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Year Number of Results
2009 1
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2011 4
2012 6
2013 7
2014 4
2015 3
2024 0

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24 results

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Page 1
Limbic encephalitis and related cortical syndromes.
Rubio-Agusti I, Salavert M, Bataller L. Rubio-Agusti I, et al. Curr Treat Options Neurol. 2013 Apr;15(2):169-84. doi: 10.1007/s11940-012-0212-7. Curr Treat Options Neurol. 2013. PMID: 23250843
Functional (psychogenic) symptoms in Parkinson's disease.
Pareés I, Saifee TA, Kojovic M, Kassavetis P, Rubio-Agusti I, Sadnicka A, Bhatia KP, Edwards MJ. Pareés I, et al. Among authors: rubio agusti i. Mov Disord. 2013 Oct;28(12):1622-7. doi: 10.1002/mds.25544. Epub 2013 Jun 4. Mov Disord. 2013. PMID: 23737007
Physical precipitating factors in functional movement disorders.
Pareés I, Kojovic M, Pires C, Rubio-Agusti I, Saifee TA, Sadnicka A, Kassavetis P, Macerollo A, Bhatia KP, Carson A, Stone J, Edwards MJ. Pareés I, et al. Among authors: rubio agusti i. J Neurol Sci. 2014 Mar 15;338(1-2):174-7. doi: 10.1016/j.jns.2013.12.046. Epub 2014 Jan 8. J Neurol Sci. 2014. PMID: 24439198
The syndrome of deafness-dystonia: clinical and genetic heterogeneity.
Kojovic M, Pareés I, Lampreia T, Pienczk-Reclawowicz K, Xiromerisiou G, Rubio-Agusti I, Kramberger M, Carecchio M, Alazami AM, Brancati F, Slawek J, Pirtosek Z, Valente EM, Alkuraya FS, Edwards MJ, Bhatia KP. Kojovic M, et al. Among authors: rubio agusti i. Mov Disord. 2013 Jun;28(6):795-803. doi: 10.1002/mds.25394. Epub 2013 Feb 15. Mov Disord. 2013. PMID: 23418071
The brighter side of music in dystonia.
Kojovic M, Pareés I, Sadnicka A, Kassavetis P, Rubio-Agusti I, Saifee TA, Bologna M, Rothwell JC, Edwards MJ, Bhatia KP. Kojovic M, et al. Among authors: rubio agusti i. Arch Neurol. 2012 Jul;69(7):917-9. doi: 10.1001/archneurol.2012.33. Arch Neurol. 2012. PMID: 22431838
Movement disorders in adult patients with classical galactosemia.
Rubio-Agusti I, Carecchio M, Bhatia KP, Kojovic M, Parees I, Chandrashekar HS, Footitt EJ, Burke D, Edwards MJ, Lachmann RH, Murphy E. Rubio-Agusti I, et al. Mov Disord. 2013 Jun;28(6):804-10. doi: 10.1002/mds.25348. Epub 2013 Feb 11. Mov Disord. 2013. PMID: 23400815
Isolated hemidystonia associated with NMDA receptor antibodies.
Rubio-Agustí I, Dalmau J, Sevilla T, Burgal M, Beltrán E, Bataller L. Rubio-Agustí I, et al. Mov Disord. 2011 Feb 1;26(2):351-2. doi: 10.1002/mds.23315. Epub 2010 Dec 15. Mov Disord. 2011. PMID: 21412839 Free PMC article. No abstract available.
The phenotypic spectrum of DYT24 due to ANO3 mutations.
Stamelou M, Charlesworth G, Cordivari C, Schneider SA, Kägi G, Sheerin UM, Rubio-Agusti I, Batla A, Houlden H, Wood NW, Bhatia KP. Stamelou M, et al. Among authors: rubio agusti i. Mov Disord. 2014 Jun;29(7):928-34. doi: 10.1002/mds.25802. Epub 2014 Jan 17. Mov Disord. 2014. PMID: 24442708 Free PMC article.
Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene.
Praschberger R, Balint B, Mencacci NE, Hersheson J, Rubio-Agusti I, Kullmann DM, Bettencourt C, Bhatia K, Houlden H. Praschberger R, et al. Among authors: rubio agusti i. Mov Disord Clin Pract. 2015 Jun 17;2(3):271-273. doi: 10.1002/mdc3.12190. eCollection 2015 Sep. Mov Disord Clin Pract. 2015. PMID: 30363482 Free PMC article.
24 results