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10 Records found.
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1.
Bartl, M.* ; Winkelmann, J. ; Högl, B.* ; Paulus, W.* & Trenkwalder, C.*: Frequent neurological diseases associated with the restless legs syndrome. Nervenarzt 89, 1156-1164 (2018)
2.
Schormair, B. et al.: Identification of novel risk loci for restless legs syndrome: A meta-analysis of genome-wide association studies in individuals of European ancestry: A meta-analysis. Lancet Neurol. 16, 898–907 (2017)
3.
Trenkwalder, C.* ; Allen, R.P.* ; Högl, B.* ; Paulus, W.* & Winkelmann, J.: Restless legs syndrome associated with major diseases: A systematic review and new concept. Neurology 86, 1336-1343 (2016)
4.
Schulte, E.C. et al.: Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. PLoS ONE 9:e98092 (2014)
5.
Winkelmann, J. et al.: Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. PLoS Genet. 7:e1002171 (2011)
6.
Schormair, B. et al.: PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nat. Genet. 40, 946-948 (2008)
7.
Winkelmann, J. et al.: Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. Mov. Disord. 23, 350-358 (2008)
8.
García-Borreguero, D.* et al.: Augmentation as a treatment complication of restless legs syndrome: Concept and management. Mov. Disord. 22, (Suppl.18), 476-484 (2007)
9.
García-Borreguero, D.* et al.: Diagnostic standards for dopaminergic augmentation of restless legs syndrome: Report from a World Association of Sleep Medicine-International Restless Legs Syndrome Study Group consensus conference at the Max Planck Institute. Sleep Med. 8, 520-530 (2007)
10.
Winkelmann, J. et al.: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat. Genet. 39, 1000-1006 (2007)