K. Bürk
Department of Neurology
University of Tübingen
Germany
Name/email consistency: high
- MRI-based volumetric differentiation of sporadic cerebellar ataxia. Burk, K., Globas, C., Wahl, T., Bühring, U., Dietz, K., Zuhlke, C., Luft, A., Schulz, J.B., Voigt, K., Dichgans, J. Brain (2004)
- Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred. Bürk, K., Zühlke, C., König, I.R., Ziegler, A., Schwinger, E., Globas, C., Dichgans, J., Hellenbroich, Y. Neurology (2004)
- Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3. Bürk, K., Globas, C., Bösch, S., Klockgether, T., Zühlke, C., Daum, I., Dichgans, J. J. Neurol. (2003)
- Sporadic cerebellar ataxia associated with gluten sensitivity. Bürk, K., Bösch, S., Müller, C.A., Melms, A., Zühlke, C., Stern, M., Besenthal, I., Skalej, M., Ruck, P., Ferber, S., Klockgether, T., Dichgans, J. Brain (2001)
- Pontine MRI hyperintensities ("the cross sign") are not pathognomonic for multiple system atrophy (MSA). Bürk, K., Skalej, M., Dichgans, J. Mov. Disord. (2001)
- Executive dysfunction in spinocerebellar ataxia type 1. Bürk, K., Bösch, S., Globas, C., Zühlke, C., Daum, I., Klockgether, T., Dichgans, J. Eur. Neurol. (2001)
- Cognitive deficits in spinocerebellar ataxia 2. Bürk, K., Globas, C., Bösch, S., Gräber, S., Abele, M., Brice, A., Dichgans, J., Daum, I., Klockgether, T. Brain (1999)
- Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3. Bürk, K., Fetter, M., Abele, M., Laccone, F., Brice, A., Dichgans, J., Klockgether, T. J. Neurol. (1999)
