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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 1 |
2009 | 1 |
2012 | 2 |
2017 | 1 |
2018 | 1 |
2024 | 0 |
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4 results
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Page 1
Rapid genetic diagnosis in single-gene movement disorders.
Mov Disord. 2012 Apr;27(4):467-9. doi: 10.1002/mds.24896.
Mov Disord. 2012.
PMID: 22488858
Free PMC article.
No abstract available.
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal.
Bras J, Paisan-Ruiz C, Guerreiro R, Ribeiro MH, Morgadinho A, Januario C, Sidransky E, Oliveira C, Singleton A.
Bras J, et al.
Neurobiol Aging. 2009 Sep;30(9):1515-7. doi: 10.1016/j.neurobiolaging.2007.11.016. Epub 2007 Dec 21.
Neurobiol Aging. 2009.
PMID: 18160183
Free PMC article.
Item in Clipboard
Lewy-like aggregation of α-synuclein reduces protein phosphatase 2A activity in vitro and in vivo.
Wu J, Lou H, Alerte TN, Stachowski EK, Chen J, Singleton AB, Hamilton RL, Perez RG.
Wu J, et al.
Neuroscience. 2012 Apr 5;207:288-97. doi: 10.1016/j.neuroscience.2012.01.028. Epub 2012 Jan 25.
Neuroscience. 2012.
PMID: 22326202
Free PMC article.
Item in Clipboard
Leucine rich repeat kinase knockout (LRRK KO) mouse model: Linking pathological hallmarks of inherited and sporadic Parkinson's disease.
Roosen DA, Singleton AB.
Roosen DA, et al.
Mov Disord. 2018 Jan;33(1):72. doi: 10.1002/mds.27267. Epub 2017 Dec 19.
Mov Disord. 2018.
PMID: 29265552
Free PMC article.
No abstract available.
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