10.1212/wnl.50.6.1541. Neurology. 1998. PMID: 9633692

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