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Page 1
Ethnic Differences in Dystonia Prevalence and Phenotype.
Mulroy E, Macerollo A, Scotton S, Cociasu I, Di Lazzaro G, Bashir S, Doherty J, Hamid S, Mooney N, Batla A, Morgante F, Bhatia KP. Mulroy E, et al. Among authors: morgante f. Mov Disord. 2022 Jun;37(6):1323-1325. doi: 10.1002/mds.29034. Epub 2022 May 2. Mov Disord. 2022. PMID: 35500158 No abstract available.
Abnormal sensorimotor plasticity in organic but not in psychogenic dystonia.
Quartarone A, Rizzo V, Terranova C, Morgante F, Schneider S, Ibrahim N, Girlanda P, Bhatia KP, Rothwell JC. Quartarone A, et al. Among authors: morgante f. Brain. 2009 Oct;132(Pt 10):2871-7. doi: 10.1093/brain/awp213. Epub 2009 Aug 18. Brain. 2009. PMID: 19690095 Free PMC article.
Lower limb involvement in adult-onset primary dystonia: frequency and clinical features.
Martino D, Macerollo A, Abbruzzese G, Bentivoglio AR, Berardelli A, Esposito M, Fabbrini G, Girlanda P, Guidubaldi A, Liguori R, Liuzzi D, Marinelli L, Morgante F, Sabetta A, Santoro L, Defazio G. Martino D, et al. Among authors: morgante f. Eur J Neurol. 2010 Feb;17(2):242-6. doi: 10.1111/j.1468-1331.2009.02781.x. Epub 2009 Sep 17. Eur J Neurol. 2010. PMID: 19765051
Environmental risk factors and clinical phenotype in familial and sporadic primary blepharospasm.
Defazio G, Abbruzzese G, Aniello MS, Bloise M, Crisci C, Eleopra R, Fabbrini G, Girlanda P, Liguori R, Macerollo A, Marinelli L, Martino D, Morgante F, Santoro L, Tinazzi M, Berardelli A. Defazio G, et al. Among authors: morgante f. Neurology. 2011 Aug 16;77(7):631-7. doi: 10.1212/WNL.0b013e3182299e13. Epub 2011 Jul 20. Neurology. 2011. PMID: 21775731
Eye symptoms in relatives of patients with primary adult-onset dystonia.
Defazio G, Abbruzzese G, Aniello MS, Di Fede R, Esposito M, Fabbrini G, Girlanda P, Liguori R, Marinelli L, Martino D, Morgante F, Santoro L, Tinazzi M, Berardelli A. Defazio G, et al. Among authors: morgante f. Mov Disord. 2012 Feb;27(2):305-7. doi: 10.1002/mds.24026. Epub 2011 Dec 15. Mov Disord. 2012. PMID: 22173654
Psychogenic facial movement disorders: clinical features and associated conditions.
Fasano A, Valadas A, Bhatia KP, Prashanth LK, Lang AE, Munhoz RP, Morgante F, Tarsy D, Duker AP, Girlanda P, Bentivoglio AR, Espay AJ. Fasano A, et al. Among authors: morgante f. Mov Disord. 2012 Oct;27(12):1544-51. doi: 10.1002/mds.25190. Epub 2012 Oct 2. Mov Disord. 2012. PMID: 23033125 Free PMC article.
Know thyself: Exploring interoceptive sensitivity in Parkinson's disease.
Ricciardi L, Ferrazzano G, Demartini B, Morgante F, Erro R, Ganos C, Bhatia KP, Berardelli A, Edwards M. Ricciardi L, et al. Among authors: morgante f. J Neurol Sci. 2016 May 15;364:110-5. doi: 10.1016/j.jns.2016.03.019. Epub 2016 Mar 12. J Neurol Sci. 2016. PMID: 27084227
Treatable inherited rare movement disorders.
Jinnah HA, Albanese A, Bhatia KP, Cardoso F, Da Prat G, de Koning TJ, Espay AJ, Fung V, Garcia-Ruiz PJ, Gershanik O, Jankovic J, Kaji R, Kotschet K, Marras C, Miyasaki JM, Morgante F, Munchau A, Pal PK, Rodriguez Oroz MC, Rodríguez-Violante M, Schöls L, Stamelou M, Tijssen M, Uribe Roca C, de la Cerda A, Gatto EM; International Parkinson's Disease Movement Disorders Society Task Force on Rare Movement Disorders. Jinnah HA, et al. Among authors: morgante f. Mov Disord. 2018 Jan;33(1):21-35. doi: 10.1002/mds.27140. Epub 2017 Sep 1. Mov Disord. 2018. PMID: 28861905 Free PMC article. Review.
206 results