Dilated cardiomyopathy in patients with mutations in anoctamin 5 von Wahbi, K, Béhin, A, Bécane, H.M, Leturcq, F, Cossée, M, Laforêt, P, Stojkovic, T, Carlier, P, Toussaint, M, Gaxotte, V, Cluzel, P, Eymard, B, Duboc, D

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D.P.3.02 Desminopathies: What can we learn from a long term follow-up? von Behin, A, Stojkovic, T, Claeys, K, Wahbi, K, Duboc, D, Becane, H.M, Dubourg, O, Maisonobe, T, Stoltenburg, G, Fardeau, M, Richard, P, Goudeau, B, Vicart, P, Eymard, B

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NMO03 Phenotypic heterogeneity of Duchenne muscular dystrophy assessed by long term follow-up and role of the endomysial fibrosis in the muscle von Desguerre, I, Christov, C, Mayer, M, Becane, H.M, Zeller, R, Chelly, J, Gherardi, R

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S.P.27 Electrophysiological study with prophylactic pacing and survival in adults with myotonic dystrophy and conduction system disease von Wahbi, K, Meune, C, Porcher, R, Bécane, H.M, Lazarus, A, Laforet, P, Stojkovic, T, Béhin, A, Radvanyi-Hoffman, H, Eymard, B, Duboc, D

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Ventricular arrhythmia in Duchenne muscular dystrophy: Prevalence, significance and prognosis von Chenard, A.A., Becane, H.M., Tertrain, F., de Kermadec, J.M., Weiss, Y.A.

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A high prevalence of hypertension inpatients presenting with mitochondrial diseases von Chong-Nguyen, C., Laforêt, P., Goursot, Y., Bougoin, W., Behin, A., Stojkovic, T., Becane, H.M., Jardel, C., Berber, N., Mochel, F., Lombes, A., Eymard, B., Duboc, D., Wahbi, K.

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Incidence and predictors of venous thromboembolism in inherited myopathies: A higher risk in myotonic dystrophy von Sochala, M., Porcher, R., Laforet, P., Fayssoil, A., Becane, H.M., Lazarus, A., Stojkovic, T., Behin, A., Leonard-Louis, S., Arnaud, P., Furling, D., Bassez, G., Eymard, B., Duboc, D., Wahbi, K.

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G.P.14.02 A high prevalence of Brugada syndrome among patients with Steinert’s disease: A new insight into the pathophysiology of Steinert’s disease’s cardiac complications von Wahbi, K, Fressart, V, Bécane, H.M, Meune, C, Richard, P, Lazarus, A, Laforêt, P, Benammar, N, Radvanyi-Hoffman, H, Eymard, B, Duboc, D

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Hypertrophic cardiomyopathy in glycogen storage disease type III: Clinical features and long-term outcome von Chong-Nguyen, C., Fayssoil, A., Laforet, P., Gajdos, V., Petit, F., Hubert, A., Kachetel, K., Bécane, H.M., Stojkovic, T., Eymard, B., Labrune, P., Wahbi, K.

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Association between mutation size and cardiac involvement in myotonic dystrophy type 1: when size matters von Chong-Nguyen, C., Wahbi, K., Algalarrondo, V., Bécane, H.M., Radvanyi-Hoffman, H., Arnaud, P., Furling, D., Bassez, G., Lazarus, A., Laforet, P., Stojkovic, T., Behin, A., Fayssoil, A., Eymard, B., Duboc, D.

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Effect of Perindopril on the Onset and Progression of Left Ventricular Dysfunction in Duchenne Muscular Dystrophy von Duboc, D., Meune, C., Lerebours, G., Devaux, J.Y., Vaksmann, G., Becane, H.M.

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Errance diagnostique dans les myopathies mitochondriales : étude de 12 patients thymectomisés von Ben Yaou, R., Laforêt, P., Bécane, H.M., Jardel, C., Sternberg, D., Lombès, A., Eymard, B.

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