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61.
Hopfner, F. et al.: The role of SCARB2 as susceptibility factor in Parkinson's disease. Mov. Disord. 28, 538-540 (2013)
62.
Schulte, E.C. et al.: Mitochondrial membrane protein associated neurodegeneration: A novel variant of neurodegeneration with brain iron accumulation. Mov. Disord. 28, 224-227 (2013)
63.
Fulda, S. ; Beitinger, M.E. ; Reppermund, S. ; Winkelmann, J. & Wetter, T.C.: Short-term attention and verbal fluency is decreased in restless legs syndrome patients. Mov. Disord. 25, 2641-2648 (2010)
64.
Kowarik, M.C.* et al.: Myoclonus-dystonia in 18p deletion syndrome. Mov. Disord. 26, 560-561 (2010)
65.
Lyoo, C.H.* et al.: Anticholinergic-responsive gait freezing in a patient with pantothenate kinase-associated neurodegeneration. Mov. Disord. 23, 283-284 (2008)
66.
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)
67.
Baier, P.C.* ; Ondo, W.G.* & Winkelmann, J.: Animal studies in restless legs syndrome. Mov. Disord. 22, (Suppl.18), 459-465 (2007)
68.
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)
69.
Haubenberger, D.* et al.: A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease. Mov. Disord. 22, 1640-1643 (2007)
70.
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)
71.
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)
72.
Vogl, F.D.* et al.: Restless legs syndrome: Epidemiological and clinicogenetic study in a South tyrolean population isolate. Mov. Disord. 21, 1189-1195 (2006)
73.
Winkelmann, J. et al.: Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. Mov. Disord. 21, 28-33 (2006)
74.
Antonini, A.* et al.: Genetic, clinical and imaging characterization of one patient with late-onset, slowly progressive, pantothenate kinase-associated neurodegeneration. Mov. Disord. 21, 417-425 (2005)
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