Items where Author is "Eymard, B."

2009

Huze, C. and Bauche, S. and Richard, P. and Chevessier, F. and Goillot, E. and Gaudon, K. and Ben Ammar, A. and Chaboud, A. and Grosjean, I. and Lecuyer, H. -A. and Bernard, V. and Rouche, A. and Alexandri, N. and Kuntzer, T. and Fardeau, M. and Fournier, E. and Brancaccio, A. and Ruegg, M. A. and Koenig, J. and Eymard, B. and Schaeffer, L. and Hantai, D.. (2009) Identification of an agrin mutation that causes congenital myasthenia and affects synapse function. American Journal of Human Genetics, 85 (2). pp. 155-167.

2008

Fischer, D. and Kley, R. A. and Strach, K. and Meyer, C. and Sommer, T. and Eger, K. and Rolfs, A. and Meyer, W. and Pou, A. and Pradas, J. and Heyer, C. M. and Grossmann, A. and Huebner, A. and Kress, W. and Reimann, J. and Schröder, R. and Eymard, B. and Fardeau, M. and Udd, B. and Goldfarb, L. and Vorgerd, M. and Olivé, M.. (2008) Distinct muscle imaging patterns in myofibrillar myopathies. Neurology, 71 (10). pp. 758-765.