Genetics of familial ALS and consequences for diagnosis von Camu, W, Khoris, J, Moulard, B, Salachas, F, Briolotti, V, Rouleau, G.A, Meininger, V

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Mutations of SCN1A , encoding a neuronal sodium channel, in two families with GEFS+2 von Meisler, Miriam H, Brice, Alexis, Escayg, Andrew, Baulac, Stéphanie, Chaigne, Denys, An-Gourfinkel, Isabelle, Huberfeld, Gilles, LeGuern, Eric, Moulard, Bruno, Malafosse, Alain, MacDonald, Bryan T, Buresi, Catherine

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Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME von Moore, Tom, Hecquet, Stéphane, McLellann, Andrew, Ville, Dorothée, Grid, Djamel, Picard, Fabienne, Moulard, Bruno, Asherson, Philip, Makoff, Andrew J, McCormick, David, Nashef, Lina, Froguel, Philippe, Arzimanoglou, Alexis, LeGuern, Eric, Bailleul, Bernard

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Vascular Factors and Risk of Dementia: Design of the Three-City Study and Baseline Characteristics of the Study Population von 3C Study Group

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Epilepsy and sodium channel blockers von Moulard, B, Bertrand, D

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Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country von Khoris, J., Moulard, B., Briolotti, V., Hayer, M., Durieux, A., Clavelou, P., Malafosse, A., Rouleau, G. A., Camu, W.

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Identification of a New Locus for Generalized Epilepsy with Febrile Seizures Plus (GEFS+) on Chromosome 2q24-q33 von Moulard, Bruno, Chaigne, Denys, Mouthon, Dominique, Buresi, Catherine, Guipponi, Michel, Malafosse, Alain

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A nonsense mutation in the α4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI) von Beck, C., Moulard, B., Steinlein, O., Guipponi, M., Vallee, L., Montpied, P., Baldy-Moulnier, M., Malafosse, A.

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GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsy von Salzmann, Annick, Moulard, Bruno, Crespel, Arielle, Baldy-Moulinier, Michel, Buresi, Catherine, Malafosse, Alain

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Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease von Moulard, Bruno, Salachas, Francois, Chassande, Bénédicte, Briolotti, Valerie, Meininger, Vincent, Malafosse, Alain, Camu, William

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Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosis von Moulard, Bruno, Sefiani, Abdelaziz, Laamri, Aboubakr, Malafosse, Alain, Camu, William

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Study of the voltage-gated sodium channel beta 1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC) von Moulard, B, Buresi, C, Malafosse, A

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Founder Effect in Patients with Unverricht‐Lundborg Disease on Reunion Island von Moulard, Bruno, Darcel, Françoise, Mignard, Didier, Jeanpierre, Marc, Genton, Pierre, Cartault, François, Yaouanq, Jacqueline, Roubertie, Agathe, Biraben, Arnaud, Buresi, Catherine, Malafosse, Alain

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Ion channel variation causes epilepsies von Moulard, Bruno, Picard, Fabienne, le Hellard, Stéphanie, Agulhon, Cendra, Weiland, Sigrid, Favre, Isabelle, Bertrand, Sonia, Malafosse, Alain, Bertrand, Daniel

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Clinical heterogeneity in pedigrees with 2q-linked febrile seizures von Moulard, Bruno, Chaigne, Denys, Malafosse, Alain

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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations von MOULARD, Bruno, GENTON, Pierre, UTERMANN, Barbara, BALDY-MOULINIER, Michel, BELAIDI, Halima, BERTRAN, Francoise, BIRABEN, Arnaud, CHERIF, André Ali, CHKILI, Taieb, CRESPEL, Arielle, DARCEL, Francoise, DULAC, Olivier, GRID, Djamel, GENY, Christian, HUMBERT-CLAUDE, Véronique, KASSIOTIS, Philippe, BURESI, Catherine, MALAFOSSE, Alain, JEANPIERRE, Marc, OUAZZANI, Réda, MRABET, Amel, MORRIS, Mike, LEGUEM, Eric, DRAVET, Charlotte, MAUGUIERE, Francois

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Genetics of familial ALS and consequences for diagnosis. French ALS Research Group von Camu, W, Khoris, J, Moulard, B, Salachas, F, Briolotti, V, Rouleau, G A, Meininger, V

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169 Generalized epilepsy and febrile seizures plus syndrome: Linkage to chromosome 2q von Moulard, B., Guipponi, M., Chaigne, D., Mouthon, D., Buresi, C., Malafosse, A.

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A nonsense mutation in the alpha4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI) von Beck, C, Moulard, B, Steinlein, O, Guipponi, M, Vallee, L, Montpied, P, Baldy-Moulnier, M, Malafosse, A

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Clinical heterogeneity in pedigrees with 2q-linked febrile seizures von Moulard, B, Chaigne, D, Malafosse, A

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