Recent advances in the diagnosis, genetics and treatment of restless legs syndromeTRENKWALDER, Claudia; HÖGL, Birgit; WINKELMANN, Juliane et al.Journal of neurology. 2009, Vol 256, Num 4, pp 539-553, issn 0340-5354, 15 p.Article

Long-term course of Restless legs syndrome in dialysis patients after kidney transplantationWINKELMANN, Juliane; STAUTNER, Anette; SAMTLEBEN, Walter et al.Movement disorders. 2002, Vol 17, Num 5, pp 1072-1076, issn 0885-3185Article

When Parkinson's disease patients go to sleep: specific sleep disturbances related to Parkinson's diseaseSCHULTE, Eva C; WINKELMANN, Juliane.Journal of neurology. Supplement. 2011, Vol 258, Num 2, issn 0939-1517, S328-S335Conference Paper

Assessment of spontaneously occurring periodic limb movements in sleep in the ratBAIER, Paul Christian; WINKELMANN, Juliane; HÖHNE, Arnold et al.Journal of the neurological sciences. 2002, Vol 198, Num 1-2, pp 71-77, issn 0022-510XArticle

The restless legs syndrome: A genetic view of the diseaseWINKELMANN, Juliane; ECKARD, Karin; MÜLLER-MYSHOK, Bertram et al.Somnologie (Berlin. Print). 2002, Vol 6, Num 1, pp 3-6, issn 1432-9123Article

Short-Term Attention and Verbal Fluency is Decreased in Restless Legs Syndrome PatientsFULDA, Stephany; BEITINGER, Marie E; REPPERMUND, Simone et al.Movement disorders. 2010, Vol 25, Num 15, pp 2641-2648, issn 0885-3185, 8 p.Article

Myoclonus-Dystonia in 18p Deletion SyndromeKOWARIK, Markus C; LANGER, Sabine; KERI, Corinna et al.Movement disorders. 2011, Vol 26, Num 3, pp 560-561, issn 0885-3185, 2 p.Article

Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13KEMLINK, David; PLAZZI, Giuseppe; FRAUSCHER, Birgit et al.Neurogenetics (Oxford. Print). 2008, Vol 9, Num 2, pp 75-82, issn 1364-6745, 8 p.Article

Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorderBADHWAR, Amanpreet; BERKOVIC, Samuel F; RIVEST, Jean et al.Brain. 2004, Vol 127, pp 2173-2182, issn 0006-8950, 10 p., 10Article

Narcolepsy is a common phenotype in HSAN IE and ADCA-DNMOGHADAM, Keivan Kaveh; PIZZA, Fabio; DONADIO, Vincenzo et al.Brain. 2014, Vol 137, pp 1643-1655, issn 0006-8950, 13 p., 6Article

A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson DiseaseZIMPRICH, Alexander; BENET-PAGES, Anna; ROSSLE, Shaila C et al.American journal of human genetics. 2011, Vol 89, Num 1, pp 168-175, issn 0002-9297, 8 p.Article

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndromeSCHORMAIR, Barbara; KEMLINK, David; OERTEL, Wolfgang et al.Nature genetics. 2008, Vol 40, Num 8, pp 946-948, issn 1061-4036, 3 p.Article

Variants in the Neuronal Nitric Oxide Synthase (nNOS, NOS1) Gene are Associated with Restless Legs SyndromeWINKELMANN, Juliane; LICHTNER, Peter; ILLIG, Thomas et al.Movement disorders. 2008, Vol 23, Num 3, pp 350-358, issn 0885-3185, 9 p.Article

Narcolepsy is strongly associated with the T-cell receptor alpha locusHALLMAYER, Joachim; FARACO, Juliette; HONG, Sheng Seung-Chul et al.Nature genetics. 2009, Vol 41, Num 6, pp 708-711, issn 1061-4036, 4 p.Article

Heritability of Sleep ElectroencephalogramAMBROSIUS, Urte; LIETZENMAIER, Sonja; WEHRLE, Renate et al.Biological psychiatry (1969). 2008, Vol 64, Num 4, pp 344-348, issn 0006-3223, 5 p.Article

Animal Studies in Restless Legs SyndromeBAIER, Paul Christian; ONDO, William G; WINKELMANN, Juliane et al.Movement disorders. 2007, Vol 22, issn 0885-3185, S459-S465, SUP18Article

Clinical Trials in Restless Legs Syndrome : Recommendations of the European RLS Study Group (EURLSSG)TRENKWALDER, Claudia; KOHNEN, Ralf; KLEIN, Christine et al.Movement disorders. 2007, Vol 22, issn 0885-3185, S495-S504, SUP18Article

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsyWINKELMANN, Juliane; LING LIN; POLI, Francesca et al.Human molecular genetics (Print). 2012, Vol 21, Num 10, pp 2205-2210, issn 0964-6906, 6 p.Article

MEIS 1 and BTBD9: genetic association with restless leg syndrome in end stage renal diseaseSCHORMAIR, Barbara; PLAG, Jens; DARDIOTIS, Efthimios et al.Journal of medical genetics. 2011, Vol 48, Num 7, pp 462-466, issn 0022-2593, 5 p.Article

Parkinson's disease risk score: moving to a premotor diagnosisWINKLER, Jiirgen; EHRET, Reinhard; BÜTTNER, Thomas et al.Journal of neurology. Supplement. 2011, Vol 258, Num 2, issn 0939-1517, S311-S315Conference Paper

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regionsWINKELMANN, Juliane; SCHORMAIR, Barbara; TRENKWALDER, Claudia et al.Nature genetics. 2007, Vol 39, Num 8, pp 1000-1006, issn 1061-4036, 7 p.Article

Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndromeWINKELMANN, Juliane; LICHTNER, Peter; PÜTZ, Benno et al.Movement disorders. 2006, Vol 21, Num 1, pp 28-33, issn 0885-3185, 6 p.Article

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's diseaseSCHULTE, Eva C; MOLLENHAUER, Brit; GIEGER, Christian et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 3, pp 281-285, issn 1364-6745, 5 p.Article

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levelsOEXLE, Konrad; RIED, Janina S; ILLIG, Thomas et al.Human molecular genetics (Print). 2011, Vol 20, Num 5, pp 1042-1047, issn 0964-6906, 6 p.Article

Family-based association study of the restless legs syndrome loci 2 and 3 in a European PopulationKEMLINK, David; POLO, Olli; FRAUSCHER, Birgit et al.Movement disorders. 2007, Vol 22, Num 2, pp 207-212, issn 0885-3185, 6 p.Article