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

Year Number of Results
1907 1
1981 1
1983 1
1986 1
1988 1
1991 1
1992 2
1993 1
1994 2
1995 2
1996 1
1997 4
1998 5
1999 7
2000 6
2001 5
2002 6
2003 4
2004 8
2005 8
2006 4
2007 4
2008 6
2009 4
2010 4
2011 7
2012 6
2013 4
2014 3
2015 3
2016 3
2017 5
2018 8
2019 4
2020 4
2021 3
Text availability
Article attribute
Article type
Publication date

Similar articles for PMID: 12612282

129 results
Results by year
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Page 1
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
Mitochondrial DNA depletion in Alpers syndrome.
Tesarova M, Mayr JA, Wenchich L, Hansikova H, Elleder M, Blahova K, Sperl W, Zeman J. Tesarova M, et al. Neuropediatrics. 2004 Aug;35(4):217-23. doi: 10.1055/s-2004-821081. Neuropediatrics. 2004. PMID: 15328560
129 results
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