Nebel, M., Schwoerer, A. P., Warszta, D., Siebrands, C. C., Limbrock, A. C., Swarbrick, J. M., Fliegert, R., Weber, K., Bruhn, S., Hohenegger, M., Geisler, A., Herich, L., Schlegel, S., Carrier, L., Eschenhagen, T., Potter, B. V., Ehmke, H., Guse, A. H. :
NAADP mediated calcium signalling and arrhythmias in the heart evoked by beta-adrenergic stimulation
J Biol Chem, 2013 ; 288 (22) : 16017-16030
Publications (1181)
Benkhelifa-Ziyyat, S., Besse, A., Roda, M., Duque, S., Astord, S., Carcenac, R., Marais, T., Barkats, M. :
Intramuscular scAAV9-SMN Injection Mediates Widespread Gene Delivery to the Spinal Cord and Decreases Disease Severity in SMA Mice Mol Ther, 2013 ; 21 (2) : 282-90
Intramuscular scAAV9-SMN Injection Mediates Widespread Gene Delivery to the Spinal Cord and Decreases Disease Severity in SMA Mice Mol Ther, 2013 ; 21 (2) : 282-90
Willis, T. A., Hollingsworth, K. G., Coombs, A., Sveen, M. L., Andersen, S., Stojkovic, T., Eagle, M., Mayhew, A., de Sousa, P. L., Dewar, L., Morrow, J. M., Sinclair, C. D., Thornton, J. S., Bushby, K., Lochmuller, H., Hanna, M. G., Hogrel, J. Y., Carlier, P. G., Vissing, J., Straub, V. :
Quantitative Muscle MRI as an Assessment Tool for Monitoring Disease Progression in LGMD2I: A Multicentre Longitudinal Study PLoS ONE, 2013 ; 8 (8) : e70993
Quantitative Muscle MRI as an Assessment Tool for Monitoring Disease Progression in LGMD2I: A Multicentre Longitudinal Study PLoS ONE, 2013 ; 8 (8) : e70993
Popplewell, L., Koo, T., Leclerc, X., Duclert, A., Mamchaoui, K., Gouble, A., Mouly, V., Voit, T., Paques, F., Cedrone, F., Isman, O., Yanez-Munoz, R. J., Dickson, G. :
Gene correction of a duchenne muscular dystrophy mutation by meganuclease-enhanced exon knock-in Hum Gene Ther, 2013 ; 24 (7) : 692-701
Gene correction of a duchenne muscular dystrophy mutation by meganuclease-enhanced exon knock-in Hum Gene Ther, 2013 ; 24 (7) : 692-701
Le Hir, M., Goyenvalle, A., Peccate, C., Precigout, G., Davies, K. E., Voit, T., Garcia, L., Lorain, S. :
AAV Genome Loss From Dystrophic Mouse Muscles During AAV-U7 snRNA-mediated Exon-skipping Therapy Mol Ther, 2013 ; 21 (8) : 1551-1558
AAV Genome Loss From Dystrophic Mouse Muscles During AAV-U7 snRNA-mediated Exon-skipping Therapy Mol Ther, 2013 ; 21 (8) : 1551-1558
Hourde, C., Joanne, P., Medja, F., Mougenot, N., Jacquet, A., Mouisel, E., Pannerec, A., Hatem, S., Butler-Browne, G., Agbulut, O., Ferry, A. :
Voluntary Physical Activity Protects from Susceptibility to Skeletal Muscle Contraction-Induced Injury But Worsens Heart Function in mdx Mice Am J Pathol, 2013 ; 182 (5) : 1509-1518
Voluntary Physical Activity Protects from Susceptibility to Skeletal Muscle Contraction-Induced Injury But Worsens Heart Function in mdx Mice Am J Pathol, 2013 ; 182 (5) : 1509-1518
Romero, N. B., Clarke, N. F. :
Congenital myopathies Handb Clin Neurol, 2013 ; 113 : 1321-36
Congenital myopathies Handb Clin Neurol, 2013 ; 113 : 1321-36
Servais, L., Baudoin, H., Zehrouni, K., Richard, P., Sternberg, D., Fournier, E., Eymard, B., Stojkovic, T. :
Pregnancy in congenital myasthenic syndrome J Neurol, 2013 ; 260 (3) : 815-819
Pregnancy in congenital myasthenic syndrome J Neurol, 2013 ; 260 (3) : 815-819
Donadille, B., D'Anella, P., Auclair, M., Uhrhammer, N., Sorel, M., Grigorescu, R., Ouzounian, S., Cambonie, G., Boulot, P., Laforet, P., Carbonne, B., Christin-Maitre, S., Bignon, Y. J., Vigouroux, C. :
Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome Orphanet J Rare Dis, 2013 ; 8 (1) : 106
Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome Orphanet J Rare Dis, 2013 ; 8 (1) : 106
Voermans, N. C., Jungbluth, H., Brusse, E., van Engelen, B. G., Laforet, P. :
Exertional hyperCKemia might be the first manifestation of a genetic disorder Muscle Nerve, 2013 ; 48 (3) : 461-2
Exertional hyperCKemia might be the first manifestation of a genetic disorder Muscle Nerve, 2013 ; 48 (3) : 461-2
