Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations von Sébillon, P, Bouchier, C, Bidot, L D, Bonne, G, Ahamed, K, Charron, P, Drouin-Garraud, V, Millaire, A, Desrumeaux, G, Benaïche, A, Charniot, J-C, Schwartz, K, Villard, E, Komajda, M

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Danon’s disease as a cause of hypertrophic cardiomyopathy: a systematic survey von Charron, P, Villard, E, Sébillon, P, Laforêt, P, Maisonobe, T, Duboscq-Bidot, L, Romero, N, Drouin-Garraud, V, Frébourg, T, Richard, P, Eymard, B, Komajda, M

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COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fe... von Flavigny, Jeanne, Souchet, Michel, Sébillon, Pascale, Berrebi-Bertrand, Isabelle, Hainque, Bernard, Mallet, Alain, Bril, Antoine, Schwartz, Ketty, Carrier, Lucie

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Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients von Postma, A V, Denjoy, I, Kamblock, J, Alders, M, Lupoglazoff, J-M, Vaksmann, G, Dubosq-Bidot, L, Sebillon, P, Mannens, M M A M, Guicheney, P, Wilde, A A M

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Danon’s disease as a cause of hypertrophic cardiomyopathy: a systematic survey von Charron, P, Villard, E, Sébillon, P, Laforêt, P, Maisonobe, T, Duboscq-Bidot, L, Romero, N, Drouin-Garraud, V, Frébourg, T, Richard, P, Eymard, B, Komajda, M

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A T to G mutation in the polypyrimidine tract of the second intron of the human β-globin gene reduces in vitro splicing efficiency: evidence for an increased hnRNP C interaction von Sébillon, Pascale, Beldjord, Chérif, Kaplan, Jean-Claude, Brody, Edward, Marie, Joēlle

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Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia von Postma, Alex V, Denjoy, Isabelle, Hoorntje, Theo M, Lupoglazoff, Jean-Marc, Da Costa, Antoine, Sebillon, Pascale, Mannens, Marcel M.A.M, Wilde, Arthur A.M, Guicheney, Pascale

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Charcot-Marie-tooth features and maculopathy in a patient with Danon disease von LAFORET, P, CHARRON, P, EYMARD, B, MAISONOBE, T, ROMERO, N. B, VILLARD, E, SEBILLON, P, DROUIN-GARRAUD, V, DUBOURG, O, FARDEAU, M, KOMAJDA, M

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Influence of mobilized stem cells on myocardial infarct repair in a nonhuman primate model von Norol, Françoise, Merlet, Pascal, Isnard, Richard, Sebillon, Pascale, Bonnet, Nicolas, Cailliot, Christian, Carrion, Claire, Ribeiro, Maria, Charlotte, Frédéric, Pradeau, Pascal, Mayol, Jean-François, Peinnequin, André, Drouet, Michel, Safsafi, Karima, Vernant, Jean-Paul, Herodin, Francis

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Functional consequences of an LMNA mutation associated with a new cardiac and non‐cardiac phenotype von Charniot, Jean‐Christophe, Pascal, Cécile, Bouchier, Christiane, Sébillon, Pascale, Salama, Jeffrey, Duboscq‐Bidot, Laëtitia, Peuchmaurd, Mireille, Desnos, Michel, Artigou, Jean‐Yves, Komajda, Michel

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COOH-terminal truncated human cardiac MyBP-C alters myosin filament organization von Sébillon, Pascale, Bonne, Gisèle, Flavigny, Jeanne, Venin, Sophie, Rouche, Andrée, Fiszman, Marc, Vikstrom, Karen, Leinwand, Leslie, Carrier, Lucie, Schwartz, Ketty

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Mutational analysis of the β- and δ-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy von Sylvius, Nicolas, Duboscq-Bidot, Laetitia, Bouchier, Christiane, Charron, Philippe, Benaiche, Abdelaziz, Sébillon, Pascale, Komajda, Michel, Villard, Eric

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Rapid and Direct Detection of the Most Frequent Mediterranean β-Thalassemic Mutations by Multiplex Allele-Specific Enzymatic Amplification von BIENVENU, THIERRY, SEBILLON, PASCALE, LABIE, DOMINIQUE, KAPLAN, JEAN CLAUDE, BELDJORD, CHERIF

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Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and unctional consequences of these mutations von SEBILLON, P, BOUCHIER, C, CHARNIOT, J-C, SCHWARTZ, K, VILLARD, E, KOMAJDA, M, BIDOT, L. D, BONNE, G, AHAMED, K, CHARRON, P, DROUIN-GARRAUD, V, MILLAIRE, A, DESRUMEAUX, G, BENAÏCHE, A

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Detection of the Most Frequent β-Thalassemic Defect in Southeast Asia by PCR von Sebillon, P., Bienvenu, T., Girot, R., Labie, D., Kaplan, J. C., Beldjord, C.

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