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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1998 1
1999 1
2001 1
2002 6
2003 4
2004 3
2005 3
2006 3
2007 1
2009 3
2010 3
2011 7
2012 9
2013 15
2014 24
2015 19
2016 17
2017 21
2018 17
2019 16
2020 17
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Similar Articles for PMID: 25643588

174 results
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Page 1
Dystonia: an update on phenomenology, classification, pathogenesis and treatment.
Balint B, Bhatia KP. Balint B, et al. Curr Opin Neurol. 2014 Aug;27(4):468-76. doi: 10.1097/WCO.0000000000000114. Curr Opin Neurol. 2014. PMID: 24978640 Review.
The monogenic primary dystonias.
Müller U. Müller U. Brain. 2009 Aug;132(Pt 8):2005-25. doi: 10.1093/brain/awp172. Epub 2009 Jul 3. Brain. 2009. PMID: 19578124 Review.
Dystonia.
Morgante F, Klein C. Morgante F, et al. Continuum (Minneap Minn). 2013 Oct;19(5 Movement Disorders):1225-41. doi: 10.1212/01.CON.0000436154.08791.67. Continuum (Minneap Minn). 2013. PMID: 24092288 Review.
The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.
Sweney MT, Newcomb TM, Swoboda KJ. Sweney MT, et al. Pediatr Neurol. 2015 Jan;52(1):56-64. doi: 10.1016/j.pediatrneurol.2014.09.015. Epub 2014 Oct 13. Pediatr Neurol. 2015. PMID: 25447930 Free PMC article. Review.
Update on the Genetics of Dystonia.
Lohmann K, Klein C. Lohmann K, et al. Curr Neurol Neurosci Rep. 2017 Mar;17(3):26. doi: 10.1007/s11910-017-0735-0. Curr Neurol Neurosci Rep. 2017. PMID: 28283962 Review.
Chapter 33: the history of movement disorders.
Lanska DJ. Lanska DJ. Handb Clin Neurol. 2010;95:501-46. doi: 10.1016/S0072-9752(08)02133-7. Handb Clin Neurol. 2010. PMID: 19892136 Review.
Genetics in dystonia.
Klein C. Klein C. Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S137-42. doi: 10.1016/S1353-8020(13)70033-6. Parkinsonism Relat Disord. 2014. PMID: 24262166 Review.
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.
Clot F, Grabli D, Cazeneuve C, Roze E, Castelnau P, Chabrol B, Landrieu P, Nguyen K, Ponsot G, Abada M, Doummar D, Damier P, Gil R, Thobois S, Ward AJ, Hutchinson M, Toutain A, Picard F, Camuzat A, Fedirko E, Sân C, Bouteiller D, LeGuern E, Durr A, Vidailhet M, Brice A; French Dystonia Network. Clot F, et al. Brain. 2009 Jul;132(Pt 7):1753-63. doi: 10.1093/brain/awp084. Epub 2009 Jun 2. Brain. 2009. PMID: 19491146
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. 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.
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