Items where Author is "Peyer, A. K."
Jump to: 2013 Number of items: 2. 2013Peyer, A. K. and Kinter, J. and Hench, J. and Frank, S. and Fuhr, P. and Thomann, S. and Fischmann, A. and Kneifel, S. and Camano, P. and Munain, A. L. and Sinnreich, M. and Renaud, S.. (2013) Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia. Neuromuscular disorders, Vol. 23, H. 2. pp. 149-154. Peyer, A. K. and Abicht, A. and Heinimann, K. and Sinnreich, M. and Fischer, D.. (2013) Quinine sulfate as a therapeutic option in a patient with slow channel congenital myasthenic syndrome. Neuromuscular disorders, Vol. 23, H. 7. pp. 571-574. |
