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Page 1
Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease.
Martinez M, Campion D, Brice A, Hannequin D, Dubois B, Didierjean O, Michon A, Thomas-Anterion C, Puel M, Frebourg T, Agid Y, Clerget-Darpoux F. Martinez M, et al. Among authors: frebourg t. Arch Neurol. 1998 Jun;55(6):810-6. doi: 10.1001/archneur.55.6.810. Arch Neurol. 1998. PMID: 9626772
[Genetics of Alzheimer's disease].
Hannequin D, Campion D, Brice A, Frebourg T, Martinez M, Clerget-Darpoux F, Agid Y. Hannequin D, et al. Among authors: frebourg t. Rev Med Interne. 1996;17(7):545-50. doi: 10.1016/0248-8663(96)83090-6. Rev Med Interne. 1996. PMID: 8881379 Review. French.
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.
Bickeböller H, Campion D, Brice A, Amouyel P, Hannequin D, Didierjean O, Penet C, Martin C, Pérez-Tur J, Michon A, Dubois B, Ledoze F, Thomas-Anterion C, Pasquier F, Puel M, Demonet JF, Moreaud O, Babron MC, Meulien D, Guez D, Chartier-Harlin MC, Frebourg T, Agid Y, Martinez M, Clerget-Darpoux F. Bickeböller H, et al. Among authors: frebourg t. Am J Hum Genet. 1997 Feb;60(2):439-46. Am J Hum Genet. 1997. PMID: 9012418 Free PMC article.
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease.
Didierjean O, Martinez M, Campion D, Hannequin D, Dubois B, Martin C, Puel M, Thomas Anterion C, Pasquier F, Moreau O, Babron MC, Penet C, Agid Y, Clerget-Darpoux F, Frebourg T, Brice A. Didierjean O, et al. Among authors: frebourg t. J Neurol Neurosurg Psychiatry. 1997 Jul;63(1):103-5. doi: 10.1136/jnnp.63.1.103. J Neurol Neurosurg Psychiatry. 1997. PMID: 9221977 Free PMC article.
Association study of the GAB2 gene with the risk of developing Alzheimer's disease.
Chapuis J, Hannequin D, Pasquier F, Bentham P, Brice A, Leber I, Frebourg T, Deleuze JF, Cousin E, Thaker U, Amouyel P, Mann D, Lendon C, Campion D, Lambert JC. Chapuis J, et al. Among authors: frebourg t. Neurobiol Dis. 2008 Apr;30(1):103-6. doi: 10.1016/j.nbd.2007.12.006. Epub 2008 Jan 5. Neurobiol Dis. 2008. PMID: 18272374
ABCA7 rare variants and Alzheimer disease risk.
Le Guennec K, Nicolas G, Quenez O, Charbonnier C, Wallon D, Bellenguez C, Grenier-Boley B, Rousseau S, Richard AC, Rovelet-Lecrux A, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, Deleuze JF, Amouyel P, Munter HM, Bourque G, Lathrop M, Frebourg T, Redon R, Letenneur L, Dartigues JF, Pasquier F, Rollin-Sillaire A, Génin E, Lambert JC, Hannequin D, Campion D; CNR-MAJ collaborators. Le Guennec K, et al. Among authors: frebourg t. Neurology. 2016 Jun 7;86(23):2134-7. doi: 10.1212/WNL.0000000000002627. Epub 2016 Apr 1. Neurology. 2016. PMID: 27037229 Free PMC article.
No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.
Campion D, Brice A, Hannequin D, Charbonnier F, Dubois B, Martin C, Michon A, Penet C, Bellis M, Calenda A, Martinez M, Agid Y, Clerget-Darpoux F, Frebourg T. Campion D, et al. Among authors: frebourg t. J Med Genet. 1996 Aug;33(8):661-4. doi: 10.1136/jmg.33.8.661. J Med Genet. 1996. PMID: 8863158 Free PMC article.
401 results