The preclinical stage of spinocerebellar ataxias von Maas, Roderick P.P.W.M, van Gaalen, Judith, Klockgether, Thomas, van de Warrenburg, Bart P.C

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The role of the cerebellum in degenerative ataxias and essential tremor: Insights from noninvasive modulation of cerebellar activity von Maas, Roderick P.P.W.M., Helmich, Rick C.G., Warrenburg, Bart P.C.

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Long-term treatment effect in cerebrotendinous xanthomatosis depends on age at treatment start von Stelten, Bianca M.L, Huidekoper, Hidde H, van de Warrenburg, Bart P.C, Brilstra, Eva H, Hollak, Carla E.M, Haak, Harm.R, Kluijtmans, Leo A.J, Wevers, Ron A, Verrips, Aad

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The genetic nomenclature of recessive cerebellar ataxias von Rossi, Malco, Anheim, Mathieu, Durr, Alexandra, Klein, Christine, Koenig, Michel, Synofzik, Matthis, Marras, Connie, van de Warrenburg, Bart P.

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The cerebellar cognitive affective syndrome scale reveals early neuropsychological deficits in SCA3 patients von Maas, Roderick P. P. W. M., Killaars, Sven, van de Warrenburg, Bart P. C., Schutter, Dennis J. L. G.

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Network localization of cervical dystonia based on causal brain lesions von Corp, Daniel T, Joutsa, Juho, Darby, R Ryan, Delnooz, Cathérine C S, van de Warrenburg, Bart P C, Cooke, Danielle, Prudente, Cecília N, Ren, Jianxun, Reich, Martin M, Batla, Amit, Bhatia, Kailash P, Jinnah, Hyder A, Liu, Hesheng, Fox, Michael D

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Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes von DU MONTCEL, Sophie Tezenas, DURR, Alexandra, VAN DE WARRENBURG, Bart P. C, ORSI, Laura, GIUNTI, Paola, FILLA, Alessandro, SZYMANSKI, Sandra, KLOCKGETHER, Thomas, BERCIANO, José, PANDOLFO, Massimo, BOESCH, Sylvia, MELEGH, Bela, BAUER, Peter, TIMMANN, Dagmar, MANDICH, Paola, CAMUZAT, Agnès, GOTO, Jun, ASHIZAWA, Tetsuo, CAZENEUVE, Cécile, TSUJI, Shoji, PULST, Stefan-M, BRUSCO, Alfredo, RIESS, Olaf, FIGUEROA, Karla P, BRICE, Alexis, STEVANIN, Giovanni, ICHIKAWA, Yaeko, BRUSSINO, Alessandro, FORLANI, Sylvie, RAKOWICZ, Maria, SCHÖLS, Ludger, MARIOTTI, Caterina

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Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects von Seong, Eunju, Insolera, Ryan, Dulovic, Marija, Kamsteeg, Erik‐Jan, Trinh, Joanne, Brüggemann, Norbert, Sandford, Erin, Li, Sheng, Ozel, Ayse Bilge, Li, Jun Z., Jewett, Tamison, Kievit, Anneke J. A., Münchau, Alexander, Shakkottai, Vikram, Klein, Christine, Collins, Catherine A., Lohmann, Katja, Warrenburg, Bart P., Burmeister, Margit

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Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease von Quadri, Marialuisa, Federico, Antonio, Zhao, Tianna, Breedveld, Guido J., Battisti, Carla, Delnooz, Cathérine, Severijnen, Lies-Anne, Di Toro Mammarella, Lara, Mignarri, Andrea, Monti, Lucia, Sanna, Antioco, Lu, Peng, Punzo, Francesca, Cossu, Giovanni, Willemsen, Rob, Rasi, Fabrizio, Oostra, Ben A., van de Warrenburg, Bart P., Bonifati, Vincenzo

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Therapeutic Misestimation in Patients with Degenerative Ataxia: Lessons from a Randomized Controlled Trial von Maas, Roderick P.P.W.M., Warrenburg, Bart P.C.

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Genotype, extrapyramidal features, and severity of variant ataxia‐telangiectasia von Schon, Katherine, van Os, Nienke J.H., Oscroft, Nicholas, Baxendale, Helen, Scoffings, Daniel, Ray, Julian, Suri, Mohnish, Whitehouse, William P., Mehta, Puja R., Everett, Natasha, Bottolo, Leonardo, Warrenburg, Bart P., Byrd, Philip J., Weemaes, Corry, Willemsen, Michel A., Tischkowitz, Marc, Taylor, A. Malcolm, Hensiek, Anke E.

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Cerebellar Transcranial Direct Current Stimulation in Spinocerebellar Ataxia Type 3: a Randomized, Double-Blind, Sham-Controlled Trial von Maas, Roderick P. P. W. M., Teerenstra, Steven, Toni, Ivan, Klockgether, Thomas, Schutter, Dennis J. L. G., van de Warrenburg, Bart P. C.

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Cerebellar Transcranial Direct Current Stimulation in the Cerebellar Cognitive Affective Syndrome: A Randomized, Double‐Blind, Sham‐Controlled Trial von Reumers, Stacha F.I., Maas, Roderick P.P.W.M., Schutter, Dennis J.L.G., Teerenstra, Steven, Kessels, Roy P.C., Leeuw, Frank‐Erik, Warrenburg, Bart P.C.

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A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder von Prooije, Teije H., Pennings, Maartje, Dorresteijn, Lucille, Gardeitchik, Thatjana, Odekerken, Vincent J.J., Oosterloo, Mayke, Pedersen, Annie, Verschuuren‐Bemelmans, Corien C., Vrancken, Alexander, Kamsteeg, Erik‐Jan, Warrenburg, Bart P.C.

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How to proceed after “negative” exome: A review on genetic diagnostics, limitations, challenges, and emerging new multiomics techniques von Wortmann, Saskia B., Oud, Machteld M., Alders, Mariëlle, Coene, Karlien L. M., Crabben, Saskia N., Feichtinger, René G., Garanto, Alejandro, Hoischen, Alex, Langeveld, Mirjam, Lefeber, Dirk, Mayr, Johannes A., Ockeloen, Charlotte W., Prokisch, Holger, Rodenburg, Richard, Waterham, Hans R., Wevers, Ron A., Warrenburg, Bart P. C., Willemsen, Michel A. A. P., Wolf, Nicole I., Vissers, Lisenka E. L. M., Karnebeek, Clara D. M.

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A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases von Neveling, Kornelia, Feenstra, Ilse, Gilissen, Christian, Hoefsloot, Lies H., Kamsteeg, Erik-Jan, Mensenkamp, Arjen R., Rodenburg, Richard J. T., Yntema, Helger G., Spruijt, Liesbeth, Vermeer, Sascha, Rinne, Tuula, van Gassen, Koen L., Bodmer, Danielle, Lugtenberg, Dorien, de Reuver, Rick, Buijsman, Wendy, Derks, Ronny C., Wieskamp, Nienke, van den Heuvel, Bert, Ligtenberg, Marjolijn J.L., Kremer, Hannie, Koolen, David A., van de Warrenburg, Bart P.C., Cremers, Frans P.M., Marcelis, Carlo L.M., Smeitink, Jan A.M., Wortmann, Saskia B., van Zelst-Stams, Wendy A.G., Veltman, Joris A., Brunner, Han G., Scheffer, Hans, Nelen, Marcel R.

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Responsiveness of the Scale for the Assessment and Rating of Ataxia and Natural History in 884 Recessive and Early Onset Ataxia Patients von Traschütz, Andreas, Adarmes‐Gómez, Astrid D., Anheim, Mathieu, Baets, Jonathan, Brais, Bernard, Gagnon, Cynthia, Gburek‐Augustat, Janina, Doss, Sarah, Hanağası, Haşmet A., Kamm, Christoph, Klivenyi, Peter, Klockgether, Thomas, Klopstock, Thomas, Minnerop, Martina, Münchau, Alexander, Renaud, Mathilde, Santorelli, Filippo M., Schöls, Ludger, Thieme, Andreas, Vielhaber, Stefan, Warrenburg, Bart P., Zanni, Ginevra, Hilgers, Ralf‐Dieter, Synofzik, Matthis

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Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3 von Maas, Roderick P.P.W.M., Teerenstra, Steven, Lima, Manuela, Pires, Paula, Pereira de Almeida, Luís, Gaalen, Judith, Timmann, Dagmar, Infante, Jon, Onyike, Chiadi, Bushara, Khalaf, Jacobi, Heike, Reetz, Kathrin, Santana, Magda M., Afonso Ribeiro, Joana, Hübener‐Schmid, Jeannette, Vries, Jeroen J., Synofzik, Matthis, Schöls, Ludger, Garcia‐Moreno, Hector, Giunti, Paola, Faber, Jennifer, Klockgether, Thomas, Warrenburg, Bart P.C.

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Task-free functional MRI in cervical dystonia reveals multi-network changes that partially normalize with botulinum toxin von Delnooz, Cathérine C S, Pasman, Jaco W, Beckmann, Christian F, van de Warrenburg, Bart P C

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Ataxia‐telangiectasia: recommendations for multidisciplinary treatment von Os, Nienke J H, Haaxma, Charlotte A, Flier, Michiel, Merkus, Peter J F M, Deuren, Marcel, Groot, Imelda J M, Loeffen, Jan, Warrenburg, Bart P C, Willemsen, Michèl A A P

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