Items where Author is "Voermans, Nicol"
Number of items: 3. 2017Treves, Susan and Jungbluth, Heinz and Voermans, Nicol and Muntoni, Francesco and Zorzato, Francesco. (2017) Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives. Seminars in Cell and Developmental Biology, 64. pp. 201-212. 2016Lopez, Rubén J. and Byrne, Susan and Vukcevic, Mirko and Sekulic-Jablanovic, Marijana and Xu, Lifen and Brink, Marijke and Alamelu, Jay and Voermans, Nicol and Snoeck, Marc and Clement, Emma and Muntoni, Francesco and Zhou, Haiyan and Radunovic, Aleksandar and Mohammed, Shehla and Wraige, Elizabeth and Zorzato, Francesco and Treves, Susan and Jungbluth, Heinz. (2016) An RYR1 mutation associated with malignant hyperthermia is also associated with bleeding abnormalities. Science Signaling, 9 (435). ra68. 2015Rokach, Ori and Sekulic-Jablanovic, Marijana and Voermans, Nicol and Wilmshurst, Jo and Pillay, Komala and Heytens, Luc and Zhou, Haiyan and Muntoni, Francesco and Gautel, Mathias and Nevo, Yoram and Mitrani-Rosenbaum, Stella and Attali, Ruben and Finotti, Alessia and Gambari, Roberto and Mosca, Barbara and Jungbluth, Heinz and Zorzato, Francesco and Treves, Susan. (2015) Epigenetic changes as a common trigger of muscle weakness in congenital myopathies. Human Molecular Genetics, 24 (16). pp. 4636-4647. |
