Diversity of ARSACS Mutations in French-Canadians von Thiffault, I., Dicaire, M.J., Tetreault, M., Huang, K.N., Demers-Lamarche, J., Bernard, G., Duquette, A., Larivière, R., Gehring, K., Montpetit, A., McPherson, P.S., Richter, A., Montermini, L., Mercier, J., Mitchell, G.A., Dupré, N., Prévost, C., Bouchard, J.P., Mathieu, J., Brais, B.

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Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains von Lavoie, Hugo, Debeane, François, Trinh, Quoc-Dien, Turcotte, Jean-François, Corbeil-Girard, Louis-Philippe, Dicaire, Marie-Josée, Saint-Denis, Anik, Pagé, Martin, Rouleau, Guy A., Brais, Bernard

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PABPN1 overexpression leads to upregulation of genes encoding nuclear proteins that are sequestered in oculopharyngeal muscular dystrophy nuclear inclusions von Corbeil-Girard, Louis-Philippe, Klein, Arnaud F., Sasseville, A. Marie-Josée, Lavoie, Hugo, Dicaire, Marie-Josée, Saint-Denis, Anik, Pagé, Martin, Duranceau, André, Codère, François, Bouchard, Jean-Pierre, Karpati, George, Rouleau, Guy A., Massie, Bernard, Langelier, Yves, Brais, Bernard

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Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians von RODDIER, K, THOMAS, T, VANASSE, M, GAUDET, D, ROULEAU, G. A, BRAIS, B, MARLEAU, G, GAGNON, A. M, DICAIRE, M. J, ST.-DENIS, A, GOSSELIN, I, SARRAZIN, A. M, LARBRISSEAU, A, LAMBERT, M

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The FGF14 GAA repeat expansion in Greek patients with late-onset cerebellar ataxia and an overview of the SCA27B phenotype across populations von Kartanou, C, Mitrousias, A, Pellerin, D, Kontogeorgiou, Z, Iruzubieta, P, Dicaire, MJ, Danzi, MC, Koniari, C, Athanassopoulos, K, Panas, M, Stefanis, L, Zuchner, S, Brais, B, Houlden, H, Karadima, G, Koutsis, G

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Optimized testing strategy for the diagnosis of GAA-FGF14 ataxia/spinocerebellar ataxia 27B von Bonnet, C, Pellerin, D, Roth, V, Clément, G, Wandzel, M, Lambert, L, Frismand, S, Douarinou, M, Grosset, A, Bekkour, I, Weber, F, Girardier, F, Robin, C, Cacciatore, S, Bronner, M, Pourié, C, Dreumont, N, Puisieux, S, Iruzubieta, P, Dicaire, MJ, Evoy, F, Rioux, MF, Hocquel, A, La Piana, R, Synofzik, M, Houlden, H, Danzi, MC, Zuchner, S, Brais, B, Renaud, M

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Frequency and phenotypic spectrum of spinocerebellar ataxia 27B and other genetic ataxias in a Spanish cohort of late-onset cerebellar ataxia von Iruzubieta, P, Pellerin, D, Bergareche, A, Albajar, I, Mondragón, E, Vinagre, A, Fernández-Torrón, R, Moreno, F, Equiza, J, Campo-Caballero, D, Poza, JJ, Ruibal, M, Formica, A, Dicaire, MJ, Danzi, MC, Zuchner, S, Croitoru, I, Ruiz, M, Schlüter, A, Casasnovas, C, Pujol, A, Brais, B, Houlden, H, López de Munain, A, Ruiz-Martínez, J

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