van der Ploeg, A. T., Barohn, R., Carlson, L., Charrow, J., Clemens, P. R., Hopkin, R. J., Kishnani, P. S., Laforet, P., Morgan, C., Nations, S., Pestronk, A., Plotkin, H., Rosenbloom, B. E., Sims, K. B., Tsao, E. :
Open-label extension study following the Late-Onset Treatment Study (LOTS) of alglucosidase alfa
Mol Genet Metab, 2012 ; 107 (3) : 456-461
Publications (1184)
Charron, P, Arbustini, E, Bonne, G :
What should the cardiologist know about lamin disease ? Arrhythm Electrophysiol Rev, 2012 ; 1 (1) : 22-8
What should the cardiologist know about lamin disease ? Arrhythm Electrophysiol Rev, 2012 ; 1 (1) : 22-8
Hervier, B., Devilliers, H., Stanciu, R., Meyer, A., Uzunhan, Y., Masseau, A., Dubucquoi, S., Hatron, P. Y., Musset, L., Wallaert, B., Nunes, H., Maisonobe, T., Olsson, N. O., Adoue, D., Arlet, P., Sibilia, J., Guiguet, M., Lauque, D., Amoura, Z., Hachulla, E., Hamidou, M., Benveniste, O. :
Hierarchical cluster and survival analyses of antisynthetase syndrome: Phenotype and outcome are correlated with anti-tRNA synthetase antibody specificity Autoimmun Rev, 2012 ; 12 (2) : 210-7
Hierarchical cluster and survival analyses of antisynthetase syndrome: Phenotype and outcome are correlated with anti-tRNA synthetase antibody specificity Autoimmun Rev, 2012 ; 12 (2) : 210-7
Outteryck, O., de Seze, J., Stojkovic, T., Cuisset, J. M., Dobbelaere, D., Delalande, S., Lacour, A., Cabaret, M., Lepoutre, A. C., Deramecourt, V., Zephir, H., Fowler, B., Vermersch, P. :
Methionine synthase deficiency: A rare cause of adult-onset leukoencephalopathy Neurology, 2012 ; 79 (4) : 386-388
Methionine synthase deficiency: A rare cause of adult-onset leukoencephalopathy Neurology, 2012 ; 79 (4) : 386-388
Wargon, I., Richard, P., Kuntzer, T., Sternberg, D., Nafissi, S., Gaudon, K., Lebail, A., Bauche, S., Hantai, D., Fournier, E., Eymard, B., Stojkovic, T. :
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations Neuromuscul Disord, 2012 ; 22 (4) : 318-324
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations Neuromuscul Disord, 2012 ; 22 (4) : 318-324
Baudin, P. Y., Azzabou, N., Carlier, P. G., Paragios, N. :
Prior knowledge, random walks and human skeletal muscle segmentation Med Image Comput Comput Assist Interv - MICCAI, 2012 ; 15 (Pt 1) : 569-76
Prior knowledge, random walks and human skeletal muscle segmentation Med Image Comput Comput Assist Interv - MICCAI, 2012 ; 15 (Pt 1) : 569-76
Duboc, D., Wahbi, K. :
What is the best way to detect infra-Hisian conduction abnormalities and prevent sudden cardiac death in myotonic dystrophy? Heart, 2012 ; 98 (6) : 433-4
What is the best way to detect infra-Hisian conduction abnormalities and prevent sudden cardiac death in myotonic dystrophy? Heart, 2012 ; 98 (6) : 433-4
Laforet, P., Orngreen, M., Preisler, N., Andersen, G., Vissing, J. :
Blocked muscle fat oxidation during exercise in neutral lipid storage disease Arch Neurol, 2012 ; 69 (4) : 530-3
Blocked muscle fat oxidation during exercise in neutral lipid storage disease Arch Neurol, 2012 ; 69 (4) : 530-3
Sane, J., Kurkela, S., Desdouits, M., Kalimo, H., Mazalrey, S., Lokki, M. L., Vaheri, A., Helve, T., Tornwall, J., Huerre, M., Butler-Browne, G., Ceccaldi, P. E., Gessain, A., Vapalahti, O. :
Prolonged myalgia in Sindbis virus infection: case description and in vitro infection of myotubes and myoblasts J Infect Dis, 2012 ; 206 (3) : 407-414
Prolonged myalgia in Sindbis virus infection: case description and in vitro infection of myotubes and myoblasts J Infect Dis, 2012 ; 206 (3) : 407-414
Billot, S., Herve, D., Akman, H. O., Froissart, R., Baussan, C., Claeys, K. G., Piraud, M., Sedel, F., Mochel, F., Laforet, P. :
Acute but transient neurological deterioration revealing adult polyglucosan body disease J Neurol Sci, 2012 ; 324 (1-2) : 179-182
Acute but transient neurological deterioration revealing adult polyglucosan body disease J Neurol Sci, 2012 ; 324 (1-2) : 179-182
