AAAAAA

   
Results: 1-9 |
Results: 9
APOE genotype: No influence on galantamine treatment efficacy nor on rate of decline in Alzheimer's disease
Authors: Aerssens, J Raeymaekers, P Lilienfeld, S Geerts, H Konings, F Parys, W
Citation: J. Aerssens et al., APOE genotype: No influence on galantamine treatment efficacy nor on rate of decline in Alzheimer's disease, DEMENT G C, 12(2), 2001, pp. 69-77
Linkage of mood disorders with D2, D3 and TH genes: a multicenter study
Authors: Serretti, A Macciardi, F Cusin, C Lattuada, E Souery, D Lipp, O Mahieu, B Van Broeckhoven, C Blackwood, D Muir, W Aschauer, HN Heiden, AM Ackenheil, M Fuchshuber, S Raeymaekers, P Verheyen, G Kaneva, R Jablensky, A Papadimitriou, GN Dikeos, DG Stefanis, CN Smeraldi, E Mendlewicz, J
Citation: A. Serretti et al., Linkage of mood disorders with D2, D3 and TH genes: a multicenter study, J AFFECT D, 58(1), 2000, pp. 51-61
A European multicenter association study of HTR2A receptor polymorphism inbipolar affective disorder
Authors: Massat, I Souery, D Lipp, O Blairy, S Papadimitriou, G Dikeos, D Ackenheil, M Fuchshuber, S Hilger, C Kaneva, R Milanova, V Verheyen, G Raeymaekers, P Staner, L Oruc, L Jakovljevic, M Serretti, A Macciardi, F Van Broeckhoven, C Mendlewicz, J
Citation: I. Massat et al., A European multicenter association study of HTR2A receptor polymorphism inbipolar affective disorder, AM J MED G, 96(2), 2000, pp. 136-140
Novel syndromic form of X-linked complicated spastic paraplegia
Authors: Claes, S Devriendt, K Van Goethem, G Roelen, L Meireleire, J Raeymaekers, P Cassiman, JJ Fryns, JP
Citation: S. Claes et al., Novel syndromic form of X-linked complicated spastic paraplegia, AM J MED G, 94(1), 2000, pp. 1-4
Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder
Authors: Verheyen, GR Villafuerte, SM Del-Favero, J Souery, D Mendlewicz, J Van Broeckhoven, C Raeymaekers, P
Citation: Gr. Verheyen et al., Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder, EUR J HUM G, 7(4), 1999, pp. 427-434
Tyrosine hydroxylase polymorphism and phenotypic heterogeneity in bipolar affective disorder: A multicenter association study
Authors: Souery, D Lipp, O Rivelli, SK Massat, I Serretti, A Cavallini, C Ackenheil, M Adolfsson, R Aschauer, H Blackwood, D Dam, H Dikeos, D Fuchshuber, S Heiden, M Jakovljevic, M Kaneva, R Kessing, L Lerer, B Lonnqvist, J Mellerup, T Milanova, V Muir, W Nylander, PO Oruc, L Papadimitriou, GN Pekkarinen, P Peltonen, L Pull, C Raeymaekers, P Shapira, B Smeraldi, E Staner, L Stefanis, C Verga, M Verheyen, G Macciardi, F Van Broeckhoven, C Mendlewicz, J
Citation: D. Souery et al., Tyrosine hydroxylase polymorphism and phenotypic heterogeneity in bipolar affective disorder: A multicenter association study, AM J MED G, 88(5), 1999, pp. 527-532
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11.23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1
Authors: Claes, S Volcke, P Devriendt, K Holvoet, M Raeymaekers, P Cassiman, JJ Fryns, JP
Citation: S. Claes et al., Regional localization of a gene for nonspecific XLMR to Xp11.3-p11.23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1, AM J MED G, 85(3), 1999, pp. 283-287
A new gene (DYX3) for dyslexia is located on chromosome 2
Authors: Fagerheim, T Raeymaekers, P Tonnessen, FE Pedersen, M Tranebjaerg, L Lubs, HA
Citation: T. Fagerheim et al., A new gene (DYX3) for dyslexia is located on chromosome 2, J MED GENET, 36(9), 1999, pp. 664-669
Homozygosity mapping to the USH2A locus in two isolated populations
Authors: Fagerheim, T Raeymaekers, P Merren, J Mani, K Jha, GK Baumbach, L Brox, V Breines, E Holdo, BE Holdo, A Tranebjaerg, L
Citation: T. Fagerheim et al., Homozygosity mapping to the USH2A locus in two isolated populations, J MED GENET, 36(2), 1999, pp. 144-147
Risultati: 1-9 |