Items where Author is "Pillay, K."

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.

2008

Viale, G. and Regan, M. M. and Maiorano, E. and Mastropasqua, M. G. and Golouh, R. and Perin, T. and Brown, R. W. and Kovács, A. and Pillay, K. and Öhlschlegel, C. and Braye, S. and Grigolato, P. and Rusca, T. and Gelber, R. D. and Castiglione-Gertsch, M. and Price, K. N. and Goldhirsch, A. and Gusterson, B. A. and Coates, A. S.. (2008) Chemoendocrine compared with endocrine adjuvant therapies for node-negative breast cancer : predictive value of centrally reviewed expression of estrogen and progesterone receptors, international breast cancer study group. Journal of clinical oncology, Vol. 9. pp. 1404-1410.