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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)
Wang, L.* et al.: Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: Analysis of a large multicenter study. Neurobiol. Aging 49, 217.e1-217.e4 (2017)
García-Borreguero, D.* et al.: Guidelines for the first-line treatment of restless legs syndrome/Willis-Ekbom disease, prevention and treatment of dopaminergic augmentation: A combined task force of the IRLSSG, EURLSSG, and the RLS-foundation. Sleep Med. 21, 1-11 (2016)
Wang, L.* et al.: Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. Neurology 85, 1283-1292 (2015)
Sharma, M.* et al.: A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. J. Med. Genet. 49, 721-726 (2012)
Sharma, M.L.* et al.: Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 79, 659-667 (2012)
Schormair, B. et al.: MEIS1 and BTBD9: Genetic association with restless leg syndrome in end stage renal disease. J. Med. Genet. 48, 462-466 (2011)
Kemlink, D. et al.: Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13. Neurogenetics 9, 75-82 (2008)
Kemlink, D. et al.: Family-based association study of the restless legs syndrome loci 2 and 3 in a European population. Mov. Disord. 22, 207-212 (2007)
Winkelmann, J. et al.: Genetics of restless legs syndrome (RLS: State-of-the-art and future directions). Mov. Disord. 22, (Suppl.18), 449-458 (2007)