Christine Klein
Section of Clinical and Molecular Neurogenetics at the Department of Neurology
University of Lübeck
Lübeck
Germany
Name/email consistency: high
- A study of subtle motor signs in early Parkinson's disease. Schneider, S.A., Drude, L., Kasten, M., Klein, C., Hagenah, J. Mov. Disord. (2012)
- Progression of subtle motor signs in PINK1 mutation carriers with mild dopaminergic deficit. Eggers, C., Schmidt, A., Hagenah, J., Brüggemann, N., Klein, J.C., Tadic, V., Kertelge, L., Kasten, M., Binkofski, F., Siebner, H., Neumaier, B., Fink, G.R., Hilker, R., Klein, C. Neurology (2010)
- Hereditary parkinsonism: Parkinson disease look-alikes--an algorithm for clinicians to "PARK" genes and beyond. Klein, C., Schneider, S.A., Lang, A.E. Mov. Disord. (2009)
- Impact of recent genetic findings in Parkinson's disease. Klein, C., Lohmann-Hedrich, K. Curr. Opin. Neurol. (2007)
- Deciphering the role of heterozygous mutations in genes associated with parkinsonism. Klein, C., Lohmann-Hedrich, K., Rogaeva, E., Schlossmacher, M.G., Lang, A.E. Lancet. Neurol (2007)
- The genetics of Parkinson disease: Implications for neurological care. Klein, C., Schlossmacher, M.G. Nature Clinical Practice. Neurology (2006)
- PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism. Klein, C., Djarmati, A., Hedrich, K., Schäfer, N., Scaglione, C., Marchese, R., Kock, N., Schüle, B., Hiller, A., Lohnau, T., Winkler, S., Wiegers, K., Hering, R., Bauer, P., Riess, O., Abbruzzese, G., Martinelli, P., Pramstaller, P.P. Eur. J. Hum. Genet. (2005)