The anatomical basis of dystonia: Current view using neuroimaging von Lehéricy, Stéphane, Tijssen, Marina A.J., Vidailhet, Marie, Kaji, Ryuji, Meunier, Sabine

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Familial adult myoclonus epilepsy: Neurophysiological investigations von Dubbioso, Raffaele, Suppa, Antonio, Tijssen, Marina A. J., Ikeda, Akio

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WDR45, one gene associated with multiple neurodevelopmental disorders von Cong, Yingying, So, Vincent, Tijssen, Marina A. J., Verbeek, Dineke S., Reggiori, Fulvio, Mauthe, Mario

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Substantiating the Short Burst Duration in Cortical Myoclonus von Veen, Sterre, Maliepaard, Amber, Stouwe, Madelein, Dalenberg, Jelle, Tuitert, Inge, Elting, Jan Willem J., Tijssen, Marina A.J.

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Negative Myoclonus: Neurophysiological Study and Clinical Impact in Progressive Myoclonus Ataxia von Pollini, Luca, Veen, Sterre, Elting, Jan Willem J., Tijssen, Marina A.J.

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Nomenclature of Genetically Determined Myoclonus Syndromes: Recommendations of the International Parkinson and Movement Disorder Society Task Force von Veen, Sterre, Zutt, Rodi, Klein, Christine, Marras, Connie, Berkovic, Samuel F., Caviness, John N., Shibasaki, Hiroshi, Koning, Tom J., Tijssen, Marina A.J.

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Clinical decision-making in functional and hyperkinetic movement disorders von van der Salm, Sandra M.A., van Rootselaar, Anne-Fleur, Cath, Daniëlle C., de Haan, Rob J., Koelman, Johannes H.T.M., Tijssen, Marina A.J.

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Electrophysiologic testing aids diagnosis and subtyping of myoclonus von Zutt, Rodi, Elting, Jan W, van Zijl, Jonathan C, van der Hoeven, J Han, Roosendaal, Christiaan M, Gelauff, Jeannette M, Peall, Kathryn J, Tijssen, Marina A.J

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Bilateral Pallidotomy for Dystonia: A Systematic Review von Centen, Liesanne M., Oterdoom, D.L. Marinus, Tijssen, Marina A.J., Lesman‐Leegte, Ivon, Egmond, Martje E., Dijk, J. Marc C.

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Moving on with (social) cognition in idiopathic cervical dystonia von Coenen, Maraike A, Spikman, Jacoba M, Smit, Marenka, Klooster, Jesper, Tijssen, Marina A J, Gerritsen, Marleen J J

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Teaching Video NeuroImages: The “round the houses” sign as a clinical clue for Niemann-Pick disease type C von Eggink, Hendriekje, Brandsma, Rick, van der Hoeven, Johannes H, Lange, Fiete, de Koning, Tom J, Tijssen, Marina A.J

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Natural Course of Myoclonus‐Dystonia in Adulthood: Stable Motor Signs But Increased Psychiatry von Timmers, Elze R., Peall, Kathryn J., Dijk, Joke M., Zutt, Rodi, Tijssen, Cees C., Bergmans, Bruno, Foncke, Elisabeth M., Tijssen, Marina A.J.

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A Gain‐of‐Function Variant in Dopamine D2 Receptor and Progressive Chorea and Dystonia Phenotype von Weijden, Marlous C.M., Rodriguez‐Contreras, Dayana, Delnooz, Cathérine C.S., Robinson, Brooks G., Condon, Alec F., Kielhold, Michelle L., Stormezand, Gilles N., Ma, Kai Yu, Dufke, Claudia, Williams, John T., Neve, Kim A., Tijssen, Marina A.J., Verbeek, Dineke S.

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Daily fluctuations of negative affect are only weakly associated with tremor symptoms in functional and organic tremor patients von Kramer, Gerrit, Bos, Elisabeth H., Edwards, Mark J., Tijssen, Marina A.J., Rosmalen, Judith G.M.

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Movement Disorders on YouTube — Caveat Spectator von Stamelou, Maria, Fung, Victor S.C, Bhatia, Kailash P, Tijssen, Marina A.J, Espay, Alberto J, Lang, Anthony E, Hallett, Mark, Edwards, Mark J

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Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene von Lohmann, Katja, Wilcox, Robert A., Winkler, Susen, Ramirez, Alfredo, Rakovic, Aleksandar, Park, Jin-Sung, Arns, Björn, Lohnau, Thora, Groen, Justus, Kasten, Meike, Brüggemann, Norbert, Hagenah, Johann, Schmidt, Alexander, Kaiser, Frank J., Kumar, Kishore R., Zschiedrich, Katja, Alvarez-Fischer, Daniel, Altenmüller, Eckart, Ferbert, Andreas, Lang, Anthony E., Münchau, Alexander, Kostic, Vladimir, Simonyan, Kristina, Agzarian, Marc, Ozelius, Laurie J., Langeveld, Antonius P. M., Sue, Carolyn M., Tijssen, Marina A. J., Klein, Christine

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Management of patients with myoclonus: available therapies and the need for an evidence-based approach von Dijk, Joke M, MD, Tijssen, Marina AJ, Dr

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Propriospinal myoclonus: Clinical reappraisal and review of literature von van der Salm, Sandra M.A, Erro, Roberto, Cordivari, Carla, Edwards, Mark J, Koelman, Johannes H.T.M, Ende, Tom van den, Bhatia, Kailash P, van Rootselaar, Anne-Fleur, Brown, Peter, Tijssen, Marina A.J

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Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update von Lange, Lara M., Gonzalez‐Latapi, Paulina, Rajalingam, Rajasumi, Tijssen, Marina A.J., Ebrahimi‐Fakhari, Darius, Gabbert, Carolin, Ganos, Christos, Ghosh, Rhia, Kumar, Kishore R., Lang, Anthony E., Rossi, Malco, Veen, Sterre, Warrenburg, Bart, Warner, Tom, Lohmann, Katja, Klein, Christine, Marras, Connie

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Reply to: “Childhood Onset Chorea Caused by a Recurrent De Novo DRD2 Variant” von Weijden, Marlous C.M., Rodriguez‐Contreras, Dayana, Neve, Kim A., Verbeek, Dineke S., Tijssen, Marina A.J.

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