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Results: 1-9 |
Results: 9
Association and excess of transmission of a DRD2 haplotype in a sample of French schizophrenic patients.
Authors: Dubertret, C Gorwood, P Gouya, L Deybach, JC Ades, J
Citation: C. Dubertret et al., Association and excess of transmission of a DRD2 haplotype in a sample of French schizophrenic patients., SCHIZOPHR R, 49(1-2), 2001, pp. 203-212
The genetics of addiction: alcohol-dependence and D3 dopamine receptor gene
Authors: Gorwood, P Limosin, F Batel, P Duaux, E Gouya, L Ades, J
Citation: P. Gorwood et al., The genetics of addiction: alcohol-dependence and D3 dopamine receptor gene, PATH BIOL, 49(9), 2001, pp. 710-717
New missense mutation in the human ferrochelatase gene in a family with erythropoietic protoporphyria: Functional studies and correlation of genotypeand phenotype
Authors: Rufenacht, UB Gregor, A Gouya, L Tarczynska-Nosal, L Schneider-Yin, X Deybach, JC
Citation: Ub. Rufenacht et al., New missense mutation in the human ferrochelatase gene in a family with erythropoietic protoporphyria: Functional studies and correlation of genotypeand phenotype, CLIN CHEM, 47(6), 2001, pp. 1112-1113
Reappraisal of the association between the DRD2 gene, alcoholism and addiction
Authors: Gorwood, P Batel, P Gouya, L Courtois, F Feingold, J Ades, J
Citation: P. Gorwood et al., Reappraisal of the association between the DRD2 gene, alcoholism and addiction, EUR PSYCHIA, 15(2), 2000, pp. 90-96
New insights into the pathogenesis of erythropoietic protoporphyria and their impact an patient care
Authors: Schneider-Yin, X Gouya, L Meier-Weinand, A Deybach, JC Minder, EI
Citation: X. Schneider-yin et al., New insights into the pathogenesis of erythropoietic protoporphyria and their impact an patient care, EUR J PED, 159(10), 2000, pp. 719-725
Mutations in the iron-sulfur cluster ligands of the human ferrochelatase lead to erythropoietic protoporphyria
Authors: Schneider-Yin, X Gouya, L Dorsey, M Rufenacht, U Deybach, JC Ferreira, GC
Citation: X. Schneider-yin et al., Mutations in the iron-sulfur cluster ligands of the human ferrochelatase lead to erythropoietic protoporphyria, BLOOD, 96(4), 2000, pp. 1545-1549
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update
Authors: Rosipal, R Lamoril, J Puy, H Da Silva, V Gouya, L De Rooij, FWM Te Velde, K Nordmann, Y Martasek, P Deybach, JC
Citation: R. Rosipal et al., Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update, HUM MUTAT, 13(1), 1999, pp. 44-53
Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresis
Authors: Tchernitchko, D Lamoril, J Puy, H Robreau, AM Bogard, C Rosipal, R Gouya, L Deybach, JC Nordmann, Y
Citation: D. Tchernitchko et al., Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresis, CLIN CHIM A, 279(1-2), 1999, pp. 133-143
Inheritance in erythropoietic protoporphyria: A common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestation
Authors: Gouya, L Puy, H Lamoril, J Da Silva, V Grandchamp, B Nordmann, Y Deybach, JC
Citation: L. Gouya et al., Inheritance in erythropoietic protoporphyria: A common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestation, BLOOD, 93(6), 1999, pp. 2105-2110
Risultati: 1-9 |