Items where Author is "Voermans, N."
Jump to: 2015 Number of items: 2. 2015Kraeva, N. and Heytens, L. and Jungbluth, H. and Treves, S. and Voermans, N. and Kamsteeg, C. and Ceuterick-de Groote, C. and Baets, J. and Riaz, S.. (2015) Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy. Neuromuscular Disorders, 25 (7). pp. 567-576. Snoek, M. and van Engelen, B. G. M. and Küsters, B. and Lammens, M. and Meijer, R. and Molenaar, J. P. F. and Raaphorst, J. and Verschuuren-Bemelmans, C. C. and Straathof, C. S. M. and Sie, L. T. L. and de Coo, I. F. and van der Pol, W. L. and de Visser, M. and Scheffer, H. and Treves, S. and Jungbluth, H. and Voermans, N. and Kamsteef, E.-J.. (2015) RYR1‐related myopathies: a wide spectrum of phenotypes throughout life. European Journal of Neurology, 22 (7). pp. 1094-1112. |
