Publications (1181)

Hervier, B., Lambert, M., Hachulla, E., Musset, L., Benveniste, O., Piette, J. C., Amoura, Z., Costedoat-Chalumeau, N. :
Anti-synthetase syndrome positive for anti-isoleucyl-tRNA synthetase antibodies: an unusual case overlapping with systemic sclerosis and Sjogren’s syndrome Rheumatology (Oxford), 2011 ; 50 (6) : 1175-6
Monteilhet, V., Saheb, S., Boutin, S., Leborgne, C., Veron, P., Montus, M. F., Moullier, P., Benveniste, O., Masurier, C. :
A 10 Patient Case Report on the Impact of Plasmapheresis Upon Neutralizing Factors Against Adeno-associated Virus (AAV) Types 1, 2, 6, and 8 Mol Ther, 2011 ; 19 (11) : 2084-91
Charrier, S., Ferrand, M., Zerbato, M., Precigout, G., Viornery, A., Bucher-Laurent, S., Benkhelifa-Ziyyat, S., Merten, O. W., Perea, J., Galy, A. :
Quantification of lentiviral vector copy numbers in individual hematopoietic colony-forming cells shows vector dose-dependent effects on the frequency and level of transduction Gene Ther, 2011 ; 18 (5) : 479-87
Koutsoulidou, A., Mastroyiannopoulos, N. P., Furling, D., Uney, J. B., Phylactou, L. A. :
Endogenous TWIST expression and differentiation are opposite during human muscle development Muscle Nerve, 2011 ; 44 (6) : 984-6
Romero, N. B., Bitoun, M. :
Centronuclear myopathies Semin Pediatr Neurol, 2011 ; 18 (4) : 250-6
Baraibar, M. A., Hyzewicz, J., Rogowska-Wresinska, A., Ladouce, R., Roepstorff, P., Mouly, V., Friguet, B. :
Oxidative stress-induced proteome alterations target different cellular pathways in human myoblasts Free Radic Biol Med, 2011 ; 51 (8) : 1522-1532
Forsha, D., Li, J. S., Smith, P. B., van der Ploeg, A. T., Kishnani, P., Pasquali, S. K., Laforet, P :
Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy Genet Med, 2011 ; 13 (7) : 625-631
Mayeuf, A., Relaix, F. :
La voie Notch – Du developpement a la regeneration du muscle squelettique. Med Sci (Paris), 2011 ; 27 (5) : 521-526
Vieitez, I., Teijeira, S., Fernandez, J. M., San Millan, B., Miranda, S., Ortolano, S., Louis, S., Laforet, P., Navarro, C. :
Molecular and clinical study of McArdle’s disease in a cohort of 123 European patients. Identification of 20 novel mutations Neuromuscul Disord, 2011 ; 21 (12) : 817-823
Besson, V., Smeriglio, P., Wegener, A., Relaix, F., Oumesmar, B. N., Sassoon, D. A., Marazzi, G. :
PW1 gene/paternally expressed gene 3 (PW1/Peg3) identifies multiple adult stem and progenitor cell populations Proc Natl Acad Sci U S A, 2011 ; 108 (28) : 11470-5