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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 1
1990 2
1991 1
1992 1
1994 2
1995 2
1996 1
1997 3
1998 3
1999 1
2000 1
2001 1
2002 2
2003 1
2004 3
2005 2
2006 4
2008 6
2018 1
2024 0

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PubMed (OMIM) for id: 6620

38 results

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Page 1
A novel PSEN2 mutation associated with a peculiar phenotype.
Piscopo P, Marcon G, Piras MR, Crestini A, Campeggi LM, Deiana E, Cherchi R, Tanda F, Deplano A, Vanacore N, Tagliavini F, Pocchiari M, Giaccone G, Confaloni A. Piscopo P, et al. Neurology. 2008 Apr 22;70(17):1549-54. doi: 10.1212/01.wnl.0000310643.53587.87. Neurology. 2008. PMID: 18427071
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.
Mata IF, Samii A, Schneer SH, Roberts JW, Griffith A, Leis BC, Schellenberg GD, Sidransky E, Bird TD, Leverenz JB, Tsuang D, Zabetian CP. Mata IF, et al. Arch Neurol. 2008 Mar;65(3):379-82. doi: 10.1001/archneurol.2007.68. Arch Neurol. 2008. PMID: 18332251 Free PMC article.
Biochemical and pathological characterization of Lrrk2.
Giasson BI, Covy JP, Bonini NM, Hurtig HI, Farrer MJ, Trojanowski JQ, Van Deerlin VM. Giasson BI, et al. Ann Neurol. 2006 Feb;59(2):315-22. doi: 10.1002/ana.20791. Ann Neurol. 2006. PMID: 16437584
Lrrk2 and Lewy body disease.
Ross OA, Toft M, Whittle AJ, Johnson JL, Papapetropoulos S, Mash DC, Litvan I, Gordon MF, Wszolek ZK, Farrer MJ, Dickson DW. Ross OA, et al. Ann Neurol. 2006 Feb;59(2):388-93. doi: 10.1002/ana.20731. Ann Neurol. 2006. PMID: 16437559
38 results