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A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.
Lafrenière RG, Cader MZ, Poulin JF, Andres-Enguix I, Simoneau M, Gupta N, Boisvert K, Lafrenière F, McLaughlan S, Dubé MP, Marcinkiewicz MM, Ramagopalan S, Ansorge O, Brais B, Sequeiros J, Pereira-Monteiro JM, Griffiths LR, Tucker SJ, Ebers G, Rouleau GA. Lafrenière RG, et al. Among authors: brais b. Nat Med. 2010 Oct;16(10):1157-60. doi: 10.1038/nm.2216. Epub 2010 Sep 26. Nat Med. 2010. PMID: 20871611
Recent studies on oculopharyngeal muscular dystrophy in Québec.
Bouchard JP, Brais B, Brunet D, Gould PV, Rouleau GA. Bouchard JP, et al. Among authors: brais b. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S22-9. doi: 10.1016/s0960-8966(97)00077-1. Neuromuscul Disord. 1997. PMID: 9392011
Twenty-one families have taken part in the study, which led to our localization of the gene in 1995 [Brais B, Xie Y-G, Sanson M, et al. Hum Mol Genet 1995; 4:429-434]. ...
Twenty-one families have taken part in the study, which led to our localization of the gene in 1995 [Brais B, Xie Y-G, Sanson …
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.
Brais B, Bouchard JP, Xie YG, Rochefort DL, Chrétien N, Tomé FM, Lafrenière RG, Rommens JM, Uyama E, Nohira O, Blumen S, Korczyn AD, Heutink P, Mathieu J, Duranceau A, Codère F, Fardeau M, Rouleau GA. Brais B, et al. Nat Genet. 1998 Feb;18(2):164-7. doi: 10.1038/ng0298-164. Nat Genet. 1998. PMID: 9462747
Oculopharyngeal muscular dystrophy.
Brais B, Rouleau GA, Bouchard JP, Fardeau M, Tomé FM. Brais B, et al. Semin Neurol. 1999;19(1):59-66. doi: 10.1055/s-2008-1040826. Semin Neurol. 1999. PMID: 10711989 Review.
209 results