Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p von Heinzlef, O, Paternotte, C, Mahieux, F, Prud'homme, J F, Dien, J, Madigand, M, Pouget, J, Weissenbach, J, Roullet, E, Hazan, J

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HLA profiles in multiple sclerosis suggest two forms of disease and the existence of protective haplotypes von Madigand, Michel, Oger, Joël J.-F., Fauchet, Renée, Sabouraud, Oliver, Genetet, Bernard

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Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia von Ducros, A., Denier, C., Joutel, A., Vahedi, K., Michel, A., Darcel, F., Madigand, M., Guerouaou, D., Tison, F., Julien, J., Hirsch, E., Chedru, F., Bisgård, C., Lucotte, G., Després, P., Billard, C., Barthez, M.A., Ponsot, G., Bousser, M.G., Tournier-Lasserve, E.

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