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

Year Number of Results
2008 3
2009 4
2010 4
2011 4
2012 2
2013 3
2014 11
2015 7
2016 6
2017 7
2018 4
2019 5
2020 3
2021 2
2022 2
2024 0

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54 results

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Page 1
DNAJC12 and dopa-responsive nonprogressive parkinsonism.
Straniero L, Guella I, Cilia R, Parkkinen L, Rimoldi V, Young A, Asselta R, Soldà G, Sossi V, Stoessl AJ, Priori A, Nishioka K, Hattori N, Follett J, Rajput A, Blau N, Pezzoli G, Farrer MJ, Goldwurm S, Rajput AH, Duga S. Straniero L, et al. Among authors: guella i. Ann Neurol. 2017 Oct;82(4):640-646. doi: 10.1002/ana.25048. Epub 2017 Oct 11. Ann Neurol. 2017. PMID: 28892570
Functional impairment of cortical AMPA receptors in schizophrenia.
Zeppillo T, Schulmann A, Macciardi F, Hjelm BE, Föcking M, Sequeira PA, Guella I, Cotter D, Bunney WE, Limon A, Vawter MP. Zeppillo T, et al. Among authors: guella i. Schizophr Res. 2022 Nov;249:25-37. doi: 10.1016/j.schres.2020.03.037. Epub 2020 Jun 6. Schizophr Res. 2022. PMID: 32513544 Free PMC article.
Novel LRRK2 mutations in Parkinsonism.
Trinh J, Guella I, McKenzie M, Gustavsson EK, Szu-Tu C, Petersen MS, Rajput A, Rajput AH, McKeown M, Jeon BS, Aasly JO, Bardien S, Farrer MJ. Trinh J, et al. Among authors: guella i. Parkinsonism Relat Disord. 2015 Sep;21(9):1119-21. doi: 10.1016/j.parkreldis.2015.07.011. Epub 2015 Jul 18. Parkinsonism Relat Disord. 2015. PMID: 26213354 No abstract available.
DNAJC13 genetic variants in parkinsonism.
Gustavsson EK, Trinh J, Guella I, Vilariño-Güell C, Appel-Cresswell S, Stoessl AJ, Tsui JK, McKeown M, Rajput A, Rajput AH, Aasly JO, Farrer MJ. Gustavsson EK, et al. Among authors: guella i. Mov Disord. 2015 Feb;30(2):273-8. doi: 10.1002/mds.26064. Epub 2014 Nov 12. Mov Disord. 2015. PMID: 25393719
Glucocerebrosidase mutations in primary parkinsonism.
Asselta R, Rimoldi V, Siri C, Cilia R, Guella I, Tesei S, Soldà G, Pezzoli G, Duga S, Goldwurm S. Asselta R, et al. Among authors: guella i. Parkinsonism Relat Disord. 2014 Nov;20(11):1215-20. doi: 10.1016/j.parkreldis.2014.09.003. Epub 2014 Sep 9. Parkinsonism Relat Disord. 2014. PMID: 25249066 Free PMC article.
DCTN1 p.K56R in progressive supranuclear palsy.
Gustavsson EK, Trinh J, Guella I, Szu-Tu C, Khinda J, Lin CH, Wu RM, Stoessl J, Appel-Cresswell S, McKeown M, Rajput A, Rajput AH, Petersen MS, Jeon BS, Aasly JO, Farrer MJ. Gustavsson EK, et al. Among authors: guella i. Parkinsonism Relat Disord. 2016 Jul;28:56-61. doi: 10.1016/j.parkreldis.2016.04.025. Epub 2016 Apr 23. Parkinsonism Relat Disord. 2016. PMID: 27132499
Parkinsonism in GTP cyclohydrolase 1 mutation carriers.
Guella I, Sherman HE, Appel-Cresswell S, Rajput A, Rajput AH, Farrer MJ. Guella I, et al. Brain. 2015 May;138(Pt 5):e349. doi: 10.1093/brain/awu341. Epub 2014 Dec 13. Brain. 2015. PMID: 25497597 Free PMC article. No abstract available.
A Meta-Analysis of α-Synuclein Multiplication in Familial Parkinsonism.
Book A, Guella I, Candido T, Brice A, Hattori N, Jeon B, Farrer MJ; SNCA Multiplication Investigators of the GEoPD Consortium. Book A, et al. Among authors: guella i. Front Neurol. 2018 Dec 11;9:1021. doi: 10.3389/fneur.2018.01021. eCollection 2018. Front Neurol. 2018. PMID: 30619023 Free PMC article.
Hunting for Familial Parkinson's Disease Mutations in the Post Genome Era.
Bentley SR, Guella I, Sherman HE, Neuendorf HM, Sykes AM, Fowdar JY, Silburn PA, Wood SA, Farrer MJ, Mellick GD. Bentley SR, et al. Among authors: guella i. Genes (Basel). 2021 Mar 17;12(3):430. doi: 10.3390/genes12030430. Genes (Basel). 2021. PMID: 33802862 Free PMC article.
Dopamine receptors and BDNF-haplotypes predict dyskinesia in Parkinson's disease.
Kusters CDJ, Paul KC, Guella I, Bronstein JM, Sinsheimer JS, Farrer MJ, Ritz BR. Kusters CDJ, et al. Among authors: guella i. Parkinsonism Relat Disord. 2018 Feb;47:39-44. doi: 10.1016/j.parkreldis.2017.11.339. Epub 2017 Nov 24. Parkinsonism Relat Disord. 2018. PMID: 29191473 Free PMC article.
54 results