Verpillat P - Search Results

1

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

2

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

3

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

4

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

5

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

Dumanchin C, Camuzat A, Campion D, Verpillat P, Hannequin D, Dubois B, Saugier-Veber P, Martin C, Penet C, Charbonnier F, Agid Y, Frebourg T, Brice A. Dumanchin C, et al. Among authors: verpillat p. Hum Mol Genet. 1998 Oct;7(11):1825-9. doi: 10.1093/hmg/7.11.1825. Hum Mol Genet. 1998. PMID: 9736786

6

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

7

Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.

Lücking CB, Chesneau V, Lohmann E, Verpillat P, Dulac C, Bonnet AM, Gasparini F, Agid Y, Dürr A, Brice A. Lücking CB, et al. Among authors: verpillat p. Arch Neurol. 2003 Sep;60(9):1253-6. doi: 10.1001/archneur.60.9.1253. Arch Neurol. 2003. PMID: 12975291

8

Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation.

Raux G, Gantier R, Thomas-Anterion C, Boulliat J, Verpillat P, Hannequin D, Brice A, Frebourg T, Campion D. Raux G, et al. Among authors: verpillat p. Neurology. 2000 Nov 28;55(10):1577-8. doi: 10.1212/wnl.55.10.1577. Neurology. 2000. PMID: 11094121

9

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.

Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A; French Research Network on FTD/FTD-MND. Le Ber I, et al. Among authors: verpillat p. Neurology. 2009 May 12;72(19):1669-76. doi: 10.1212/WNL.0b013e3181a55f1c. Neurology. 2009. PMID: 19433740

10

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

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