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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 2 |
2009 | 3 |
2010 | 1 |
2024 | 0 |
Search Results
6 results
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Page 1
The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy.
Cell Death Differ. 2010 Jun;17(6):962-74. doi: 10.1038/cdd.2009.200. Epub 2010 Jan 8.
Cell Death Differ. 2010.
PMID: 20057503
Olfactory dysfunction in Parkinsonism caused by PINK1 mutations.
Ferraris A, Ialongo T, Passali GC, Pellecchia MT, Brusa L, Laruffa M, Guidubaldi A, Paludetti G, Albanese A, Barone P, Dallapiccola B, Valente EM, Bentivoglio AR.
Ferraris A, et al.
Mov Disord. 2009 Dec 15;24(16):2350-7. doi: 10.1002/mds.22816.
Mov Disord. 2009.
PMID: 19890973
Item in Clipboard
GIGYF2 variants are not associated with Parkinson's disease in Italy.
Bonetti M, Ferraris A, Petracca M, Bentivoglio AR, Dallapiccola B, Valente EM.
Bonetti M, et al.
Mov Disord. 2009 Sep 15;24(12):1867-8; author reply 1868-9. doi: 10.1002/mds.22640.
Mov Disord. 2009.
PMID: 19562763
No abstract available.
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Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson's disease by disturbing calcium flux.
Marongiu R, Spencer B, Crews L, Adame A, Patrick C, Trejo M, Dallapiccola B, Valente EM, Masliah E.
Marongiu R, et al.
J Neurochem. 2009 Mar;108(6):1561-74. doi: 10.1111/j.1471-4159.2009.05932.x. Epub 2009 Jan 24.
J Neurochem. 2009.
PMID: 19166511
Free PMC article.
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Genetic testing for paediatric neurological disorders.
Valente EM, Ferraris A, Dallapiccola B.
Valente EM, et al.
Lancet Neurol. 2008 Dec;7(12):1113-26. doi: 10.1016/S1474-4422(08)70257-6.
Lancet Neurol. 2008.
PMID: 19007736
Review.
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Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study.
Gelmetti V, Ferraris A, Brusa L, Romano F, Lombardi F, Barzaghi C, Stanzione P, Garavaglia B, Dallapiccola B, Valente EM.
Gelmetti V, et al.
Mov Disord. 2008 Apr 30;23(6):881-5. doi: 10.1002/mds.21960.
Mov Disord. 2008.
PMID: 18307263
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