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收藏KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects
Bowerman, Melissa; Salsac, Celine; Bernard, Veronique; Soulard, Claire; Dionne, Annie; Coque, Emmanuelle; Benlefki, Salim; Hince, Pascale; Dion, Patrick A.; Butler-Browne, Gillian; Camu, William; Bouchard, Jean-Pierre; Delpire, Eric; Rouleau, Guy A.; Raoul, Cedric; Scamps, Frederique
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收藏Long-term safety and efficacy of teriflunomide Nine-year follow-up of the randomized TEMSO study
O'Connor, Paul; Comi, Giancarlo; Freedman, Mark S.; Miller, Aaron E.; Kappos, Ludwig; Bouchard, Jean-Pierre; Lebrun-Frenay, Christine; Mares, Jan; Benamor, Myriam; Thangavelu, Karthinathan; Liang, Jinjun; Truffinet, Philippe; Lawson, Victoria J.; Wolinsky, Jerry S.
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收藏Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis
Leblond, Claire S.; Gan-Or, Ziv; Spiegelman, Dan; Laurent, Sandra B.; Szuto, Anna; Hodgkinson, Alan; Dionne-Laporte, Alexandre; Provencher, Pierre; de Carvalho, Mamede; Orru, Sandro; Brunet, Denis; Bouchard, Jean-Pierre; Awadalla, Philip; Dupre, Nicolas; Dion, Patrick A.; Rouleau, Guy A.
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收藏SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases
Choquet, Karine; Tetreault, Martine; Yang, Sharon; La Piana, Roberta; Dicaire, Marie-Josee; Vanstone, Megan R.; Mathieu, Jean; Bouchard, Jean-Pierre; Rioux, Marie-France; Rouleau, Guy A.; Boycott, Kym M.; Majewski, Jacek; Brais, Bernard
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收藏Early detection of structural abnormalities and cytoplasmic accumulation of TDP-43 in tissue-engineered skins derived from ALS patients
Pare, Bastien; Touzel-Deschenes, Lydia; Lamontagne, Remy; Lamarre, Marie-Soleil; Scott, Francois-Dominique; Khuong, Helene T.; Dion, Patrick A.; Bouchard, Jean-Pierre; Gould, Peter; Rouleau, Guy A.; Dupre, Nicolas; Berthod, Francois; Gros-Louis, Francois
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收藏Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele-Specific Expression
Giorgio, Elisa; Rolyan, Harshvardhan; Kropp, Laura; Chakka, Anish Baswanth; Yatsenko, Svetlana; Di Gregorio, Eleonora; Lacerenza, Daniela; Vaula, Giovanna; Talarico, Flavia; Mandich, Paola; Toro, Camilo; Pierre, Eleonore Eymard; Labauge, Pierre; Capellari, Sabina; Cortelli, Pietro; Vairo, Filippo Pinto; Miguel, Diego; Stubbolo, Danielle; Marques, Lourenco Charles; Gahl, William; Boespflug-Tanguy, Odile; Melberg, Atle; Hassin-Baer, Sharon; Cohen, Oren S.; Pjontek, Rastislav; Grau, Armin; Klopstock, Thomas; Fogel, Brent; Meijer, Inge; Rouleau, Guy; Bouchard, Jean-Pierre L.; Ganapathiraju, Madhavi; Vanderver, Adeline; Dahl, Niklas; Hobson, Grace; Brusco, Alfredo; Brussino, Alessandro; Padiath, Quasar Saleem
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收藏UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosisUBQLN2突变在法国和法国-加拿大肌萎缩性侧索硬化症中很少见
Daoud, Hussein; Suhail, Hamid; Szuto, Anna; Camu, William; Salachas, Francois; Meininger, Vincent; Bouchard, Jean-Pierre; Dupre, Nicolas; Dion, Patrick A.; Rouleau, Guy A.
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收藏Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis
Gros-Louis, Francois; Andersen, Peter M.; Dupre, Nicolas; Urushitani, Makoto; Dion, Patrick; Souchon, Frederique; D'Amour, Monique; Camu, William; Meininger, Vincent; Bouchard, Jean-Pierre; Rouleau, Guy A.; Julien, Jean-Pierre
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