Publications (1184)

Lommel, M., Cirak, S., Willer, T., Hermann, R., Uyanik, G., van Bokhoven, H., Korner, C., Voit, T., Baric, I., Hehr, U., Strahl, S. :
Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathies Neurology, 2010 ; 74 (2) : 157-64
Van den Bergh, P. Y., Hadden, R. D., Bouche, P., Cornblath, D. R., Hahn, A., Illa, I., Koski, C. L., Leger, J. M., Nobile-Orazio, E., Pollard, J., Sommer, C., van Doorn, P. A., van Schaik, I. N. :
European Federation of Neurological Societies/Peripheral Nerve Society Guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society – First Revision Journal of the Peripheral Nervous System, 2010 ; 15 (1) : 1-9
Azzabou, N., Paragios, N., Guichard, F. :
Image reconstruction using particle filters and multiple hypotheses testing IEEE Trans Image Process, 2010 ; 19 (5) : 1181-90
Belus, A., Piroddi, N., Ferrantini, C., Tesi, C., Cazorla, O., Toniolo, L., Drost, M., Mearini, G., Carrier, L., Rossi, A., Mugelli, A., Cerbai, E., van der Velden, J., Poggesi, C. :
Effects of Chronic Atrial Fibrillation on Active and Passive Force Generation in Human Atrial Myofibrils Circ Res, 2010 ; 107 (1) : 144-152
Gant Luxton, G W, Gomes, E. R., Folker, E S, Vintinner, E, Gundersen, G. G. :
Linear arrays of nuclear envelope proteins harness retrograde actin flow for nuclear movement Science, 2010 ; 329 (5994) : 956-959
Mouisel, E., Vignaud, A., Hourde, C., Butler-Browne, G., Ferry, A. :
Muscle weakness and atrophy are associated with decreased regenerative capacity and changes in mTOR signaling in skeletal muscles of venerable (18-24-month-old) dystrophic mdx mice Muscle Nerve, 2010 ; 41 (6) : 809-818
Zuckerman, N. S., Howard, W. A., Bismuth, J., Gibson, K., Edelman, H., Berrih-Aknin, S., Dunn-Walters, D., Mehr, R. :
Ectopic GC in the thymus of myasthenia gravis patients show characteristics of normal GC Eur J Immunol, 2010 ; 40 (4) : 1150-61
Carrier, L, Schlossarek, S, Willis, M, Eschenhagen, T :
Ubiquitin-proteasome system nonsense-mediated mRNA decay in hypertrophic cardiomyopathy Cardiovasc Res, 2010 ; 85 (2) : 330-338
Knoblauch, H., Geier, C., Adams, S., Budde, B., Rudolph, A., Zacharias, U., Schulz-Menger, J., Spuler, A., Ben Yaou, R., Nurnberg, P., Voit, T., Bonne, G., Spuler, S. :
Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation Ann Neurol, 2010 ; 67 (1) : 136-40
Schessl, J., Columbus, A., Hu, Y., Zou, Y., Voit, T., Goebel, H. H., Bonnemann, C. G. :
Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1 Neuropediatrics, 2010 ; 41 (1) : 43-6