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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 5 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
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5 results
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Page 1
Genetic variability at the PARK16 locus.
Eur J Hum Genet. 2010 Dec;18(12):1356-9. doi: 10.1038/ejhg.2010.125. Epub 2010 Aug 4.
Eur J Hum Genet. 2010.
PMID: 20683486
Free PMC article.
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
UK Parkinson's Disease Consortium; Wellcome Trust Case Control Consortium 2; Spencer CC, Plagnol V, Strange A, Gardner M, Paisan-Ruiz C, Band G, Barker RA, Bellenguez C, Bhatia K, Blackburn H, Blackwell JM, Bramon E, Brown MA, Brown MA, Burn D, Casas JP, Chinnery PF, Clarke CE, Corvin A, Craddock N, Deloukas P, Edkins S, Evans J, Freeman C, Gray E, Hardy J, Hudson G, Hunt S, Jankowski J, Langford C, Lees AJ, Markus HS, Mathew CG, McCarthy MI, Morrison KE, Palmer CN, Pearson JP, Peltonen L, Pirinen M, Plomin R, Potter S, Rautanen A, Sawcer SJ, Su Z, Trembath RC, Viswanathan AC, Williams NW, Morris HR, Donnelly P, Wood NW.
UK Parkinson's Disease Consortium, et al.
Hum Mol Genet. 2011 Jan 15;20(2):345-53. doi: 10.1093/hmg/ddq469. Epub 2010 Nov 2.
Hum Mol Genet. 2011.
PMID: 21044948
Free PMC article.
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Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations.
Paisán-Ruiz C, Li A, Schneider SA, Holton JL, Johnson R, Kidd D, Chataway J, Bhatia KP, Lees AJ, Hardy J, Revesz T, Houlden H.
Paisán-Ruiz C, et al.
Neurobiol Aging. 2012 Apr;33(4):814-23. doi: 10.1016/j.neurobiolaging.2010.05.009. Epub 2010 Jul 21.
Neurobiol Aging. 2012.
PMID: 20619503
Free PMC article.
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Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
Paisán-Ruiz C, Guevara R, Federoff M, Hanagasi H, Sina F, Elahi E, Schneider SA, Schwingenschuh P, Bajaj N, Emre M, Singleton AB, Hardy J, Bhatia KP, Brandner S, Lees AJ, Houlden H.
Paisán-Ruiz C, et al.
Mov Disord. 2010 Sep 15;25(12):1791-800. doi: 10.1002/mds.23221.
Mov Disord. 2010.
PMID: 20669327
Free PMC article.
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Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA).
Kruer MC, Paisán-Ruiz C, Boddaert N, Yoon MY, Hama H, Gregory A, Malandrini A, Woltjer RL, Munnich A, Gobin S, Polster BJ, Palmeri S, Edvardson S, Hardy J, Houlden H, Hayflick SJ.
Kruer MC, et al.
Ann Neurol. 2010 Nov;68(5):611-8. doi: 10.1002/ana.22122.
Ann Neurol. 2010.
PMID: 20853438
Free PMC article.
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