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Annals of Neurology|September 3, 2002
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset familiesJuliane Winkelmann, Bertram Muller-Myhsok, Hans-Ulrich Wittchen, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 7, 2007
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndromeJuliane Winkelmann, Peter Lichtner, Barbara Schormair, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 19, 2012
The LaLiMo Trial: lamotrigine compared with levetiracetam in the initial 26 weeks of monotherapy for focal and generalised epilepsy--an open-label, prospective, randomised controlled multicenter studyFelix Rosenow, Carmen Schade-Brittinger, Nicole Burchardi, et al.Nature Genetics|July 20, 2007
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regionsJuliane Winkelmann, Barbara Schormair, Peter Lichtner, et al.Pageof 2