Stanciu, R., Guiguet, M., Musset, L., Touitou, D., Beigelman, C., Rigolet, A., Costedoat-Chalumeau, N., Allenbach, Y., Hervier, B., Dubourg, O., Maisonobe, T., Charuel, J. L., Behin, A., Herson, S., Amoura, Z., Grenier, P., Benveniste, O. :
Antisynthetase Syndrome with Anti-Jo1 Antibodies in 48 Patients: Pulmonary Involvement Predicts Disease-modifying Antirheumatic Drug Use
J Rheumatol, 2012 ; 39 (9) : 1835-9
Publications (1184)
Borrego-Pinto, J., Jegou, T., Osorio, D. S., Aurade, F., Gorjanacz, M., Koch, B., Mattaj, I. W., Gomes, E. R. :
Samp1 is a component of TAN lines and is required for nuclear movement J Cell Sci, 2012 ; 125 (Pt 5) : 1099-10105
Samp1 is a component of TAN lines and is required for nuclear movement J Cell Sci, 2012 ; 125 (Pt 5) : 1099-10105
Hadj-Said, W., Bangratz, M., Vignaud, A., Chatonnet, A., Butler-Browne, G., Nicole, S., Agbulut, O., Ferry, A. :
Effect of locomotor training on muscle performance in the context of nerve-muscle communication dysfunction Muscle Nerve, 2012 ; 45 (4) : 567-577
Effect of locomotor training on muscle performance in the context of nerve-muscle communication dysfunction Muscle Nerve, 2012 ; 45 (4) : 567-577
Mochel, F., Schiffmann, R., Steenweg, M. E., Akman, H. O., Wallace, M., Sedel, F., Laforet, P., Levy, R., Powers, J. M., Demeret, S., Maisonobe, T., Froissart, R., Da Nobrega, B. B., Fogel, B. L., Natowicz, M. R., Lubetzki, C., Durr, A., Brice, A., Rosenmann, H., Barash, V., Kakhlon, O., Gomori, J. M., van der Knaap, M. S., Lossos, A. :
Adult polyglucosan body disease: Natural History and Key Magnetic Resonance Imaging Findings Ann Neurol, 2012 ; 72 (3) : 433-441
Adult polyglucosan body disease: Natural History and Key Magnetic Resonance Imaging Findings Ann Neurol, 2012 ; 72 (3) : 433-441
Wahbi, K., Behin, A., Charron, P., Dunand, M., Richard, P., Meune, C., Vicart, P., Laforet, P., Stojkovic, T., Becane, H. M., Kuntzer, T., Duboc, D. :
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study Neuromuscul Disord, 2012 ; 22 (3) : 211-218
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study Neuromuscul Disord, 2012 ; 22 (3) : 211-218
Bevilacqua, J. A., Monnier, N., Bitoun, M., Eymard, B., Ferreiro, A., Monges, S., Lubieniecki, F., Taratuto, A. L., Laquerriere, A., Claeys, K. G., Marty, I., Fardeau, M., Guicheney, P., Lunardi, J., Romero, N. B. :
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalisation and large areas of myofibrillar disorganisation Neuropathol Appl Neurobiol, 2011 ; 37 (3) : 271-284
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalisation and large areas of myofibrillar disorganisation Neuropathol Appl Neurobiol, 2011 ; 37 (3) : 271-284
Ho, A. T., Hayashi, S., Brohl, D., Aurade, F., Rattenbach, R., Relaix, F. :
Neural Crest Cell Lineage Restricts Skeletal Muscle Progenitor Cell Differentiation through Neuregulin1-ErbB3 Signaling Dev Cell, 2011 ; 21 (2) : 273-287
Neural Crest Cell Lineage Restricts Skeletal Muscle Progenitor Cell Differentiation through Neuregulin1-ErbB3 Signaling Dev Cell, 2011 ; 21 (2) : 273-287
Ono, Y., Calbaheu, F., Morgan, J. E., Katagiri, T., Amthor, H., Zammit, P. S. :
BMP signalling permits population expansion by preventing premature myogenic differentiation in muscle satellite cells Cell Death Differ, 2011 ; 18 (2) : 222-234
BMP signalling permits population expansion by preventing premature myogenic differentiation in muscle satellite cells Cell Death Differ, 2011 ; 18 (2) : 222-234
Cowling, B. S., Toussaint, A., Amoasii, L., Koebel, P., Ferry, A., Davignon, L., Nishino, I., Mandel, J. L., Laporte, J. :
Increased expression of wild-type or a centronuclear myopathy mutant of dynamin 2 in skeletal muscle of adult mice leads to structural defects and muscle weakness Am J Pathol, 2011 ; 178 (5) : 2224-35
Increased expression of wild-type or a centronuclear myopathy mutant of dynamin 2 in skeletal muscle of adult mice leads to structural defects and muscle weakness Am J Pathol, 2011 ; 178 (5) : 2224-35
Larue, S., Bombelli, F., Viala, K., Neil, J., Maisonobe, T., Bouche, P., Musset, L., Fournier, E., Leger, J. M. :
Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases Eur J Neurol, 2011 ; 18 (6) : 899-905
Non-anti-MAG DADS neuropathy as a variant of CIDP: clinical, electrophysiological, laboratory features and response to treatment in 10 cases Eur J Neurol, 2011 ; 18 (6) : 899-905
