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21.
Ishikawa, K.* et al.: Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians. Neurology 77, 1853-1855 (2011)
22.
Schulte, E.C.* et al.: Variant screening of the coding regions of MEIS1 in patients with restless legs syndrome. Neurology 76, 1106-1108 (2011)
23.
Schlachter, K.* et al.: A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures. Neurology 72, 974-978 (2009)
24.
Winkelmann, J. & Müller-Myhsok, B.*: Genetics of restless legs syndrome - A burning urge to move. Neurology 70, 664-665 (2008)
25.
Fernández-Santiago, R.* et al.: Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALS. Neurology 66, 1929-1931 (2006)
26.
Kamm, C.* et al.: Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia. Neurology 67, 1857-1859 (2006)
27.
Liebetanz, K.M.* et al.: RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity. Neurology 67, 320-321 (2006)
28.
Schulte, C.* et al.: Comprehensive association analysis of the NOS2A gene with Parkinson disease. Neurology 67, 2080-2082 (2006)
29.
Stogmann, E.* et al.: Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations. Neurology 67, 2029-2031 (2006)
30.
Hörtnagel, K. et al.: Infantile neuroaxonal dystrophy and pantothenate kinase-associated neurodegeneration: Locus heterogeneity. Neurology 63, 922-924 (2004)
31.
Riemenschneider, M.* et al.: Prion protein codon 129 polymorphism and risk of Alzheimer disease. Neurology 63, 364-366 (2004)
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