Showing results (1-10 of 11) with videos related to
Sort By:
Pageof 2
Movement Disorders : Official Journal of the Movement Disorder Society|February 22, 2024
Negative Myoclonus: Neurophysiological Study and Clinical Impact in Progressive Myoclonus AtaxiaLuca Pollini, Sterre van der Veen, Jan Willem J Elting, et al.International Journal of Molecular Sciences|August 23, 2020
KCND3-Related Neurological Disorders: From Old to Emerging Clinical PhenotypesLuca Pollini, Serena Galosi, Manuela Tolve, et al.Frontiers in Neurology|August 25, 2022
Motor, epileptic, and developmental phenotypes in genetic disorders affecting G protein coupled receptors-cAMP signalingSerena Galosi, Luca Pollini, Maria Novelli, et al.Neuropediatrics|July 2, 2025
Developmental and Epileptic Encephalopathy as a Novel Clinical Hallmark of SCA21Mario Mastrangelo, Giacomina Ricciardi, Carlo Greco, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|October 27, 2016
Attention in Parkinson's disease with fatigue: evidence from the attention network testCaterina Pauletti, Daniela Mannarelli, Nicoletta Locuratolo, et al.Molecular Genetics and Metabolism Reports|February 27, 2020
Multiple sclerosis and intracellular cobalamin defect (MMACHC/PRDX1) comorbidity in a young maleLuca Pollini, Manuela Tolve, Francesca Nardecchia, et al.Parkinsonism & Related Disorders|February 18, 2025
Eye movement disorders in genetic dystonia syndromes: A literature overviewLuca Pollini, Ilaria Pettenuzzo, Marina A J Tijssen, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|July 13, 2022
Neurophysiological assessment of juvenile parkinsonism due to primary monoamine neurotransmitter disordersMassimiliano Passaretti, Luca Pollini, Giulia Paparella, et al.Parkinsonism & Related Disorders|May 4, 2023
GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatmentsMaria Novelli, Serena Galosi, Giovanna Zorzi, et al.Cerebellum (London, England)|September 17, 2024
CACNA1G Causes Dominantly Inherited Myoclonus-Ataxia with Intellectual Disability: A Case ReportMartina De Riggi, Agnese De Giorgi, Luca Pollini, et al.Pageof 2