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Results: 1-7 |
Results: 7
IGHV3-associated restriction fragment length polymorphisms confer susceptibility to bullous pemphigoid
Authors: Raux, G Gilbert, D Joly, P Martel, P Roujeau, JC Prost, C Lefranc, MP Tron, F
Citation: G. Raux et al., IGHV3-associated restriction fragment length polymorphisms confer susceptibility to bullous pemphigoid, EXP CLIN IM, 18(2), 2001, pp. 59-66
APOE promoter polymorphisms do not confer independent risk for Alzheimer'sdisease in a French population
Authors: 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
Citation: L. Zurutuza et al., APOE promoter polymorphisms do not confer independent risk for Alzheimer'sdisease in a French population, EUR J HUM G, 8(9), 2000, pp. 713-716
Association of KM genotype with bullous pemphigoid
Authors: Raux, G Gilbert, D Joly, P Daveau, M Martel, P Christ, M Tron, F
Citation: G. Raux et al., Association of KM genotype with bullous pemphigoid, J AUTOIMMUN, 14(1), 2000, pp. 79-82
Mutations in the neuroserpin gene are rare in familial dementia
Authors: Camuzat, A Verpillat, P Dubois, B Penet, C Agid, CPY Brice, A Clerget-Darpoux, F Moreaud, O Puel, M Kinter, J Kozlov, S Berger, P Sonderegger, P Raux, G Campion, D Hannequin, D Frebourg, T
Citation: A. Camuzat et al., Mutations in the neuroserpin gene are rare in familial dementia, ANN NEUROL, 47(5), 2000, pp. 688-688
Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation
Authors: Raux, G Gantier, R Thomas-Anterion, C Boulliat, J Verpillat, P Hannequin, D Brice, A Frebourg, T Campion, D
Citation: G. Raux et al., Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation, NEUROLOGY, 55(10), 2000, pp. 1577-1578
Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments
Authors: Charbonnier, F Raux, G Wang, Q Drouot, N Cordier, F Limacber, JM Saurin, JC Puisieux, A Olschwang, S Frebourg, T
Citation: F. Charbonnier et al., Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments, CANCER RES, 60(11), 2000, pp. 2760-2763
Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum
Authors: Campion, D Dumanchin, C Hannequin, D Dubois, B Belliard, S Puel, M Thomas-Anterion, C Michon, A Martin, C Charbonnier, F Raux, G Camuzat, A Penet, C Mesnage, V Martinez, M Clerget-Darpoux, F Brice, A Frebourg, T
Citation: D. Campion et al., Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum, AM J HU GEN, 65(3), 1999, pp. 664-670
Risultati: 1-7 |