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

Year Number of Results
2011 2
2012 10
2013 8
2014 8
2020 0
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23 results
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Page 1
Glycine receptor antibodies in PERM and related syndromes: characteristics, clinical features and outcomes.
Carvajal-González A, Leite MI, Waters P, Woodhall M, Coutinho E, Balint B, Lang B, Pettingill P, Carr A, Sheerin UM, Press R, Lunn MP, Lim M, Maddison P, Meinck HM, Vandenberghe W, Vincent A. Carvajal-González A, et al. Brain. 2014 Aug;137(Pt 8):2178-92. doi: 10.1093/brain/awu142. Epub 2014 Jun 20. Brain. 2014. PMID: 24951641 Free PMC article.
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
International Parkinson Disease Genomics Consortium, Nalls MA, Plagnol V, Hernandez DG, Sharma M, Sheerin UM, Saad M, Simón-Sánchez J, Schulte C, Lesage S, Sveinbjörnsdóttir S, Stefánsson K, Martinez M, Hardy J, Heutink P, Brice A, Gasser T, Singleton AB, Wood NW. International Parkinson Disease Genomics Consortium, et al. Lancet. 2011 Feb 19;377(9766):641-9. doi: 10.1016/S0140-6736(10)62345-8. Epub 2011 Feb 1. Lancet. 2011. PMID: 21292315 Free PMC article.
Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.
Erro R, Sheerin UM, Bhatia KP. Erro R, et al. Mov Disord. 2014 Aug;29(9):1108-16. doi: 10.1002/mds.25933. Epub 2014 Jun 25. Mov Disord. 2014. PMID: 24963779 Review.
Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.
Wray S, Self M; NINDS Parkinson's Disease iPSC Consortium; NINDS Huntington's Disease iPSC Consortium; NINDS ALS iPSC Consortium, Lewis PA, Taanman JW, Ryan NS, Mahoney CJ, Liang Y, Devine MJ, Sheerin UM, Houlden H, Morris HR, Healy D, Marti-Masso JF, Preza E, Barker S, Sutherland M, Corriveau RA, D'Andrea M, Schapira AH, Uitti RJ, Guttman M, Opala G, Jasinska-Myga B, Puschmann A, Nilsson C, Espay AJ, Slawek J, Gutmann L, Boeve BF, Boylan K, Stoessl AJ, Ross OA, Maragakis NJ, Van Gerpen J, Gerstenhaber M, Gwinn K, Dawson TM, Isacson O, Marder KS, Clark LN, Przedborski SE, Finkbeiner S, Rothstein JD, Wszolek ZK, Rossor MN, Hardy J. Wray S, et al. PLoS One. 2012;7(8):e43099. doi: 10.1371/journal.pone.0043099. Epub 2012 Aug 27. PLoS One. 2012. PMID: 22952635 Free PMC article.
The entity of parkinsonism and associated lipomatosis.
Stamelou M, Sheerin UM, Wood N, Bhatia KP. Stamelou M, et al. Neurology. 2014 Oct 28;83(18):1673-4. doi: 10.1212/WNL.0000000000000937. Epub 2014 Oct 1. Neurology. 2014. PMID: 25274843 Free PMC article. No abstract available.
ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystonia.
Sheerin UM, Schneider SA, Carr L, Deuschl G, Hopfner F, Stamelou M, Wood NW, Bhatia KP. Sheerin UM, et al. Neurology. 2014 Mar 25;82(12):1065-7. doi: 10.1212/WNL.0000000000000254. Epub 2014 Feb 21. Neurology. 2014. PMID: 24562058 Free PMC article.
Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration.
Tsika E, Glauser L, Moser R, Fiser A, Daniel G, Sheerin UM, Lees A, Troncoso JC, Lewis PA, Bandopadhyay R, Schneider BL, Moore DJ. Tsika E, et al. Hum Mol Genet. 2014 Sep 1;23(17):4621-38. doi: 10.1093/hmg/ddu178. Epub 2014 Apr 15. Hum Mol Genet. 2014. PMID: 24740878 Free PMC article.
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.
Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation.
Sheerin UM, Stamelou M, Charlesworth G, Shiner T, Spacey S, Valente EM, Wood NW, Bhatia KP. Sheerin UM, et al. J Neurol. 2013 Feb;260(2):656-60. doi: 10.1007/s00415-012-6747-4. Epub 2012 Nov 24. J Neurol. 2013. PMID: 23180180 Free PMC article. No abstract available.
Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations.
Proukakis C, Shoaee M, Morris J, Brier T, Kara E, Sheerin UM, Charlesworth G, Tolosa E, Houlden H, Wood NW, Schapira AH. Proukakis C, et al. Mov Disord. 2014 Jul;29(8):1060-4. doi: 10.1002/mds.25883. Epub 2014 Apr 21. Mov Disord. 2014. PMID: 24752924 Free PMC article.
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