Meune, C., Avouac, J., Airo, P., Beretta, L., Dieude, P., Wahbi, K., Caramaschi, P., Tiev, K., Cappelli, S., Diot, E., Vacca, A., Cracowski, J. L., Sibilia, J., Kahan, A., Matucci-Cerinic, M., Allanore, Y. :
Prediction of pulmonary hypertension related to systemic sclerosis by an index based on simple clinical observations
Arthritis Rheum, 2011 ; 63 (9) : 2790-2796
Publications (1184)
Wahbi, K., Ederhy, S., Becane, H. M., Meune, C., Behin, A., Stojkovic, T., Laforet, P., Eymard, B., Duboc, D., Cohen, A. :
Impaired myocardial deformation detected by speckle-tracking echocardiography in patients with myotonic dystrophy type 1 Int J Cardiol, 2011 ; 152 (3) : 375-376
Impaired myocardial deformation detected by speckle-tracking echocardiography in patients with myotonic dystrophy type 1 Int J Cardiol, 2011 ; 152 (3) : 375-376
Boontje, N. M., Merkus, D., Zaremba, R., Versteilen, A., de Waard, M. C., Mearini, G., de Beer, V. J., Carrier, L., Walker, L. A., Niessen, H. W., Dobrev, D., Stienen, G. J., Duncker, D. J., van der Velden, J. :
Enhanced myofilament responsiveness upon beta-adrenergic stimulation in post-infarct remodeled myocardium J Mol Cell Cardiol, 2011 ; 50 (3) : 487-499
Enhanced myofilament responsiveness upon beta-adrenergic stimulation in post-infarct remodeled myocardium J Mol Cell Cardiol, 2011 ; 50 (3) : 487-499
Hourez, R., Servais, L., Orduz, D., Gall, D., Millard, I., de Kerchove d'Exaerde, A., Cheron, G., Orr, H. T., Pandolfo, M., Schiffmann, S. N. :
Aminopyridines correct early dysfunction and delay neurodegeneration in a mouse model of spinocerebellar ataxia type 1 J Neurosci, 2011 ; 31 (33) : 11795-807
Aminopyridines correct early dysfunction and delay neurodegeneration in a mouse model of spinocerebellar ataxia type 1 J Neurosci, 2011 ; 31 (33) : 11795-807
Payan, C. A., Viallet, F., Landwehrmeyer, B. G., Bonnet, A. M., Borg, M., Durif, F., Lacomblez, L., Bloch, F., Verny, M., Fermanian, J., Agid, Y., Ludolph, A. C., Leigh, P. N., Bensimon, G. :
Disease Severity and Progression in Progressive Supranuclear Palsy and Multiple System Atrophy: Validation of the NNIPPS – PARKINSON PLUS SCALE PLoS ONE, 2011 ; 6 (8) : e22293
Disease Severity and Progression in Progressive Supranuclear Palsy and Multiple System Atrophy: Validation of the NNIPPS – PARKINSON PLUS SCALE PLoS ONE, 2011 ; 6 (8) : e22293
Baligand, C., Gilson, H., Menard, J. C., Schakman, O., Wary, C., Thissen, J. P., Carlier, P. G. :
Functional assessment of skeletal muscle in intact mice lacking myostatin by concurrent NMR imaging and spectroscopy Gene Ther, 2010 ; 17 (3) : 328-37
Functional assessment of skeletal muscle in intact mice lacking myostatin by concurrent NMR imaging and spectroscopy Gene Ther, 2010 ; 17 (3) : 328-37
Fressart, V., Duthoit, G., Donal, E., Probst, V., Deharo, J. C., Chevalier, P., Klug, D., Dubourg, O., Delacretaz, E., Cosnay, P., Scanu, P., Extramiana, F., Keller, D., Hidden-Lucet, F., Simon, F., Bessirard, V., Roux-Buisson, N., Hebert, J. L., Azarine, A., Casset-Senon, D., Rouzet, F., Lecarpentier, Y., Fontaine, G., Coirault, C., Frank, R., Hainque, B., Charron, P. :
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice Europace, 2010 ; 12 (6) : 861-868
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice Europace, 2010 ; 12 (6) : 861-868
Mochel, F., Duteil, S., Marelli, C., Jauffret, C., Barles, A., Holm, J., Sweetman, L., Benoist, J. F., Rabier, D., Carlier, P. G., Durr, A. :
Dietary anaplerotic therapy improves peripheral tissue energy metabolism in patients with Huntington’s disease Eur J Hum Genet, 2010 ; 18 (9) : 1057-1060
Dietary anaplerotic therapy improves peripheral tissue energy metabolism in patients with Huntington’s disease Eur J Hum Genet, 2010 ; 18 (9) : 1057-1060
Wein, N., Avril, A., Bartoli, M., Beley, C., Chaouch, S., Laforet, P., Behin, A., Butler-Browne, G., Mouly, V., Krahn, M., Garcia, L., Levy, N. :
Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skipping Hum Mutat, 2010 ; 31 (2) :
Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skipping Hum Mutat, 2010 ; 31 (2) :
Laforêt, P :
Cerebral vessel involvement in Pompe disease. The Steps Forward in Pompe Disease -3rd European Symposium, Munich, Germany, November 20 and 21 2009 Clin Ther, 2010 ; 32 (Supplement 2) : S51
Cerebral vessel involvement in Pompe disease. The Steps Forward in Pompe Disease -3rd European Symposium, Munich, Germany, November 20 and 21 2009 Clin Ther, 2010 ; 32 (Supplement 2) : S51
