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Results by year

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

Year Number of Results
1965 1
1966 1
1968 2
1970 1
1971 1
1974 1
1975 1
1977 1
1980 1
1990 1
1991 1
1993 2
1995 1
1997 1
1998 2
1999 3
2000 2
2001 6
2002 5
2003 5
2004 5
2005 15
2006 16
2007 13
2008 17
2009 17
2010 23
2011 26
2012 16
2013 15
2014 19
2015 11
2016 15
2017 12
2018 7
2019 7
2020 5
2021 5
2022 4
2023 3
2024 1

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Similar articles for PMID: 15929042

255 results

Results by year

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Page 1
POLG mutations and Alpers syndrome.
Davidzon G, Mancuso M, Ferraris S, Quinzii C, Hirano M, Peters HL, Kirby D, Thorburn DR, DiMauro S. Davidzon G, et al. Ann Neurol. 2005 Jun;57(6):921-3. doi: 10.1002/ana.20498. Ann Neurol. 2005. PMID: 15929042
POLG1 mutations associated with progressive encephalopathy in childhood.
Kollberg G, Moslemi AR, Darin N, Nennesmo I, Bjarnadottir I, Uvebrant P, Holme E, Melberg A, Tulinius M, Oldfors A. Kollberg G, et al. J Neuropathol Exp Neurol. 2006 Aug;65(8):758-68. doi: 10.1097/01.jnen.0000229987.17548.6e. J Neuropathol Exp Neurol. 2006. PMID: 16896309
Molecular diagnosis of Alpers syndrome.
Nguyen KV, Sharief FS, Chan SS, Copeland WC, Naviaux RK. Nguyen KV, et al. J Hepatol. 2006 Jul;45(1):108-16. doi: 10.1016/j.jhep.2005.12.026. Epub 2006 Feb 20. J Hepatol. 2006. PMID: 16545482
POLG mutations in Alpers syndrome.
Nguyen KV, Østergaard E, Ravn SH, Balslev T, Danielsen ER, Vardag A, McKiernan PJ, Gray G, Naviaux RK. Nguyen KV, et al. Neurology. 2005 Nov 8;65(9):1493-5. doi: 10.1212/01.wnl.0000182814.55361.70. Epub 2005 Sep 21. Neurology. 2005. PMID: 16177225
255 results