AAAAAA

   
Results: 1-6 |
Results: 6

Authors: Baulac, S An-Gourfinkel, I Prud'homme, JF Baulac, M Bruzzone, R Brice, A Le Guern, E
Citation: S. Baulac et al., First genetic evidence of GABA(A) receptor dysfunction in epilepsy, M S-MED SCI, 17(8-9), 2001, pp. 908-909

Authors: Baulac, S An, I Brice, A Le Guern, E
Citation: S. Baulac et al., Epilepsy, febrile seizures and ion channels, M S-MED SCI, 17(10), 2001, pp. 999-1007

Authors: Pingault, V Bondurand, N Le Caignec, C Tardieu, S Lemort, N Dubourg, O Le Guern, E Goossens, M Boespflug-Tanguy, O
Citation: V. Pingault et al., The SOX10 transcription factor: evaluation as a candidate gene for centraland peripheral hereditary myelin disorders, J NEUROL, 248(6), 2001, pp. 496-499

Authors: Zemmouri, R Azzedine, H Assami, S Kitouni, N Vallat, JM Maisonobe, T Hamadouche, T Kessaci, M Mansouri, B Le Guern, E Grid, D Tazir, M
Citation: R. Zemmouri et al., Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathy, NEUROMUSC D, 10(8), 2000, pp. 592-598

Authors: Bouche, P Mouton, P Gouider, R Dubourg, O Le Guern, E Maisonobe, T le Forestier, N
Citation: P. Bouche et al., Hereditary neuropathy by pressure hypersensitivity, REV NEUROL, 156(10), 2000, pp. 915-919

Authors: Delmotte, C Le Guern, E Trudelle, Y Delmas, A
Citation: C. Delmotte et al., Structural features of a chimeric peptide inducing cytotoxic T lymphocyte responses in saline, EUR J BIOCH, 265(1), 1999, pp. 336-345
Risultati: 1-6 |