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

Year Number of Results
1981 2
1982 1
1983 1
1984 2
1985 2
1986 3
1987 1
1988 2
1989 3
1990 4
1991 7
1992 5
1993 12
1994 14
1995 10
1996 11
1997 9
1998 12
1999 22
2000 8
2001 4
2002 8
2003 7
2004 12
2005 4
2006 2
2007 6
2008 7
2009 5
2010 2
2011 1
2012 2
2013 1
2014 1
2016 2
2018 1
2019 3
2020 2
2021 2
2022 1
2023 1
2024 0

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197 results

Results by year

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Page 1
Detection of mitochondrial DNA (mtDNA) mutations.
Naini A, Gilkerson R, Shanske S, Pang J. Naini A, et al. Among authors: shanske s. Methods Cell Biol. 2020;155:383-400. doi: 10.1016/bs.mcb.2019.11.009. Epub 2019 Dec 2. Methods Cell Biol. 2020. PMID: 32183969 Free PMC article.
Detection of mutations in mtDNA.
Naini A, Shanske S. Naini A, et al. Among authors: shanske s. Methods Cell Biol. 2007;80:437-63. doi: 10.1016/S0091-679X(06)80022-1. Methods Cell Biol. 2007. PMID: 17445708 Review. No abstract available.
Metabolic myopathies.
DiMauro S, Miranda AF, Sakoda S, Schon EA, Servidei S, Shanske S, Zeviani M. DiMauro S, et al. Among authors: shanske s. Am J Med Genet. 1986 Dec;25(4):635-51. doi: 10.1002/ajmg.1320250406. Am J Med Genet. 1986. PMID: 2878616
The other human genome.
Shanske AL, Shanske S, DiMauro S. Shanske AL, et al. Among authors: shanske s. Arch Pediatr Adolesc Med. 2001 Nov;155(11):1210-6. doi: 10.1001/archpedi.155.11.1210. Arch Pediatr Adolesc Med. 2001. PMID: 11695929 Review.
Mitochondrial encephalomyopathies.
DiMauro S, Zeviani M, Moraes CT, Nakase H, Rizzuto R, Lombes A, Shanske S, Schon EA. DiMauro S, et al. Among authors: shanske s. Prog Clin Biol Res. 1989;306:117-28. Prog Clin Biol Res. 1989. PMID: 2544896 Review. No abstract available.
Maternally inherited Leigh syndrome.
Ciafaloni E, Santorelli FM, Shanske S, Deonna T, Roulet E, Janzer C, Pescia G, DiMauro S. Ciafaloni E, et al. Among authors: shanske s. J Pediatr. 1993 Mar;122(3):419-22. doi: 10.1016/s0022-3476(05)83431-6. J Pediatr. 1993. PMID: 8095070
197 results