Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: from stroke to vessel wall physiology

Por BOUSSER, M, TOURNIER-LASSERVE, E
Publicado em 2001

Spanish families with cavernous angiomas do not share the Hispano- American CCM1 haplotype

Por JUNG, H, LABAUGE, P, LABERGE, S, MARECHAL, E, TOURNIER-LASSERVE, E, LUCAS, M, GARCIA-MORENO, J, GAMERO, M, IZQUIERDO, G, TOURNIER-LASSERVE, E
Publicado em 1999

IL-2 receptor and HLA class II antigens on cerebrospinal fluid cells of patients with multiple sclerosis and other neurological diseases.

Por Tournier-Lasserve, E, Lyoncaen, O, Roullet, E, Bach, M A
Publicado em 1987

Prevalence of serum antibodies to hepatitis C virus is not increased in patients with multiple sclerosis.

Por Heinzlef, O, Roullet, E, Johanet, C, Tournier-Lasserve, E, Chazouilleres, O
Publicado em 1996

Remarkable intron and exon sequence conservation in human and mouse homeobox Hox 1.3 genes.

Por Tournier-Lasserve, E, Odenwald, W F, Garbern, J, Trojanowski, J, Lazzarini, R A
Publicado em 1989

Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical, familial, and biological characteristics

Por Heinzlef, O, Weill, B, Johanet, C, Sazdovitch, V, Caillat-Zucman, S, Tournier-Lasserve, E, Roullet, E
Publicado em 2002

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family.

Por Jung, H H, Bassetti, C, Tournier-Lasserve, E, Vahedi, K, Arnaboldi, M, Arifi, V B, Burgunder, J M
Publicado em 1995

Restricted T-cell receptor V beta gene usage by myelin basic protein-specific T-cell clones in multiple sclerosis: predominant genes vary in individuals.

Por Ben-Nun, A, Liblau, R S, Cohen, L, Lehmann, D, Tournier-Lasserve, E, Rosenzweig, A, Zhang, J W, Raus, J C, Bach, M A
Publicado em 1991

New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature.

Por Vérin, M, Rolland, Y, Landgraf, F, Chabriat, H, Bompais, B, Michel, A, Vahedi, K, Martinet, J P, Tournier-Lasserve, E, Lemaitre, M H
Publicado em 1995

Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q

Por Notelet, L, Chapon, F, Khoury, S, Vahedi, K, Chodkiewicz, J, Courtheoux, P, Iba-Zizen, M, Cabanis, E, Lechevalier, B, Tournier-Lasserve, E, Houtteville, J
Publicado em 1997

Genetic Heterogeneity of Familial Hemiplegic Migraine

Por Joutel, A., Ducros, A., Vahedi, K., Labauge, P., Delrieu, O., Pinsard, N., Mancini, J., Ponsot, G., Gouttière, F., Gastaut, J. L., Maziaceck, J., Weissenbach, J., Bousser, M. G., Tournier-Lasserve, E.
Publicado em 1994

CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas

Por Riant, F., Bergametti, F., Fournier, H.-D., Chapon, F., Michalak-Provost, S., Cecillon, M., Lejeune, P., Hosseini, H., Choe, C., Orth, M., Bernreuther, C., Boulday, G., Denier, C., Labauge, P., Tournier-Lasserve, E.
Publicado em 2013

Mutations within the Programmed Cell Death 10 Gene Cause Cerebral Cavernous Malformations

Por Bergametti, F., Denier, C., Labauge, P., Arnoult, M., Boetto, S., Clanet, M., Coubes, P., Echenne, B., Ibrahim, R., Irthum, B., Jacquet, G., Lonjon, M., Moreau, J. J., Neau, J. P., Parker, F., Tremoulet, M., Tournier-Lasserve, E.
Publicado em 2005

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Por 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
Publicado em 1999

Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations

Por Denier, C., Goutagny, S., Labauge, P., Krivosic, V., Arnoult, M, Cousin, A., Benabid, A. L., Comoy, J., Frerebeau, P., Gilbert, B., Houtteville, J. P., Jan, M., Lapierre, F., Loiseau, H., Menei, P., Mercier, P., Moreau, J. J., Nivelon-Chevallier, A., Parker, F., Redondo, A. M., Scarabin, J. M., Tremoulet, M., Zerah, M., Maciazek, J., Tournier-Lasserve, E.
Publicado em 2004

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Ieukoencephalopathy, Genetic Homogeneity, and Mapping of the Locus within a 2-cM Interval

Por Ducros, A., Nagy, T., Alamowitch, S., Nibbio, A., Joutel, A., Vahedi, K., Chabriat, H., Iba-Zizen, M. T., Julien, J., Davous, P., Goas, J. Y., Lyon-Caen, O., Dubois, B., Ducrocq, X., Salsa, F., Ragno, M., Burkhard, P., Bassetti, C., Hutchinson, M., Vérin, M., Viader, F., Chapon, F., Levasseur, M., Mas, J. L., Delrieu, O., Maciazek, J., Prieur, M., Mohrenweiser, H., Bach, J. F., Bousser, M. G., Tournier-Lasserve, E.
Publicado em 1996