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Annals of Clinical and Translational Neurology|May 27, 2026
Prominent Movement Disorders in RNU2-2-Related SpliceosomopathyMagdalena Krygier, Ugo Sorrentino, Matias Wagner, et al.
European Journal of Ageing|July 1, 2016
Predictors of social leisure activities in older Europeans with and without multimorbidityHenrike Galenkamp, Cristina Gagliardi, Andrea Principi, et al.
The Lancet. Neurology|October 22, 2013
Prolonged release oxycodone-naloxone for treatment of severe restless legs syndrome after failure of previous treatment: a double-blind, randomised, placebo-controlled trial with an open-label extensionClaudia Trenkwalder, Heike Beneš, Ludger Grote, et al.
Neuropediatrics|March 28, 2024
Genome Sequencing for Cases Unsolved by Exome Sequencing: Identifying a Single-Exon Deletion in TBCK in a Case from 30 Years AgoMaureen Jacob, Melanie Brugger, Stephanie Andres, et al.
Case Reports in Neurological Medicine|March 9, 2026
Mixed Movement Disorder Caused by ADCY5 Pathogenic Variant Successfully Treated With Caffeine: A Case From UkraineEugenia Tsoma, Taras Studeniak, Robert Jech, et al.
Plants (Basel, Switzerland)|July 19, 2019
Phenolic Compounds as Unambiguous Chemical Markers for the Identification of Keystone Plant Species in the Bale Mountains, EthiopiaBruk Lemma, Claudius Grehl, Michael Zech, et al.
Brain : a Journal of Neurology|September 30, 2021
Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onsetNazanin Mirza-Schreiber, Michael Zech, Rory Wilson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2023
ATP2B2 de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizuresElena Poggio, Lucia Barazzuol, Andrea Salmaso, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation DysfunctionPhilip Harrer, Matej Škorvánek, Volker Kittke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2013
Mitochondrial membrane protein associated neurodegenration: a novel variant of neurodegeneration with brain iron accumulationEva C Schulte, Malte C Claussen, Angela Jochim, et al.
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