Evaluation of predictive models in daily practice for the identification of patients with Lynch syndrome von Tresallet, Christophe, Brouquet, Antoine, Julié, Catherine, Beauchet, Alain, Vallot, Céline, Ménégaux, Fabrice, Mitry, Emmanuel, Radvanyi, François, Malafosse, Robert, Rougier, Philippe, Nordlinger, Bernard, Laurent-Puig, Pierre, Boileau, Catherine, Emile, Jean-François, Muti, Christine, Penna, Christophe, Hofmann-Radvanyi, Hélène

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MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1 von Huin, Vincent, Vasseur, Francis, Schraen-Maschke, Susanna, Dhaenens, Claire-Marie, Devos, Patrick, Dupont, Kathy, Sergeant, Nicolas, Buée, Luc, Lacour, Arnaud, Hofmann-Radvanyi, Hélène, Sablonnière, Bernard

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Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1 von Chong-Nguyen, Caroline, Karim, Wahbi, Algalarrondo Vincent, Bécane, Henri Marc, Radvanyi-Hoffman, Hélène, Arnaud, Pauline, Furling Denis, Lazarus, Arnaud, Bassez Guillaume, Béhin Anthony, Fayssoil Abdallah, Laforêt Pascal, Stojkovic, Tanya, Eymard Bruno, Duboc Denis

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Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability von SEZNEC, H, LIA-BALDINI, A.-S, DUROS, C, FOUQUET, C, LACROIX, C, HOFMANN-RADVANYI, H, JUNIEN, C, GOURDON, G

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Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry von Chong-Nguyen, Caroline, Wahbi, Karim, Algalarrondo, Vincent, Bécane, Henri Marc, Radvanyi-Hoffman, Hélène, Arnaud, Pauline, Furling, Denis, Lazarus, Arnaud, Bassez, Guillaume, Béhin, Anthony, Fayssoil, Abdallah, Laforêt, Pascal, Stojkovic, Tanya, Eymard, Bruno, Duboc, Denis

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A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1) von Angeard, Nathalie, Jacquette, Aurélia, Gargiulo, Marcela, Radvanyi, Hélène, Moutier, Sylvain, Eymard, Bruno, Héron, Delphine

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Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: A case control study von Wahbi, Karim, Meune, Christophe, Bécane, Henri Marc, Laforêt, Pascal, Bassez, Guillaume, Lazarus, Arnaud, Radvanyi-Hoffman, Hélène, Eymard, Bruno, Duboc, Denis

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No evidence of somatic FGFR3 mutation in various types of carcinoma von KAROUI, Mehdi, HOFMANN-RADVANYI, Hélène, CHARBONNIER, Peggy, TRESALLET, Christophe, MITRY, Emmanuel, PENNA, Christophe, ROUGIER, Philippe, BOILEAU, Catherine, THIERY, Jean-Paul, NORDLINGER, Bernard, FRANC, Brigitte, RADVANYI, Francois, ZIMMERMANN, Ute, COUVELARD, Anne, DEGOTT, Claude, FARIDONI-LAURENS, Laetitia, AHOMADEGBE, Jean-Charles, GAZZERI, Sylvie, BRAMBILLA, Elisabeth, CLERICI, Thierry

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Electrophysiological Study With Prophylactic Pacing and Survival in Adults With Myotonic Dystrophy and Conduction System Disease von Wahbi, Karim, Meune, Christophe, Porcher, Raphaël, Bécane, Henri Marc, Lazarus, Arnaud, Laforêt, Pascal, Stojkovic, Tanya, Béhin, Anthony, Radvanyi-Hoffmann, Hélène, Eymard, Bruno, Duboc, Denis

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Cognitive profile in childhood myotonic dystrophy type 1: Is there a global impairment? von Angeard, Nathalie, Gargiulo, Marcela, Jacquette, Aurélia, Radvanyi, Hélène, Eymard, Bruno, Héron, Delphine

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Type 2 Myotonic Dystrophy Can Be Predicted by the Combination of Type 2 Muscle Fiber Central Nucleation and Scattered Atrophy von Bassez, Guillaume, Chapoy, Elisabeth, Bastuji-Garin, Sylvie, Radvanyi-Hoffman, Hélène, Authier, Francois-Jérôme, Pellissier, Jean François, Eymard, Bruno, Gherardi, Romain K

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Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1 von Wahbi, Karim, Algalarrondo, Vincent, Bécane, Henri Marc, Fressart, Véronique, Beldjord, Chérif, Azibi, Kamel, Lazarus, Arnaud, Berber, Nawal, Radvanyi-Hoffman, Hélène, Stojkovic, Tanya, Béhin, Anthony, Laforêt, Pascal, Eymard, Bruno, Hatem, Stéphane, Duboc, Denis

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Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon von Annane, Djillali, Fiorelli, Marco, Mazoyer, Bernard, Pappata, Sabina, Eymard, Bruno, Radvanyi, Hélène, Junien, Claudine, Fardeau, Michel, Merlet, Pascal, Gajdos, Philippe, Syrota, André, Sansom, Yves, Duboc, Denis

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Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice von Junien, Claudine, Gourdon, Geneviève, Blanche, Martine, Duros, Chantal, Abitbol, Marc, Hofmann-Radvanyi, Hlène, Radvanyi, François, Lia, Anne-Sophie

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Somatic Instability of the CTG Repeat in Mice Transgenic for the Myotonic Dystrophy Region is Age Dependent But Not Correlated to the Relative Intertissue Transcription Levels and... von Lia, Anne-Sophie, Seznec, Hervé, Hofmann-Radvanyi, Hélène, Radvanyi, François, Duros, Chantal, Saquet, Céline, Blanche, Martine, Junien, Claudine, Gourdon, Geneviève

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Myotonic dystrophy : size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism von LAVEDAN, C, HOFMANN-RADVANYI, H, SHELBOURNE, P, RABES, J.-P, DUROS, C, SAVOY, D, DEHAUPAS, I, LUCE, S, JOHNSON, K, JUNIEN, C

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Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy von Amiel, Jeanne, Raclin, Valérie, Jouannic, Jean-Marie, Morichon, Nicole, Hoffman-Radvanyi, Hélène, Dommergues, Marc, Feingold, Josué, Munnich, Arnold, Bonnefont, Jean-Paul

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Dystrophie myotonique de type 2 révélée par un syndrome parkinsonien et des troubles cognitifs von Bouquet, Floriane, Stojkovic, Tanya, Maisonobe, Thierry, Michon, Claire-Cécile, Radvanyi, Hélène, Eymard, Bruno

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Blunted coronary reserve in myotonic dystrophy : An early and gene-related phenomenon von ANNANE, D, MERLET, P, SYROTA, A, DUBOC, D, RADVANYI, H, MAZOYER, B, EYMARD, B, FIORELLI, M, JUNIEN, C, FARDEAU, M, OUNNOUGHENE, Z, GAJDOS, P

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Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele von Hofmann-Radvanyi, Hélène, Lavedan, Christian, Rabès, Jean-Pierre, Savoy, Daniel, Duros, Chantal, Johnson, Keith, Junien, Claudine

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