KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia von Pennings, Maartje, Schouten, Meyke I., van Gaalen, Judith, Meijer, Rowdy P. P., de Bot, Susanne T., Kriek, Marjolein, Saris, Christiaan G. J., van den Berg, Leonard H., van Es, Michael A., Zuidgeest, Dick M. H., Elting, Mariet W., van de Kamp, Jiddeke M., van Spaendonck-Zwarts, Karin Y., Die-Smulders, Christine de, Brilstra, Eva H., Verschuuren, Corien C., de Vries, Bert B. A., Bruijn, Jacques, Sofou, Kalliopi, Duijkers, Floor A., Jaeger, B., Schieving, Jolanda H., van de Warrenburg, Bart P., Kamsteeg, Erik-Jan

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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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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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Therapeutic Strategies for Spinocerebellar Ataxia Type 1 von Kerkhof, Laurie M C, van de Warrenburg, Bart P C, van Roon-Mom, Willeke M C, Buijsen, Ronald A M

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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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Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene-disease associations and unanticipated rare disorders von van de Warrenburg, Bart P, Schouten, Meyke I, de Bot, Susanne T, Vermeer, Sascha, Meijer, Rowdy, Pennings, Maartje, Gilissen, Christian, Willemsen, Michèl Aap, Scheffer, Hans, Kamsteeg, Erik-Jan

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Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force von Marras, Connie, Lang, Anthony, van de Warrenburg, Bart P, Sue, Carolyn M, Tabrizi, Sarah J, Bertram, Lars, Mercimek-Mahmutoglu, Saadet, Ebrahimi-Fakhari, Darius, Warner, Thomas T, Durr, Alexandra, Assmann, Birgit, Lohmann, Katja, Kostic, Vladimir, Klein, Christine

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ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia von Vermeer, Sascha, Meijer, Rowdy P. P., Pijl, Benjamin J., Timmermans, Janneke, Cruysberg, Johannes R. M., Bos, Maaike M., Schelhaas, Helenius J., van de Warrenburg, Bart. P. C., Knoers, Nine V. A. M., Scheffer, Hans, Kremer, Berry

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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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Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias von Jacobi, Heike, du Montcel, Sophie Tezenas, Bauer, Peter, Giunti, Paola, Cook, Arron, Labrum, Robyn, Parkinson, Michael H., Durr, Alexandra, Brice, Alexis, Charles, Perrine, Marelli, Cecilia, Mariotti, Caterina, Nanetti, Lorenzo, Sarro, Lidia, Rakowicz, Maria, Sulek, Anna, Sobanska, Anna, Schmitz-Hübsch, Tanja, Schöls, Ludger, Hengel, Holger, Baliko, Laszlo, Melegh, Bela, Filla, Alessandro, Antenora, Antonella, Infante, Jon, Berciano, José, van de Warrenburg, Bart P., Timmann, Dagmar, Szymanski, Sandra, Boesch, Sylvia, Nachbauer, Wolfgang, Kang, Jun-Suk, Pandolfo, Massimo, Schulz, Jörg B., Melac, Audrey Tanguy, Diallo, Alhassane, Klockgether, Thomas

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Abnormal eyeblink conditioning is an early marker of cerebellar dysfunction in preclinical SCA3 mutation carriers von van Gaalen, J., Maas, R. P. P. W. M., Ippel, E. F., Elting, M. W., van Spaendonck-Zwarts, K. Y., Vermeer, S., Verschuuren-Bemelmans, C., Timmann, D., van de Warrenburg, Bart P.

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Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19 von Duarri, Anna, Jezierska, Justyna, Fokkens, Michiel, Meijer, Michel, Schelhaas, Helenius J., den Dunnen, Wilfred F. A., van Dijk, Freerk, Verschuuren-Bemelmans, Corien, Hageman, Gerard, van de Vlies, Pieter, Küsters, Benno, van de Warrenburg, Bart P., Kremer, Berry, Wijmenga, Cisca, Sinke, Richard J., Swertz, Morris A., Kampinga, Harm H., Boddeke, Erik, Verbeek, Dineke S.

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Experienced complaints, activity limitations and loss of motor capacities in patients with pure hereditary spastic paraplegia: a web-based survey in the Netherlands von van Lith, Bas J H, Kerstens, Hans C J W, van den Bemd, Laura A C, der Sanden, Maria W G Nijhuis-van, Weerdesteyn, Vivian, Smeets, Rob J E M, Fheodoroff, Klemens, van de Warrenburg, Bart P C, Geurts, Alexander C H

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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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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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Altered striatal and pallidal connectivity in cervical dystonia von Delnooz, Cathérine C. S., Pasman, Jaco W., Beckmann, Christian F., van de Warrenburg, Bart P. C.

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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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Cerebellar transcranial direct current stimulation in spinocerebellar ataxia type 3 (SCA3-tDCS): rationale and protocol of a randomized, double-blind, sham-controlled study von Maas, Roderick P P W M, Toni, Ivan, Doorduin, Jonne, Klockgether, Thomas, Schutter, Dennis J L G, van de Warrenburg, Bart P C

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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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Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia von Vermeer, Sascha, Hoischen, Alexander, Meijer, Rowdy P.P., Gilissen, Christian, Neveling, Kornelia, Wieskamp, Nienke, de Brouwer, Arjan, Koenig, Michel, Anheim, Mathieu, Assoum, Mirna, Drouot, Nathalie, Todorovic, Slobodanka, Milic-Rasic, Vedrana, Lochmüller, Hanns, Stevanin, Giovanni, Goizet, Cyril, David, Albert, Durr, Alexandra, Brice, Alexis, Kremer, Berry, van de Warrenburg, Bart P.C., Schijvenaars, Mascha M.V.A.P., Heister, Angelien, Kwint, Michael, Arts, Peer, van der Wijst, Jenny, Veltman, Joris, Kamsteeg, Erik-Jan, Scheffer, Hans, Knoers, Nine

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