Verpillat P - Search Results

1

Association of the Toll-like receptor 4 gene Asp299Gly polymorphism with acute coronary events.

Ameziane N, Beillat T, Verpillat P, Chollet-Martin S, Aumont MC, Seknadji P, Lamotte M, Lebret D, Ollivier V, de Prost D. Ameziane N, et al. Among authors: verpillat p. Arterioscler Thromb Vasc Biol. 2003 Dec;23(12):e61-4. doi: 10.1161/01.ATV.0000101191.92392.1D. Epub 2003 Oct 16. Arterioscler Thromb Vasc Biol. 2003. PMID: 14563652

2

Association of the -92C/G and 807C/T polymorphisms of the alpha2 subunit gene with human platelets alpha2beta1 receptor density.

Ajzenberg N, Berroeta C, Philip I, Grandchamp B, Ducellier P, Huart V, Verpillat P, Guillin MC, Benessiano J. Ajzenberg N, et al. Among authors: verpillat p. Arterioscler Thromb Vasc Biol. 2005 Aug;25(8):1756-60. doi: 10.1161/01.ATV.0000173308.13054.4f. Epub 2005 Jun 9. Arterioscler Thromb Vasc Biol. 2005. PMID: 15947241

3

Association study between iron-related genes polymorphisms and Parkinson's disease.

Borie C, Gasparini F, Verpillat P, Bonnet AM, Agid Y, Hetet G, Brice A, Dürr A, Grandchamp B; French Parkinson's disease genetic study group. Borie C, et al. Among authors: verpillat p. J Neurol. 2002 Jul;249(7):801-4. doi: 10.1007/s00415-002-0704-6. J Neurol. 2002. PMID: 12140659

4

Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensities.

Verpillat P, Alpérovitch A, Cambien F, Besançon V, Desal H, Tzourio C. Verpillat P, et al. Neurology. 2001 Mar 13;56(5):673-5. doi: 10.1212/wnl.56.5.673. Neurology. 2001. PMID: 11245725

5

Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis.

Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Lacomblez L, Moreaud O, Golfier V, Campion D, Brice A, Clerget-Darpoux F. Verpillat P, et al. Eur J Hum Genet. 2002 Jul;10(7):399-405. doi: 10.1038/sj.ejhg.5200820. Eur J Hum Genet. 2002. PMID: 12107813

6

Polymorphisms of insulin degrading enzyme gene are not associated with Alzheimer's disease.

Boussaha M, Hannequin D, Verpillat P, Brice A, Frebourg T, Campion D. Boussaha M, et al. Among authors: verpillat p. Neurosci Lett. 2002 Aug 23;329(1):121-3. doi: 10.1016/s0304-3940(02)00586-4. Neurosci Lett. 2002. PMID: 12161276

7

Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population.

Verpillat P, Bouley S, Campion D, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Antérion C, Agid Y, Brice A, Clerget-Darpoux F. Verpillat P, et al. Eur J Hum Genet. 2001 Jun;9(6):464-8. doi: 10.1038/sj.ejhg.5200644. Eur J Hum Genet. 2001. PMID: 11436129

8

Is the saitohin gene involved in neurodegenerative diseases?

Verpillat P, Ricard S, Hannequin D, Dubois B, Bou J, Camuzat A, Pradier L, Frebourg T, Brice A, Clerget-Darpoux F, Deleuze JF, Campion D; French Study Group on Alzheimer's Disease and Frontotemporal Dementia. Verpillat P, et al. Ann Neurol. 2002 Dec;52(6):829-32. doi: 10.1002/ana.10384. Ann Neurol. 2002. PMID: 12447938

9

Association between the extended tau haplotype and frontotemporal dementia.

Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Michel BF, Lacomblez L, Moreaud O, Sellal F, Golfier V, Campion D, Clerget-Darpoux F, Brice A. Verpillat P, et al. Arch Neurol. 2002 Jun;59(6):935-9. doi: 10.1001/archneur.59.6.935. Arch Neurol. 2002. PMID: 12056929

10

APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population.

Zurutuza L, Verpillat P, Raux G, Hannequin D, Puel M, Belliard S, Michon A, Pothin Y, Camuzat A, Penet C, Martin C, Brice A, Campion D, Clerget-Darpoux F, Frebourg T. Zurutuza L, et al. Among authors: verpillat p. Eur J Hum Genet. 2000 Sep;8(9):713-6. doi: 10.1038/sj.ejhg.5200513. Eur J Hum Genet. 2000. PMID: 10980578

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