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Movement Disorders : Official Journal of the Movement Disorder Society|October 29, 2014
Patients with scans without evidence of dopaminergic deficit: a long-term follow-up studyAmit Batla, Roberto Erro, Maria Stamelou, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 10, 2013
Familial psychogenic movement disordersMaria Stamelou, Giovanni Cossu, Mark J Edwards, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 19, 2013
Functional movement disorders are not uncommon in the elderlyAmit Batla, Maria Stamelou, Mark J Edwards, et al.Parkinsonism & Related Disorders|June 11, 2013
Markedly asymmetric presentation in multiple system atrophyAmit Batla, Maria Stamelou, Katerina Mensikova, et al.Parkinsonism & Related Disorders|August 21, 2020
Isolated and combined genetic tremor syndromes: a critical appraisal based on the 2018 MDS criteriaFrancesca Magrinelli, Anna Latorre, Bettina Balint, et al.Parkinsonism & Related Disorders|June 5, 2014
Facial tremor in dystoniaRoberto Erro, Maria Stamelou, Tabish A Saifee, et al.Parkinsonism & Related Disorders|October 5, 2013
Psychogenic paroxysmal movement disorders--clinical features and diagnostic cluesChristos Ganos, Maria Aguirregomozcorta, Amit Batla, et al.Neurology|July 21, 2012
Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiencyMaria Stamelou, Niccolo E Mencacci, Carla Cordivari, et al.Journal of Neurology|December 1, 2012
Patients with rest-tremor and scans with ipsilateral dopaminergic deficitMaria Aguirregomozcorta, Maria Stamelou, Angelo Antonini, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 29, 2012
Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorderMaria Stamelou, Karin Tuschl, W K Chong, et al.Pageof 53