EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood von van de Warrenburg, B. P. C., van Gaalen, J., Boesch, S., Burgunder, J.-M., Dürr, A., Giunti, P., Klockgether, T., Mariotti, C., Pandolfo, M., Riess, O.

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The Personalized Parkinson Project: examining disease progression through broad biomarkers in early Parkinson's disease von Bloem, B R, Marks, Jr, W J, Silva de Lima, A L, Kuijf, M L, van Laar, T, Jacobs, B P F, Verbeek, M M, Helmich, R C, van de Warrenburg, B P, Evers, L J W, intHout, J, van de Zande, T, Snyder, T M, Kapur, R, Meinders, M J

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The Use of the Voice Trainer App for Vocal Control in People with a Degenerative Ataxia: A Pilot Intervention Study von Knuijt, S., Nonnekes, J., van de Warrenburg, B. P. C., Nijkamp, M., Scholten, S., de Swart, B. J. M., Kalf, J. G.

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Inventory of Non-Ataxia Signs (INAS): Validation of a New Clinical Assessment Instrument von Jacobi, H., Rakowicz, M., Rola, R., Fancellu, R., Mariotti, C., Charles, P., Dürr, A., Küper, M., Timmann, D., Linnemann, C., Schöls, L., Kaut, O., Schaub, C., Filla, A., Baliko, L., Melegh, B., Kang, J.-S., Giunti, P., van de Warrenburg, B. P. C., Fimmers, R., Klockgether, T.

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Scale for the assessment and rating of ataxia : Development of a new clinical scale von SCHMITZ-HÜBSCH, T, TEZENAS DU MONTCEL, S, KREMER, B, MARIOTTI, C, MELEGH, B, PANDOLFO, M, RAKOWICZ, M, RIBAI, P, ROLA, R, SCHOLS, L, SZYMANSKI, S, VAN DE WARRENBURG, B. P, BALIKO, L, DÜRR, A, KLOCKGETHER, T, BERCIANO, J, BOESCH, S, DEPONDT, C, GIUNTI, P, GLOBAS, C, INFANTE, J, KANG, J.-S

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Botulinum toxin has an increased effect when targeted toward the muscle’s endplate zone: A high-density surface EMG guided study von Lapatki, B.G, van Dijk, J.P, van de Warrenburg, B.P.C, Zwarts, M.J

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Responsiveness of different rating instruments in spinocerebellar ataxia patients von SCHMITZ-HÜBSCH, T, FIMMERS, R, FILLA, A, SALVATORE, E, INFANTE, J, GIUNTI, P, LABRUM, R, KREMER, B, VAN DE WARRENBURG, B. P. C, BALIKO, L, MELEGH, B, DEPONDT, C, RAKOWICZ, M, SCHULZ, J, DU MONTCEL, S. Tezenas, KLOCKGETHER, T, ROLA, R, ZDZIENICKA, E, FANCELLU, R, MARIOTTI, C, LINNEMANN, C, SCHÖLS, L, TIMMANN, D

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SCA Functional Index : A useful compound performance measure for spinocerebellar ataxia von SCHMITZ-HÜBSCH, T, GIUNTI, P, VAN DE WARRENBURG, B. P. C, TIMMANN, D, FANCELLU, R, FROLA, R, DEPONDT, C, SCHÖLS, L, ZDZIENICKA, E, KANG, J.-S, DOHLINGER, S, KREMER, B, STEPHENSON, D. A, MELEGH, B, FILLA, A, KLOCKGETHER, T, GLOBAS, C, BALIKO, L, SACCA, F, MARIOTTI, C, RAKOWICZ, M, SZYMANSKI, S, INFANTE, J

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Cerebellum-dependent associative learning deficits in primary dystonia are normalized by rTMS and practice von Hoffland, B. S., Kassavetis, P., Bologna, M., Teo, J. T. H., Bhatia, K. P., Rothwell, J. C., Edwards, M. J., van de Warrenburg, B. P.

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Neurophysiological evidence for cerebellar dysfunction in primary focal dystonia von Teo, J T H, van de Warrenburg, B P C, Schneider, S A, Rothwell, J C, Bhatia, K P

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Spinocerebellar ataxia types 1, 2, 3, and 6 : Disease severity and nonataxia symptoms von SCHMITZ-HÜBSCH, T, COUDERT, M, RIBAI, P, SZYMANSKI, S, INFANTE, J, VAN DE WARRENBURG, B. P. C, DÜRR, A, TIMMANN, D, BOESCH, S, FANCELLU, R, ROLA, R, DEPONDT, C, BAUER, P, SCHÖLS, L, ZDIENICKA, E, KANG, J.-S, DÖHLINGER, S, KREMER, B, STEPHENSON, D. A, MELEGH, B, PANDOLFO, M, DI DONATO, S, TEZENAS DU MONTCEL, S, GIUNTI, P, KLOCKGETHER, T, GLOBAS, C, BALIKO, L, FILLA, A, MARIOTTI, C, RAKOWICZ, M, CHARLES, P

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Adult metachromatic leukodystrophy treated by allo-SCT and a review of the literature von de Hosson, L D, van de Warrenburg, B P C, Preijers, F W M B, Blijlevens, N M A, van der Reijden, B A, Kremer, H P H, Lefeber, D J, Allebes, W A, Al-Ali, H, Niederwieser, D W, Schaap, N P M, Schattenberg, A V M B

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Drug-Induced Cerebellar Ataxia: A Systematic Review von van Gaalen, J., Kerstens, F. G., Maas, R. P. P. W. M., Härmark, L., van de Warrenburg, B. P. C.

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Autosomal recessive cerebellar ataxias: the current state of affairs von Vermeer, S, van de Warrenburg, B P C, Willemsen, M A A P, Cluitmans, M, Scheffer, H, Kremer, B P, Knoers, N V A M

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Excessive short-latency stretch reflexes in the calf muscles do not cause postural instability in patients with hereditary spastic paraplegia von van Lith, B.J.H., de Niet, M., van de Warrenburg, B.P.C., Geurts, A.C., Weerdesteyn, V.

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Management of rare movement disorders in Europe: outcome of surveys of the European Reference Network for Rare Neurological Diseases von Painous, C., Os, N. J. H., Delamarre, A., Michailoviene, I., Marti, M. J., Warrenburg, B. P., Meissner, W. G., Utkus, A., Reinhard, C., Graessner, H., Tijssen, M. A.

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Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations von de Bot, S T, van den Elzen, R T M, Mensenkamp, A R, Schelhaas, H J, Willemsen, M A A P, Knoers, N V A M, Kremer, H P H, van de Warrenburg, B P C, Scheffer, H

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The natural history of spinocerebellar ataxia type 1, 2, 3, and 6 A 2-year follow-up study von JACOBI, H, BAUER, P, SCHÖLS, L, RAKOWICZ, M, ROLA, R, ZDZIENICKA, E, SCHMITZ-HUBSCH, T, FANCELLU, R, MARIOTTI, C, TOMASELLO, C, BALIKO, L, MELEGH, B, GIUNTI, P, FILLA, A, RINALDI, C, VAN DE WARRENBURG, B. P, VERSTAPPEN, C. C. P, SZYMANSKI, S, BERCIANO, J, INFANTE, J, TIMMANN, D, BOESCH, S, HERING, S, LABRUM, R, DEPONDT, C, PANDOLFO, M, KANG, J.-S, RATZKA, S, SCHULZ, J, TEZENAS DU MONTCEL, S, KLOCKGETHER, T, SWEENEY, M. G, CHARLES, P, DÜRR, A, MARELLI, C, GLOBAS, C, LINNEMANN, C

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Neurofilament light chain: A novel blood biomarker in patients with ataxia telangiectasia von Veenhuis, S.J.G., Gupta, A.S., de Gusmão, C.M., Thornton, J., Margus, B., Rothblum-Oviatt, C., Otto, M., Halbgebauer, S., van Os, N.J.H., van de Warrenburg, B.P.C., Verbeek, M.M., Willemsen, M.A.A.P.

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Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3 von Verbeek, D. S., van de Warrenburg, B. P., Wesseling, P., Pearson, P. L., Kremer, H. P., Sinke, R. J.

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