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

Year Number of Results
2008 3
2011 2
2012 9
2013 5
2014 8
2015 1
2016 4
2017 2
2022 0
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28 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, Press R, Lunn MP, Lim M, Maddison P, Meinck HM, Vandenberghe W, Vincent A. Carvajal-González A, et al. Among authors: sheerin um. Brain. 2014 Aug;137(Pt 8):2178-92. doi: 10.1093/brain/awu142. Epub 2014 Jun 20. Brain. 2014. PMID: 24951641 Free PMC article.
Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation.
Abbas MM, Govindappa ST, Sheerin UM, Bhatia KP, Muthane UB. Abbas MM, et al. Among authors: sheerin um. Mov Disord Clin Pract. 2016 Apr 26;4(1):132-135. doi: 10.1002/mdc3.12353. eCollection 2017 Jan-Feb. Mov Disord Clin Pract. 2016. PMID: 30713959 Free PMC article. No abstract available.
Screening for VPS35 mutations in Parkinson's disease.
Sheerin UM, Charlesworth G, Bras J, Guerreiro R, Bhatia K, Foltynie T, Limousin P, Silveira-Moriyama L, Lees A, Wood N. Sheerin UM, et al. Neurobiol Aging. 2012 Apr;33(4):838.e1-5. doi: 10.1016/j.neurobiolaging.2011.10.032. Epub 2011 Dec 7. Neurobiol Aging. 2012. PMID: 22154191 Free PMC article.
The entity of parkinsonism and associated lipomatosis.
Stamelou M, Sheerin UM, Wood N, Bhatia KP. Stamelou M, et al. Among authors: sheerin um. 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.
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. Among authors: sheerin um. 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. Among authors: sheerin um. 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.
28 results