未登录 分享 收藏
分享 收藏
分享 收藏
分享 收藏
分享 收藏
分享 收藏
分享 收藏
分享 收藏
A Screening Tool to Quickly Identify Movement Disorders in Patients with Inborn Errors of Metabolism Koens, Lisette H.; Klamer, Marrit R.; Sival, Deborah A.; Balint, Bettina; Bhatia, Kailash P.; Contarino, Maria Fiorella; van Egmond, Martje E.; Erro, Roberto; Friedman, Jennifer; Fung, Victor S. C.; Ganos, Christos; Kurian, Manju A.; Lang, Anthony E.; McGovern, Eavan M.; Roze, Emmanuel; de Koning, Tom J.; Tijssen, Marina A. J. 分享 收藏
Distinct movement disorders in contactin-associated-protein-like-2 antibody-associated autoimmune encephalitis contactin-associated-protein-like-2抗体相关自身免疫性脑炎的不同运动障碍 Goevert, Felix; Abrante, Ligia; Becktepe, Jos; Balint, Bettina; Ganos, Christos; Hofstadt-van Oy, Ulrich; Krogias, Christos; Varley, James; Irani, Sarosh R.; Paneva, Sofija; Titulaer, Maarten J.; de Vries, Juna M.; Boon, Agnita J. W.; Schreurs, Marco W. J.; Joubert, Bastien; Honnorat, Jerome; Vogrig, Alberto; Arino, Helena; Sabater, Lidia; Dalmau, Josep; Scotton, Sangeeta; Jacob, Saiju; Melzer, Nico; Bien, Christian G.; Geis, Christian; Lewerenz, Jan; Pruss, Harald; Wandinger, Klaus-Peter; Deuschl, Guenther; Leypoldt, Frank 分享 收藏
分享 收藏
分享 收藏
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism Magrinelli, Francesca; Mehta, Sahil; Di Lazzaro, Giulia; Latorre, Anna; Edwards, Mark J.; Balint, Bettina; Basu, Purba; Kobylecki, Christopher; Groppa, Sergiu; Hegde, Anaita; Mulroy, Eoin; Estevez-Fraga, Carlos; Arora, Anshita; Kumar, Hrishikesh; Schneider, Susanne A.; Lewis, Patrick A.; Jaunmuktane, Zane; Revesz, Tamas; Gandhi, Sonia; Wood, Nicholas W.; Hardy, John A.; Tinazzi, Michele; Lal, Vivek; Houlden, Henry; Bhatia, Kailash P. 分享 收藏
分享 收藏
Development of parkinsonism after long-standing cervical dystonia-A cohort Balint, Bettina; Mulroy, Eoin; Goevert, Felix; Latorre, Anna; Di Lazarro, Giulia; Erro, Roberto; Batla, Amit; Holton, Janice L.; Miki, Yasuo; Warner, Thomas T.; Bhatia, Kailash P. 分享 收藏
分享 收藏
分享 收藏
分享 收藏
Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia Mencacci, Niccolo E.; Brockmann, Marisa M.; Dai, Jinye; Pajusalu, Sander; Atasu, Burcu; Campos, Joaquin; Pino, Gabriela; Gonzalez-Latapi, Paulina; Patzke, Christopher; Schwake, Michael; Tucci, Arianna; Pittman, Alan; Simon-Sanchez, Javier; Carvill, Gemma L.; Balint, Bettina; Wiethoff, Sarah; Warner, Thomas T.; Papandreou, Apostolos; Soo, Audrey; Rein, Reet; Kadastik-Eerme, Liis; Puusepp, Sanna; Reinson, Karit; Tomberg, Tiiu; Hanagasi, Hasmet; Gasser, Thomas; Bhatia, Kailash P.; Kurian, Manju A.; Lohmann, Ebba; Ounap, Katrin; Rosenmund, Christian; Sudhof, Thomas C.; Wood, Nicholas W.; Krainc, Dimitri; Acuna, Claudio 分享 收藏
分享 收藏