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Results: 1-6 |
Results: 6

Authors: Dubourg, O Tardieu, S Birouk, N Gouider, R Leger, JM Maisonobe, T Brice, A Bouche, P LeGuern, E
Citation: O. Dubourg et al., The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity, NEUROMUSC D, 11(5), 2001, pp. 458-463

Authors: Dubourg, O Tardieu, S Birouk, N Gouider, R Leger, JM Maisonobe, T Brice, A Bouche, P LeGuern, E
Citation: O. Dubourg et al., Clinical, electrophysiological and molecular genetic characteristics of 93patients with X-linked Charcot-Marie-Tooth disease, BRAIN, 124, 2001, pp. 1958-1967

Authors: Fredj, M Mrad, FEB Karoui, M Ben Mrad, S Gouider, R Mrabet, A
Citation: M. Fredj et al., Rendu-Osler disease and epilepsy, REV NEUROL, 156(8-9), 2000, pp. 794-795

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: Gouider, R Samet, S Triki, C Fredj, M Gargouri, A El Bahri, F Ben Ghorbel, I Kasraoui, A Mhiri, C Mrabet, A
Citation: R. Gouider et al., Neurological manifestations revealing brucellosis., REV NEUROL, 155(3), 1999, pp. 215-218

Authors: Mouton, P Tardieu, S Gouider, R Birouk, N Maisonabe, T Dubourg, O Brice, A LeGuern, E Bouche, P
Citation: P. Mouton et al., Spectrum of clinical and electrophysiologic features in HNPP patients withthe 17p11.2 deletion, NEUROLOGY, 52(7), 1999, pp. 1440-1446
Risultati: 1-6 |