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Journal Article
Delle Vedove, A., Zanni, G., Eckenweiler, M., Storbeck, M., Barresi, S., Pizzi, S., Hosseinibarkooie, S., Mendoza-Ferreira, N., Hoelker, I., Koerber, F., Kye, M., Bertini, E., Kirschner, J., Tartaglia, M. and Wirth, B. (2020). A recurrent de novo CAPRIN1 mutation causes a novel progressive early onset neurodegenerative disorder. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 404 - 405. LONDON: SPRINGERNATURE. ISSN 1476-5438
Koy, A., Bockhorn, N., Kuehn, A. A., Schneider, G-H, Krause, P., Lauritsch, K., Witt, K., Paschen, S., Deuschl, G., Krauss, J. K., Saryyeva, A., Runge, J., Borggraefe, I, Mehrkens, J. H., Horn, A., Vesper, J., Schnitzler, A., Siegert, S., Freilinger, M., Eckenweiler, M., Coenen, V. A., Tadic, V, Voges, J., Pauls, K. A. M., Wirths, J., Timmermann, L. and Hellmich, M. (2019). Adverse events associated with deep brain stimulation in patients with childhood-onset dystonia. Brain Stimul., 12 (5). S. 1111 - 1121. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1876-4754