Identification of genetic causes of restless legs syndrome

Lohmann, Katja (Principal Investigator (PI))
Stephani, Ulrich (Principal Investigator (PI))
Klein, Christine (Associated Staff)

Institute of Neurogenetics

University of Kiel

Project: DFG Projects › DFG Individual Projects

5 Journal articles

5 results

2008
Childhood-onset restless Legs syndrome: Clinical and genetic features of 22 families
Muhle, H., Neumann, A., Lohmann-Hedrich, K., Lohnau, T., Lu, Y., Winkler, S., Waltz, S., Fischenbeck, A., Kramer, P. L., Klein, C. & Stephani, U., 15.06.2008, In: Movement Disorders. 23, 8, p. 1113-1121 9 p.
Research output: Journal Articles › Journal articles › Research › peer-review
43 Citations (Scopus)
Evidence for linkage of restless legs syndrome to chromosome 9p: Are there two distinct loci?
Lohmann-Hedrich, K., Neumann, A., Kleensang, A., Lohnau, T., Muhle, H., Djarmati, A., König, I. R., Pramstaller, P. P., Schwinger, E., Kramer, P. L., Ziegler, A., Stephani, U. & Klein, C., 01.01.2008, In: Neurology. 70, 9, p. 686-694 9 p.
Research output: Journal Articles › Journal articles › Research › peer-review
33 Citations (Scopus)
2007
Clinical trials in restless legs syndrome - Recommendations of the European RLS Study Group (EURLSSG)
Trenkwalder, C., Kohnen, R., Allen, R. P., Beneš, H., Ferini-Strambi, L., Garcia-Borreguero, D., Hadjigeorgiou, G. M., Happe, S., Högl, B., Hornyak, M., Klein, C., Nass, A., Montagna, P., Oertel, W. H., O'Keeffe, S., Paulus, W., Poewe, W., Provini, F., Pramstaller, P. P. & Sieminski, M. & 6 others, Sonka, K., Stiasny-Kolster, K., De Weerd, A., Wetter, T. C., Winkelmann, J. & Zucconi, M., 01.12.2007, In: Movement Disorders. 22, SUPPL. 18
Research output: Journal Articles › Journal articles › Research › peer-review
20 Citations (Scopus)
Family-based association study of the restless legs syndrome loci 2 and 3 in a European population
Kemlink, D., Polo, O., Montagna, P., Provini, F., Stiasny-Kolster, K., Oertel, W., De Weerd, A., Nevsimalova, S., Sonka, K., Högl, B., Frauscher, B., Poewe, W., Trenkwalder, C., Pramstaller, P. P., Ferini-Strambi, L., Zucconi, M., Konofal, E., Arnulf, I., Hadjigeorgiou, G. M. & Happe, S. & 6 others, Klein, C., Hiller, A., Lichtner, P., Meitinger, T., Müller-Myshok, B. & Winkelmann, J., 15.01.2007, In: Movement Disorders. 22, 2, p. 207-212 6 p.
Research output: Journal Articles › Journal articles › Research › peer-review
24 Citations (Scopus)
Genetics of restless legs syndrome (RLS): State-of-the-art and future directions
Winkelmann, J., Polo, O., Provini, F., Nevsimalova, S., Kemlink, D., Sonka, K., Högl, B., Poewe, W., Stiasny-Kolster, K., Oertel, W., De Weerd, A., Strambi, L. F., Zucconi, M., Pramstaller, P. P., Arnulf, I., Trenkwalder, C., Klein, C., Hadjigeorgiou, G. M., Happe, S. & Rye, D. & 1 others, Montagna, P., 01.12.2007, In: Movement Disorders. 22, SUPPL. 18
Research output: Journal Articles › Journal articles › Research › peer-review
63 Citations (Scopus)

Identification of genetic causes of restless legs syndrome

Research Output

Search results

Childhood-onset restless Legs syndrome: Clinical and genetic features of 22 families

Evidence for linkage of restless legs syndrome to chromosome 9p: Are there two distinct loci?

Clinical trials in restless legs syndrome - Recommendations of the European RLS Study Group (EURLSSG)

Family-based association study of the restless legs syndrome loci 2 and 3 in a European population

Genetics of restless legs syndrome (RLS): State-of-the-art and future directions