Ben-Nun, A, Liblau, R S, Cohen, L, Lehmann, D, Tournier-Lasserve, E, Rosenzweig, A, ...
Recent studies in experimental autoimmune encephalomyelitis as a model for multiple sclerosis (MS) have demonstrated limited heterogeneity in T-cell antigen receptors (TCR) specific for myelin basic...
Remarkable intron and exon sequence conservation in human and mouse homeobox Hox 1.3 genes.
Tournier-Lasserve, E, Odenwald, W F, Garbern, J, Trojanowski, J, Lazzarini, R A
A high degree of conservation exists between the Hox 1.3 homeobox genes of mice and humans. The two genes occupy the same relative positions in their respective Hox 1 gene clusters, they show...
Ducros, A, Denier, C, Joutel, A, Vahedi, K, Michel, A, Darcel, F, ...
Familial hemiplegic migraine (HM) is an autosomal dominant migraine with aura. In 20% of HM families, HM is associated with a mild permanent cerebellar ataxia (PCA). The CACNA1A gene encoding the...
Ben-Nun, A, Liblau, R S, Cohen, L, Lehmann, D, Tournier-Lasserve, E, Rosenzweig, A, ...
Recent studies in experimental autoimmune encephalomyelitis as a model for multiple sclerosis (MS) have demonstrated limited heterogeneity in T-cell antigen receptors (TCR) specific for myelin basic...
Remarkable intron and exon sequence conservation in human and mouse homeobox Hox 1.3 genes.
Tournier-Lasserve, E, Odenwald, W F, Garbern, J, Trojanowski, J, Lazzarini, R A
A high degree of conservation exists between the Hox 1.3 homeobox genes of mice and humans. The two genes occupy the same relative positions in their respective Hox 1 gene clusters, they show...
Mutations within the MGC4607 Gene Cause Cerebral Cavernous Malformations
Denier, C., Goutagny, S., Labauge, P., Krivosic, V., Arnoult, M, Cousin, A., ...
Cerebral cavernous malformations (CCM) are hamartomatous vascular malformations characterized by abnormally enlarged capillary cavities without intervening brain parenchyma. They cause seizures and...
Mutations within the Programmed Cell Death 10 Gene Cause Cerebral Cavernous Malformations
Bergametti, F., Denier, C., Labauge, P., Arnoult, M., Boetto, S., Clanet, M., ...
Cerebral cavernous malformations (CCMs) are hamartomatous vascular malformations characterized by abnormally enlarged capillary cavities without intervening brain parenchyma. They cause seizures and...
Ducros, A, Denier, C, Joutel, A, Vahedi, K, Michel, A, Darcel, F, ...
Familial hemiplegic migraine (HM) is an autosomal dominant migraine with aura. In 20% of HM families, HM is associated with a mild permanent cerebellar ataxia (PCA). The CACNA1A gene encoding the...
Tournier-Lasserve, E, Lyoncaen, O, Roullet, E, Bach, M A
The presence of IL-2 receptor and HLA class II antigens as detected by monoclonal antibodies on mononuclear cells from both cerebro-spinal fluid (CSF) and peripheral blood was examined by...
Ducros, A., Nagy, T., Alamowitch, S., Nibbio, A., Joutel, A., Vahedi, K., ...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a recently identified autosomal dominant cerebral arteriopathy characterized by the recurrence...
Genetic Heterogeneity of Familial Hemiplegic Migraine
Joutel, A., Ducros, A., Vahedi, K., Labauge, P., Delrieu, O., Pinsard, N., ...
Familial hemiplegic migraine (FHM) is an autosomal dominant variety of migraine with aura. We previously mapped a gene responsible for this disorder to the short arm of chromosome 19, within a 30-cM...
Jung, H H, Bassetti, C, Tournier-Lasserve, E, Vahedi, K, Arnaboldi, M, Arifi, V B, ...
This paper reports a Swiss family affected by a cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) linked to chromosome 19q12. In three generations...
Vérin, M, Rolland, Y, Landgraf, F, Chabriat, H, Bompais, B, Michel, A, ...
A survey was carried out on a large family presenting the symptoms of familial arteriopathy (CADASIL) recently mapped to chromosome 19. This is characterised clinically by recurrent subcortical...
Spanish families with cavernous angiomas do not share the Hispano- American CCM1 haplotype
JUNG, H, LABAUGE, P, LABERGE, S, MARECHAL, E, TOURNIER-LASSERVE, E, LUCAS, M, ...
Heinzlef, O, Weill, B, Johanet, C, Sazdovitch, V, Caillat-Zucman, S, Tournier-Lasserve, E, ...
Objectives: To determine whether patients with MS who are positive for aCL Ab have specific characteristics.
Notelet, L, Chapon, F, Khoury, S, Vahedi, K, Chodkiewicz, J, Courtheoux, P, ...
OBJECTIVES—To characterise clinically a large French family affected with cerebral cavernomas and to check for linkage of this condition to chromosome 7. METHODS—A family, originating from...