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Results: 5

1.

DJ-1 Mutations are Rare in a Swedish Parkinson Cohort.

Anvret A, Blackinton JG, Westerlund M, Ran C, Sydow O, Willows T, HÃ¥kansson A, Nissbrandt H, Belin AC.

Open Neurol J. 2011 Mar 22;5:8-11. doi: 10.2174/1874205X01105010008.

PMID:
21532868
[PubMed]
Free PMC Article
2.

Absence of nigral degeneration in aged parkin/DJ-1/PINK1 triple knockout mice.

Kitada T, Tong Y, Gautier CA, Shen J.

J Neurochem. 2009 Nov;111(3):696-702. doi: 10.1111/j.1471-4159.2009.06350.x. Epub 2009 Aug 19.

PMID:
19694908
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2.

Bras J, Guerreiro R, Ribeiro M, Morgadinho A, Januario C, Dias M, Calado A, Semedo C, Oliveira C, Hardy J, Singleton A.

BMC Neurol. 2008 Jan 22;8:1. doi: 10.1186/1471-2377-8-1.

PMID:
18211709
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Merging mouse transcriptome analyses with Parkinson's disease linkage studies.

Gherbassi D, Bhatt L, Thuret S, Simon HH.

DNA Res. 2007 Apr;14(2):79-89. Epub 2007 May 23.

PMID:
17522092
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Neurodegenerative disorders: Parkinson's disease and Huntington's disease.

Hague SM, Klaffke S, Bandmann O.

J Neurol Neurosurg Psychiatry. 2005 Aug;76(8):1058-63. Review.

PMID:
16024878
[PubMed - indexed for MEDLINE]
Free PMC Article
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