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Current Treatment Options in Neurology|December 20, 2012
Limbic encephalitis and related cortical syndromesIgnacio Rubio-Agusti, Miguel Salavert, Luis BatallerRevista De Neurologia|April 14, 2010
[Familial idiopathic paroxysmal kinesigenic dyskinesia: its natural history and a descriptive study in three Spanish families]Juan Palau-Bargues, Ignacio Rubio-Agusti, Juan Andrés Burguera, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 20, 2013
Rest and other types of tremor in adult-onset primary dystoniaRoberto Erro, Ignacio Rubio-Agusti, Tabish A Saifee, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2012
Atypical parkinsonism and cerebrotendinous xanthomatosis: report of a family with corticobasal syndrome and a literature reviewIgnacio Rubio-Agusti, Maja Kojovic, Mark J Edwards, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 6, 2013
Functional (psychogenic) symptoms in Parkinson's diseaseIsabel Pareés, Tabish A Saifee, Maja Kojovic, et al.Brain : a Journal of Neurology|November 15, 2011
Believing is perceiving: mismatch between self-report and actigraphy in psychogenic tremorIsabel Pareés, Tabish A Saifee, Panagiotis Kassavetis, et al.Movement Disorders Clinical Practice|October 27, 2018
Expanding the Phenotype and Genetic Defects Associated with the GOSR2 GeneRoman Praschberger, Bettina Balint, Niccolo E Mencacci, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 11, 2015
Transcranial magnetic stimulation follow-up study in early Parkinson's disease: A decline in compensation with disease progression?Maja Kojovic, Panagiotis Kassavetis, Matteo Bologna, et al.Archives of Neurology|March 21, 2012
The brighter side of music in dystoniaMaja Kojovic, Isabel Pareés, Anna Sadnicka, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 21, 2014
The phenotypic spectrum of DYT24 due to ANO3 mutationsMaria Stamelou, Gavin Charlesworth, Carla Cordivari, et al.Pageof 2