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Parkinsonism & Related Disorders|August 16, 2021
Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case seriesIvana Dzinovic, Matej Škorvánek, Ján Necpál, et al.
Cell Reports|October 26, 2018
KMT2B Is Selectively Required for Neuronal Transdifferentiation, and Its Loss Exposes Dystonia Candidate GenesGiulia Barbagiovanni, Pierre-Luc Germain, Michael Zech, et al.
American Journal of Human Genetics|November 15, 2016
Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized DystoniaMichael Zech, Sylvia Boesch, Esther M Maier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 14, 2010
Short-term attention and verbal fluency is decreased in restless legs syndrome patientsStephany Fulda, Marie E Beitinger, Simone Reppermund, et al.
BMC Health Services Research|October 28, 2021
The role of patient navigators in ambulatory care: overview of systematic reviewsHannah Budde, Gemma A Williams, Juliane Winkelmann, et al.
Sleep Medicine|November 1, 2003
Sleep and periodic limb movements in corticobasal degenerationThomas C Wetter, Hans Brunner, Victor Collado-Seidel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 24, 2017
Ferric carboxymaltose in patients with restless legs syndrome and nonanemic iron deficiency: A randomized trialClaudia Trenkwalder, Juliane Winkelmann, Wolfgang Oertel, et al.
Neurogenetics|August 30, 2017
Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencingMichael Zech, Robert Jech, Matias Wagner, et al.
Parkinsonism & Related Disorders|March 20, 2022
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonismBarbara Garavaglia, Sadeq Vallian, Luigi M Romito, et al.
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