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Results by year

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

Year Number of Results
1982 2
1983 2
1984 3
1985 1
1987 1
1988 2
1989 7
1990 2
1991 3
1992 7
1993 6
1994 5
1995 8
1996 5
1997 5
1998 7
1999 6
2000 2
2001 1
2002 7
2003 3
2004 1
2005 1
2006 5
2007 1
2008 3
2009 4
2010 2
2011 1
2012 2
2013 5
2014 2
2015 2
2016 2
2017 1
2018 2
2019 5
2020 1
2021 4
2022 5
2023 1
2024 0

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Similar articles for PMID: 8151637

131 results

Results by year

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Page 1
Mitochondrial genome analysis in Kearns-Sayre syndrome.
Lertrit P, Atchaneeyasakul L, Devahastin V, Saechan V, Sangruchi T, Neungton N, Lekhakula S. Lertrit P, et al. Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:162-5. Southeast Asian J Trop Med Public Health. 1995. PMID: 8629098
Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromes.
Gustafson MA, McCormick EM, Perera L, Longley MJ, Bai R, Kong J, Dulik M, Shen L, Goldstein AC, McCormack SE, Laskin BL, Leroy BP, Ortiz-Gonzalez XR, Ellington MG, Copeland WC, Falk MJ. Gustafson MA, et al. PLoS One. 2019 Sep 3;14(9):e0221829. doi: 10.1371/journal.pone.0221829. eCollection 2019. PLoS One. 2019. PMID: 31479473 Free PMC article.
131 results