Items where Author is "Jungbluth, H."

2015

Rokach, O. and Sekulic-Jablanovi, M. and Voermans, N. and Wilmhurst, J. and Pillay, K. and Heytens, L. and Zhou, H. and Muntoni, F. and Gautel, M. and Nevo, Y. and Mitrani-Rosenbaum, S. and Attali, R. and Finotti, A. and Gambari, R. and Mosca, B. and Jungbluth, H. and Zorzato, F. and Treves, S.. (2015) Epigenetic changes as a common trigger of muscle weakness in congenital myopathies. Human Molecular Genetics, 24. pp. 4636-4647.

2013

Zhou, H. and Rokach, O. and Feng, L. and Munteanu, I. and Mamchaoui, K. and Wilmshurst, J. M. and Sewry, C. and Manzur, A. Y. and Pillay, K. and Mouly, V. and Duchen, M. and Jungbluth, H. and Treves, S. and Muntoni, F.. (2013) RyR1 Deficiency in Congenital Myopathies Disrupts Excitation–Contraction Coupling. Human Mutation, 34 (7). pp. 986-996.

2011

Treves, S. and Vukcevic, M. and Jeannet, P. Y. and Levano, S. and Girard, T. and Urwyler, A. and Fischer, D. and Voit, T. and Jungbluth, H. and Lillis, S. and Muntoni, F. and Quinlivan, R. and Sarkozy, A. and Bushby, K. and Zorzato, F.. (2011) Enhanced excitation-coupled Ca(2+) entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with central core disease. Human Molecular Genetics, 20 (3). pp. 589-600.