Ternary feldspar thermometry of Paleoproterozoic granulites from In-Ouzzal terrane (Western Hoggar, southern Algeria) von Benbatta, A., Bendaoud, A., Cenki-Tok, B., Adjerid, Z., Lacène, K., Ouzegane, K.

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Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies von Arimura, Takuro, Helbling-Leclerc, Anne, Massart, Catherine, Varnous, Shaida, Niel, Florence, Lacène, Emmanuelle, Fromes, Yves, Toussaint, Marcel, Mura, Anne-Marie, Keller, Dagmar I., Amthor, Helge, Isnard, Richard, Malissen, Marie, Schwartz, Ketty, Bonne, Gisèle

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Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation von Auré, Karine, Fayet, Guillemette, Leroy, Jean Paul, Lacène, Emmanuelle, Romero, Norma Beatriz, Lombès, Anne

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Binary comparative study adsorption of anionic and cationic Azo-dyes on Fe3O4-Bentonite magnetic nanocomposite: Kinetics, Equilibrium, Mechanism and Thermodynamic study von Oukebdane, K., Necer, I. Lacene, Didi, M. A.

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FP.05 From the Muscle Atlas to an AI-based diagnostic tool von Meyer, C., Lacene, E., Beuvin, M., Evangelista, T., Laporte, J., Jeannin-Girardon, A., Collet, P., Poch, O., Romero, N., Chennen, K., Cadot, B.

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OTHER NMDs: EP.355 Comprehensive morphometric assessment of skeletal muscle development from birth to 18 years von Evangelista, T., Kandji, M., Lacene, M., Chanut, A., BUI, M. Thao, Marty, R., Buffat, L., Knobloch, K., Rudkin, B.B., Romero, N.B.

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OTHER NMDs von Evangelista, T., Kandji, M., Lacene, M., Chanut, A., BUI, M. Thao, Marty, R., Buffat, L., Knobloch, K., Rudkin, B.B., Romero, N.B.

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P.77Repurposing of metformin identified as a potential therapy in models of BAG3 myofibrillar myopathy von Ruparelia, A., McKaige, E., Williams, C., Schulze, K., Fuchs, M., Oorschot, V., Lacene, E., Mirella, M., Baxter, E., Torrente, Y., Ramm, G., Stojkovic, T., Lavoié, J., Bryson-Richardson, R.

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G.P.1 07 AMP-activated protein kinase gene mutation: a new cause of muscular glycogenosis associated with hypertrophic cardiomyopathy and conduction defect von Laforêt, P., Richard, P., Aït Saïd, M., Romero, N.B., Lacène, E., Leroy, J.-P., Baussan, C., Hogrel, J.-Y., Lavergne, T., Wahbi, K., Hainque, B., Duboc, D.

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A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis von Laforêt, Pascal, Richard, Pascale, Said, Mina Ait, Romero, Norma Beatriz, Lacene, Emmanuelle, Leroy, Jean-Paul, Baussan, Christiane, Hogrel, Jean-Yves, Lavergne, Thomas, Wahbi, Karim, Hainque, Bernard, Duboc, Denis

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