Search Results - Arne-Bes, M.C.

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  1. 1
    Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene

    Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene by Stojkovic, T, de Seze, J, Dubourg, O, Arne-Bes, M.C, Tardieu, S, Hache, J.C, Vermersch, P

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  2. 2
    G.P.281

    G.P.281 by Nectoux, J, de Cid, R, Baulande, S, Leturcq, F, Urtizberea, J.A, Penisson-Besnier, I, Nadaj Pakleza, A, Roudaut, C, Criqui, A, Orhant, L, Peyroulan, D, Yaou, R. Ben, Nelson, I, Arné-Bes, M.C, Nitschke, P, Claustres, M, Bonne, G, Lévy, N, Chelly, J, Richard, I, Cossée, M

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  3. 3
    Neuromyopathy secondary to Omeprazole treatment

    Neuromyopathy secondary to Omeprazole treatment by Faucheux, J.M., Tournebize, P., Viguier, A., Arne-Bes, M.C., Larrue, V., Géraud, G.

    Published in Muscle & nerve
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  4. 4
    Validation of an helicoidal versus standard ankle-foot orthosis for patients with unilateral drop foot

    Validation of an helicoidal versus standard ankle-foot orthosis for patients with unilateral drop foot by Gasq, D., Acket, B., Caussé, B., Cantagrel, N., Combe, E., Cintas, P., Arné-Bes, M.C.

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  5. 5
    WITHDRAWN: What is the place of electroneuromyographic studies in the diagnosis and management of pudendal neuralgia related to entrapment syndrome?

    WITHDRAWN: What is the place of electroneuromyographic studies in the diagnosis and management of pudendal neuralgia related to entrapment syndrome? by Lefaucheur, J.P., Labat, J.J., Amarenco, G., Herbaut, A.G., Prat-Pradal, D., Benaim, J., Aranda, B., Arne-Bes, M.C., Bonniaud, V., Boohs, P.M., Charvier, K., Daemgen, F., Dumas, P., Galaup, J.P., Ismael, S. Sheikh, Kerdraon, J., Lacroix, P., Lagauche, D., Lapeyre, E., Lefort, M., Leroi, A.M., Opsomer, R.J., Parratte, B., Prévinaire, J.G., Raibaut, P., Salle, J.Y., Scheiber-Nogueira, M.C., Soler, J.M., Testut, M.F., Thomas, C.

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  6. 6
    G.P.281: Detection of homozygous and compound heterozygous deletions in TRIM32 in LGMD patients analyzed by a combined strategy of CGH-array and Massive Parallel Sequencing

    G.P.281: Detection of homozygous and compound heterozygous deletions in TRIM32 in LGMD patients analyzed by a combined strategy of CGH-array and Massive Parallel Sequencing by Nectoux, J., de Cid, R., Baulande, S., Leturcq, F., Urtizberea, J.A., Penisson-Besnier, I., Nadaj Pakleza, A., Roudaut, C., Criqui, A., Orhant, L., Peyroulan, D., Yaou, R. Ben, Nelson, I., Arné-Bes, M.C., Nitschke, P., Claustres, M., Bonne, G., Lévy, N., Chelly, J., Richard, I., Cossée, M.

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  7. 7
    Les méfaits d’Internet dans les traitements de la sclérose latérale amyotrophique

    Les méfaits d’Internet dans les traitements de la sclérose latérale amyotrophique by Meininger, V., Antoine, J.-C., Arne-Bes, M.C., Broussolle, E., Bruneteau, G., Camdessanche, J.P., Camu, W., Carluer, L., Cintas, P., Clavelou, P., Corcia, P., Couratier, P., Danel-Brunaud, V., Desnuelle, C., Destée, A., Dib, M., Fleury, M.-C., Furby, A., Giroud, M., Gonzales, J., Guy, N., Kolev, I., Lacomblez, L., Lardillier-Noel, D., Le Forestier, N., Maugin, D., Nicolas, G., Pittion, S., Pouget, J., Pradat, P.F., Rousso, E., Salachas, F., Soriani, M.H., Tranchant, C., Vandenberghe, N., Verschueren, A., Viader, F., Vial, C.

    Published in Revue neurologique
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