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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 1 |
2010 | 5 |
2011 | 1 |
2024 | 0 |
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5 results
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Page 1
Calbindin-1 association and Parkinson's disease.
Eur J Neurol. 2010 Feb;17(2):208-11. doi: 10.1111/j.1468-1331.2009.02769.x. Epub 2009 Aug 5.
Eur J Neurol. 2010.
PMID: 19674066
Iron and reactive oxygen species activity in parkinsonian substantia nigra.
Wypijewska A, Galazka-Friedman J, Bauminger ER, Wszolek ZK, Schweitzer KJ, Dickson DW, Jaklewicz A, Elbaum D, Friedman A.
Wypijewska A, et al.
Parkinsonism Relat Disord. 2010 Jun;16(5):329-33. doi: 10.1016/j.parkreldis.2010.02.007. Epub 2010 Mar 9.
Parkinsonism Relat Disord. 2010.
PMID: 20219408
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SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction study.
Wider C, Vilariño-Güell C, Heckman MG, Jasinska-Myga B, Ortolaza-Soto AI, Diehl NN, Crook JE, Cobb SA, Bacon JA, Aasly JO, Gibson JM, Lynch T, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA.
Wider C, et al.
Eur J Neurol. 2011 Jun;18(6):876-81. doi: 10.1111/j.1468-1331.2010.03297.x. Epub 2010 Dec 15.
Eur J Neurol. 2011.
PMID: 21159074
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Mitochondrial translation initiation factor 3 polymorphism and Parkinson's disease.
Behrouz B, Vilariño-Güell C, Heckman MG, Soto-Ortolaza AI, Aasly JO, Sando S, Lynch T, Craig D, Uitti RJ, Wszolek ZK, Ross OA, Farrer MJ.
Behrouz B, et al.
Neurosci Lett. 2010 Dec 17;486(3):228-30. doi: 10.1016/j.neulet.2010.09.059. Epub 2010 Sep 29.
Neurosci Lett. 2010.
PMID: 20887776
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De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.
DeJesus-Hernandez M, Kocerha J, Finch N, Crook R, Baker M, Desaro P, Johnston A, Rutherford N, Wojtas A, Kennelly K, Wszolek ZK, Graff-Radford N, Boylan K, Rademakers R.
DeJesus-Hernandez M, et al.
Hum Mutat. 2010 May;31(5):E1377-89. doi: 10.1002/humu.21241.
Hum Mutat. 2010.
PMID: 20232451
Free PMC article.
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