doi: 10.1111/j.1532-5415.2007.01167.x.
Lrrking in the background: common pathways of neurodegeneration
- PMID: 17493210
- DOI: 10.1111/j.1532-5415.2007.01167.x
Item in Clipboard
Lrrking in the background: common pathways of neurodegeneration
J Am Geriatr Soc.
2007 May.
No abstract available
Similar articles
-
Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations.Neurology. 2008 Jul 22;71(4):303; author reply 303-4. doi: 10.1212/01.wnl.0000320511.30222.dd. Neurology. 2008. PMID: 18645174 No abstract available.
-
The importance of LRRK2 mutations in Parkinson disease.Arch Neurol. 2006 Sep;63(9):1225-8. doi: 10.1001/archneur.63.9.1225. Arch Neurol. 2006. PMID: 16966498 Review. No abstract available.
-
Up with the lark: a panoptic view of Parkinson disease.Neurology. 2011 Jul 26;77(4):310-1. doi: 10.1212/WNL.0b013e318227065d. Epub 2011 Jul 13. Neurology. 2011. PMID: 21753169 No abstract available.
-
Lrrk2 in the limelight!Neurology. 2007 Oct 30;69(18):1732-3. doi: 10.1212/01.wnl.0000279588.20391.88. Neurology. 2007. PMID: 17967990 No abstract available.
-
[Familial Parkinsonism].No To Shinkei. 2006 Aug;58(8):671-80. No To Shinkei. 2006. PMID: 16986673 Review. Japanese. No abstract available.
Cited by
-
Deletion of the WD40 domain of LRRK2 in Zebrafish causes Parkinsonism-like loss of neurons and locomotive defect.PLoS Genet. 2010 Apr 22;6(4):e1000914. doi: 10.1371/journal.pgen.1000914. PLoS Genet. 2010. PMID: 20421934 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
