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

Year Number of Results
1955 1
1967 1
1983 1
1985 1
1986 2
1992 1
1994 1
1995 4
1996 4
1997 7
1998 4
1999 7
2001 7
2002 7
2003 2
2004 15
2005 14
2006 24
2007 16
2008 6
2009 8
2010 8
2011 10
2012 6
2013 6
2014 3
2015 6
2017 5
2018 8
2019 5
2020 6
2021 5
2022 3
2023 4
2024 0

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Similar articles for PMID: 17568014

197 results

Results by year

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Page 1
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
Charles P, Camuzat A, Benammar N, Sellal F, Destée A, Bonnet AM, Lesage S, Le Ber I, Stevanin G, Dürr A, Brice A; French Parkinson's Disease Genetic Study Group. Charles P, et al. Neurology. 2007 Nov 20;69(21):1970-5. doi: 10.1212/01.wnl.0000269323.21969.db. Epub 2007 Jun 13. Neurology. 2007. PMID: 17568014
SCA2 may present as levodopa-responsive parkinsonism.
Payami H, Nutt J, Gancher S, Bird T, McNeal MG, Seltzer WK, Hussey J, Lockhart P, Gwinn-Hardy K, Singleton AA, Singleton AB, Hardy J, Farrer M. Payami H, et al. Mov Disord. 2003 Apr;18(4):425-9. doi: 10.1002/mds.10375. Mov Disord. 2003. PMID: 12671950
Complex phenotypes in an Indian family with homozygous SCA2 mutations.
Ragothaman M, Sarangmath N, Chaudhary S, Khare V, Mittal U, Sharma S, Komatireddy S, Chakrabarti S, Mukerji M, Juyal RC, Thelma BK, Muthane UB. Ragothaman M, et al. Ann Neurol. 2004 Jan;55(1):130-3. doi: 10.1002/ana.10815. Ann Neurol. 2004. PMID: 14705123
Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
Furtado S, Payami H, Lockhart PJ, Hanson M, Nutt JG, Singleton AA, Singleton A, Bower J, Utti RJ, Bird TD, de la Fuente-Fernandez R, Tsuboi Y, Klimek ML, Suchowersky O, Hardy J, Calne DB, Wszolek ZK, Farrer M, Gwinn-Hardy K, Stoessl AJ. Furtado S, et al. Mov Disord. 2004 Jun;19(6):622-9. doi: 10.1002/mds.20074. Mov Disord. 2004. PMID: 15197699 Review.
197 results