Natalizumab and drug holiday in clinical practice: An observational study in very active relapsing remitting Multiple Sclerosis patients von Kerbrat, A, Le Page, E, Leray, E, Anani, T, Coustans, M, Desormeaux, C, Guiziou, C, Kassiotis, P, Lallement, F, Laplaud, D, Diraison, P, Rouhart, F, Sartori, E, Wardi, R, Wiertlewski, S, Edan, G

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Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene von Chapon, F, Latour, P, Diraison, P, Schaeffer, S, Vandenberghe, A

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Thrombolytic Therapy with Streptokinase in Acute Ischemic Stroke von Hommel, Marc, Cornu, C, Boutitie, F, Boissel, J P

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Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences : New tools for molecular diagnosis of hereditary neuropathy with liability to pressur... von LOPES, J, LEGUERN, E, GOUIDER, R, TARDIEU, S, ABBAS, N, BIROUK, N, GUGENHEIM, M, BOUCHE, P, AGID, Y, BRICE, A

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Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A von Chapon, F, Diraison, P, Lechevalier, B, Chazot, G, Viader, F, Bonnebouche, C, Vandenberghe, A, Timmerman, V, Van Broeckhoven, C

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Une diplopie récidivante révélatrice d’un lymphome orbitaire von Thomas, E., Lamotte, N., Breuilly, C., Hasle, D., Diraison, P., Coustans, M.

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Acute Necrotizing Vasculitis (Polyarteritis Nodosa?) Confined to the Nerve with Spontaneous Recovery von DE LA SAYETTE, V., MACRO, M., DIRAISON, PH, BERTRAN, F., LECHEVALIER, B., CHAPON, F.

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Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B von Latour, Philippe, Blanquet, Françoise, Nelis, Eva, Bonnebouche, Christine, Chapon, Fraņoise, Diraison, Philippe, Ollagnon, Elisabeth, Dautigny, André, Pham-Dinh, Danielle, Chazot, Guy, Boucherat, Michel, Van Broeckhoven, Christine, Vandenberghe, Antoon

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Charcot-Marie-Tooth type 1B neuropathy: A mutation at the single glycosylation site in the major peripheral myelin glycoprotein P0 von Blanquet-Grossard, Françoise, Pham-Dinh, Danielle, Dautigny, André, Latour, Philippe, Bonnebouche, Christine, Diraison, Philippe, Chapon, Françoise, Chazot, Guy, Vandenberghe, Antoon

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Marchiafava-Bignami disease. 3 cases with favorable prognosis von Diraison, P, Rouhart, F, Goas, P, Auclerc-Guichaoua, S, Gomes, C, Mocquard, Y, Goas, J Y

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Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po von Blanquet-Grossard, F, Pham-Dinh, D, Dautigny, A, Latour, P, Bonnebouche, C, Diraison, P, Chapon, F, Chazot, G, Vandenberghe, A

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Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases von LeGuern, E., Gouider, R., Lopes, J., Abbas, N., Gugenheim, M., Tardieu, S., Ravisé, N., Léger, J.-M., Vallat, J.-M., Bouche, P., Agid, Y., Brice, A., the French CMT Collaborative Research Group

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Encéphalite aiguë contemporaine d'une primo-invasion bilharzienne à Schistosoma mansoni von Graníer, H., Potard, M., Diraison, P., Nicolas, X., Laborde, J.P., Talarmin, F.

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La maladie de Marchiafava-Bignami. Trois observations d'évolution favorable von Diraison, P, Rouhart, F, Goas, P, Auclerc-Guichaoua, S, Gomes, C, Mocquard, Y, Goas, J.Y

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Encephalite aiguë contemporaine d'une primo-invasion Bilharzienne à Schistosoma mansoni von GRANIER, H, POTARD, M, DIRAISON, P, NICOLAS, X, LABORDE, J. P, TALARMIN, F

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Acute necrotizing vasculitis (polyarteritis nodosa?) confined to the nerve with spontaneous recovery von de la Sayette, V, Macro, M, Diraison, P, Bertran, F, Lechevalier, B, Chapon, F

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Acute necrotizing vasculitis (polyarteritis nodosa?) confined to the nerve with spontaneous recovery von de la Sayette, V, Macro, M, Diraison, P, Bertran, F, Lechevalier, B, Chapon, F

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The curved Magallanes fold and thrust belt: Tectonic insights from a paleomagnetic and anisotropy of magnetic susceptibility study von Poblete, F., Roperch, P., Hervé, F., Diraison, M., Espinoza, M., Arriagada, C.

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Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A von Chapon, F, Diraison, P, Lechevalier, B, Chazot, G, Viader, F, Bonnebouche, C, Vandenberghe, A, Timmerman, V, Van Broeckhoven, C

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Contribution of hepatic de novo lipogenesis and reesterification of plasma non esterified fatty acids to plasma triglyceride synthesis during non-alcoholic fatty liver disease von Diraison, F, Moulin, Ph, Beylot, M

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