Cerebellar rTMS and PAS effectively induce cerebellar plasticity von Pauly, Martje G., Steinmeier, Annika, Bolte, Christina, Hamami, Feline, Tzvi, Elinor, Münchau, Alexander, Bäumer, Tobias, Weissbach, Anne

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Not to Miss: Intronic Variants, Treatment, and Review of the Phenotypic Spectrum in VPS13D -Related Disorder von Pauly, Martje G, Brüggemann, Norbert, Efthymiou, Stephanie, Grözinger, Anne, Diaw, Sokhna Haissatou, Chelban, Viorica, Turchetti, Valentina, Vona, Barbara, Tadic, Vera, Houlden, Henry, Münchau, Alexander, Lohmann, Katja

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Cerebellar transcranial current stimulation – An intraindividual comparison of different techniques von Herzog, Rebecca, Berger, Till M., Pauly, Martje G., Xue, Honghu, Rueckert, Elmar, Münchau, Alexander, Bäumer, Tobias, Weissbach, Anne

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Time estimation and arousal responses in dopa-responsive dystonia von Becker, Leonie F., Tunc, Sinem, Murphy, Peter, Bäumer, Tobias, Weissbach, Anne, Pauly, Martje G., Al-Shorafat, Duha M., Saranza, Gerard, Lang, Anthony E., Beste, Christian, Donner, Tobias H., Verrel, Julius, Münchau, Alexander

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Somatosensory-motor cortex interactions measured using dual-site transcranial magnetic stimulation von Brown, Matt J.N., Weissbach, Anne, Pauly, Martje G., Vesia, Michael, Gunraj, Carolyn, Baarbé, Julianne, Münchau, Alexander, Bäumer, Tobias, Chen, Robert

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Plasmid-Based Generation of Induced Neural Stem Cells from Adult Human Fibroblasts von Capetian, Philipp, Azmitia, Luis, Pauly, Martje G, Krajka, Victor, Stengel, Felix, Bernhardi, Eva-Maria, Klett, Mariana, Meier, Britta, Seibler, Philip, Stanslowsky, Nancy, Moser, Andreas, Knopp, Andreas, Gillessen-Kaesbach, Gabriele, Nikkhah, Guido, Wegner, Florian, Döbrössy, Máté, Klein, Christine

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Adherent vs. Free-Floating Neural Induction by Dual SMAD Inhibition for Neurosphere Cultures Derived from Human Induced Pluripotent Stem Cells von Pauly, Martje G, Krajka, Victor, Stengel, Felix, Seibler, Philip, Klein, Christine, Capetian, Philipp

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Ventral Telencephalic Patterning Protocols for Induced Pluripotent Stem Cells von Krajka, Victor, Naujock, Maximilian, Pauly, Martje G., Stengel, Felix, Meier, Britta, Stanslowsky, Nancy, Klein, Christine, Seibler, Philip, Wegner, Florian, Capetian, Philipp

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Repeat length in spinocerebellar ataxia type 4 (SCA4) predicts age at onset and disease severity von Dalski, Andreas, Pauly, Martje G., Hanssen, Henrike, Hagenah, Johann, Hellenbroich, Yorck, Schmidt, Christian, Strohschehn, Jassemien, Spielmann, Malte, Zühlke, Christine, Brüggemann, Norbert

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Relationship of Genotype, Phenotype, and Treatment in Dopa‐Responsive Dystonia: MDSGene Review von Weissbach, Anne, Pauly, Martje G., Herzog, Rebecca, Hahn, Lisa, Halmans, Sara, Hamami, Feline, Bolte, Christina, Camargos, Sarah, Jeon, Beomseok, Kurian, Manju A., Opladen, Thomas, Brüggemann, Norbert, Huppertz, Hans‐Jürgen, König, Inke R., Klein, Christine, Lohmann, Katja

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Expanding Data Collection for the MDSGene Database: X‐linked Dystonia‐Parkinsonism as Use Case Example von Pauly, Martje G., Ruiz López, Marta, Westenberger, Ana, Saranza, Gerard, Brüggemann, Norbert, Weissbach, Anne, Rosales, Raymond L., Diesta, Cid C., Jamora, Roland D.G., Reyes, Charles J., Madoev, Harutyun, Petkovic, Sonja, Ozelius, Laurie J., Klein, Christine, Domingo, Aloysius

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NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia von Coutelier, Marie, Jacoupy, Maxime, Janer, Alexandre, Renaud, Flore, Auger, Nicolas, Saripella, Ganapathi-Varma, Ancien, François, Pucci, Fabrizio, Rooman, Marianne, Gilis, Dimitri, Larivière, Roxanne, Sgarioto, Nicolas, Valter, Rémi, Guillot-Noel, Léna, Le Ber, Isabelle, Sayah, Sabrina, Charles, Perrine, Nümann, Astrid, Pauly, Martje G, Helmchen, Christoph, Deininger, Natalie, Haack, Tobias B, Brais, Bernard, Brice, Alexis, Trégouët, David-Alexandre, El Hachimi, Khalid H, Shoubridge, Eric A, Durr, Alexandra, Stevanin, Giovanni

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De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia von Van de Vondel, Liedewei, De Winter, Jonathan, Beijer, Danique, Coarelli, Giulia, Wayand, Melanie, Palvadeau, Robin, Pauly, Martje G., Klein, Katrin, Rautenberg, Maren, Guillot‐Noël, Léna, Deconinck, Tine, Vural, Atay, Ertan, Sibel, Dogu, Okan, Uysal, Hilmi, Brankovic, Vesna, Herzog, Rebecca, Brice, Alexis, Durr, Alexandra, Klebe, Stephan, Stock, Friedrich, Bischoff, Almut Turid, Rattay, Tim W., Sobrido, María‐Jesús, De Michele, Giovanna, De Jonghe, Peter, Klopstock, Thomas, Lohmann, Katja, Zanni, Ginevra, Santorelli, Filippo M., Timmerman, Vincent, Haack, Tobias B., Züchner, Stephan, Schüle, Rebecca, Stevanin, Giovanni, Synofzik, Matthis, Basak, A. Nazli, Baets, Jonathan

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EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia von Kuipers, Demy J. S., Mandemakers, Wim, Lu, Chin‐Song, Olgiati, Simone, Breedveld, Guido J., Fevga, Christina, Tadic, Vera, Carecchio, Miryam, Osterman, Bradley, Sagi‐Dain, Lena, Wu‐Chou, Yah‐Huei, Chen, Chiung C., Chang, Hsiu‐Chen, Wu, Shey‐Lin, Yeh, Tu‐Hsueh, Weng, Yi‐Hsin, Elia, Antonio E., Panteghini, Celeste, Marotta, Nicolas, Pauly, Martje G., Kühn, Andrea A., Volkmann, Jens, Lace, Baiba, Meijer, Inge A., Kandaswamy, Krishna, Quadri, Marialuisa, Garavaglia, Barbara, Lohmann, Katja, Bauer, Peter, Mencacci, Niccolò E., Lubbe, Steven J., Klein, Christine, Bertoli‐Avella, Aida M., Bonifati, Vincenzo

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Subthalamic nucleus conditioning reduces premotor-motor interaction in Parkinson's disease von Pauly, Martje G., Barlage, Magdalena, Hamami, Feline, Steinhardt, Julia, Baarbé, Julianne, Tran, Stephanie, Hanssen, Henrike, Herzog, Rebecca, Tadic, Vera, Brüggemann, Norbert, Chen, Robert, Münchau, Alexander, Bäumer, Tobias, Weissbach, Anne

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Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes von Demidov, German, Laurie, Steven, Torella, Annalaura, Piluso, Giulio, Scala, Marcello, Morleo, Manuela, Nigro, Vincenzo, Graessner, Holm, Banka, Siddharth, Lohmann, Katja, Ossowski, Stephan

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Multimodal Longitudinal Neurophysiological Investigations in Dopa‐Responsive Dystonia von Weissbach, Anne, Steinmeier, Annika, Pauly, Martje G., Al‐Shorafat, Duha M., Saranza, Gerard, Lang, Anthony E., Brüggemann, Norbert, Tadic, Vera, Klein, Christine, Lohmann, Katja, Brown, Matt J.N., Beste, Christian, Münchau, Alexander, Bäumer, Tobias

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The Expanding Phenotypical Spectrum of WARS2 -Related Disorder: Four Novel Cases with a Common Recurrent Variant von Pauly, Martje G, Korenke, G Christoph, Diaw, Sokhna Haissatou, Grözinger, Anne, Cazurro-Gutiérrez, Ana, Pérez-Dueñas, Belén, González, Victoria, Macaya, Alfons, Serrano Antón, Ana Teresa, Peterlin, Borut, Božović, Ivana Babić, Maver, Aleš, Münchau, Alexander, Lohmann, Katja

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Severe Scratching in Spinocerebellar Ataxia 17: Another Case von Pauly, Martje G, Münchau, Alexander, Brüggemann, Norbert

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Compound Heterozygous DARS2 Mutations as a Mimic of Hereditary Spastic Paraplegia von Pauly, Martje G., Hellenbroich, Yorck, Grundmann‐Hauser, Kathrin, Hinrichs, Frauke, Lohmann, Katja, Brüggemann, Norbert

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