Catelain, C., Riveron, S., Papadopoulos, A., Mougenot, N., Jacquet, A., Vauchez, K., Yada, E., Puceat, M., Fiszman, M., Butler-Browne, G., Bonne, G., Vilquin, J. T. :
Myoblasts and Embryonic Stem Cells Differentially Engraft in a Mouse Model of Genetic Dilated Cardiomyopathy
Mol Ther, 2013 ; 21 (5) : 1064-1075
Publications (1184)
Mademan, I., Deconinck, T., Dinopoulos, A., Voit, T., Schara, U., Devriendt, K., Meijers, B., Lerut, E., De Jonghe, P., Baets, J. :
De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy Neurology, 2013 ; 81 (22) : 1953-8
De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy Neurology, 2013 ; 81 (22) : 1953-8
Cattin, M. E., Muchir, A., Bonne, G. :
‘State-of-the-heart’ of cardiac laminopathies Curr Opin Cardiol, 2013 ; 28 (3) : 297-304
‘State-of-the-heart’ of cardiac laminopathies Curr Opin Cardiol, 2013 ; 28 (3) : 297-304
Hervier, B., Devilliers, H., Benveniste, O. :
Patients with non-Jo-1 anti-RNA-synthetase autoantibodies have worse survival than Jo-1 positive patients Ann Rheum Dis, 2013 ; 72 (7) : e18
Patients with non-Jo-1 anti-RNA-synthetase autoantibodies have worse survival than Jo-1 positive patients Ann Rheum Dis, 2013 ; 72 (7) : e18
Chenevier-Gobeaux, C., Meune, C., Freund, Y., Wahbi, K., Claessens, Y. E., Doumenc, B., Zuily, S., Riou, B., Ray, P. :
Influence of Age and Renal Function on High-Sensitivity Cardiac Troponin T Diagnostic Accuracy for the Diagnosis of Acute Myocardial Infarction Am J Cardiol, 2013 ; 111 (12) : 1701-1707
Influence of Age and Renal Function on High-Sensitivity Cardiac Troponin T Diagnostic Accuracy for the Diagnosis of Acute Myocardial Infarction Am J Cardiol, 2013 ; 111 (12) : 1701-1707
Laforet, P., Stojkovic, T., Bassez, G., Carlier, P. G., Clement, K., Wahbi, K., Petit, F. M., Eymard, B., Carlier, R. Y. :
Neutral lipid storage disease with myopathy: A whole-body nuclear MRI and metabolic study Mol Genet Metab, 2013 ; 108 (2) : 125-31
Neutral lipid storage disease with myopathy: A whole-body nuclear MRI and metabolic study Mol Genet Metab, 2013 ; 108 (2) : 125-31
Moore, S., Ribes, V., Terriente, J., Wilkinson, D., Relaix, F., Briscoe, J. :
Distinct regulatory mechanisms act to establish and maintain pax3 expression in the developing neural tube PLoS Genet, 2013 ; 9 (10) : e1003811
Distinct regulatory mechanisms act to establish and maintain pax3 expression in the developing neural tube PLoS Genet, 2013 ; 9 (10) : e1003811
Martins, P. C., Ayub-Guerrieri, D., Martins-Bach, A. B., Onofre-Oliveira, P., Malheiros, J. M., Tannus, A., de Sousa, P. L., Carlier, P. G., Vainzof, M. :
Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies Dis Model Mech, 2013 ; 6 (5) : 1167-74
Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies Dis Model Mech, 2013 ; 6 (5) : 1167-74
Hogrel, J. Y., Zagnoli, F., Canal, A., Fraysse, B., Bouchard, J. P., Skuk, D., Fardeau, M., Tremblay, J. P. :
Assessment of a symptomatic Duchenne muscular dystrophy carrier 20years after myoblast transplantation from her asymptomatic identical twin sister Neuromuscul Disord, 2013 ; 23 (7) : 575-9
Assessment of a symptomatic Duchenne muscular dystrophy carrier 20years after myoblast transplantation from her asymptomatic identical twin sister Neuromuscul Disord, 2013 ; 23 (7) : 575-9
Bozorgmehr, B., Kariminejad, A., Nafissi, S., Jebelli, B., Andoni, U., Gartioux, C., Ledeuil, C., Allamand, V., Richard, P., Kariminejad, M. H. :
Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic Correlations Iran J Child Neurol, 2013 ; 7 (3) : 15-22
Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic Correlations Iran J Child Neurol, 2013 ; 7 (3) : 15-22
