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

Year Number of Results
1977 1
1983 2
1984 3
1985 1
1987 3
1988 2
1990 2
1991 2
1992 1
1993 8
1994 2
1996 4
1997 8
1998 2
1999 5
2000 7
2001 6
2002 3
2003 4
2004 4
2005 2
2006 5
2007 1
2008 1
2009 3
2010 4
2011 4
2013 3
2014 2
2015 1
2016 1
2017 2
2018 1
2022 1
2024 0

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92 results

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Page 1
Mitochondrial disorders.
Schapira AH. Schapira AH. Curr Opin Neurol. 2000 Oct;13(5):527-32. doi: 10.1097/00019052-200010000-00004. Curr Opin Neurol. 2000. PMID: 11073358 Review.
Mitochondrial myopathies.
DiMauro S, Bonilla E, Zeviani M, Servidei S, DeVivo DC, Schon EA. DiMauro S, et al. J Inherit Metab Dis. 1987;10 Suppl 1:113-28. doi: 10.1007/BF01812852. J Inherit Metab Dis. 1987. PMID: 2824920 Review.
Mitochondrial encephalomyopathies.
DiMauro S, Moraes CT. DiMauro S, et al. Arch Neurol. 1993 Nov;50(11):1197-208. doi: 10.1001/archneur.1993.00540110075008. Arch Neurol. 1993. PMID: 8215979 Review.
Human cytochrome oxidase deficiency.
Robinson BH. Robinson BH. Pediatr Res. 2000 Nov;48(5):581-5. doi: 10.1203/00006450-200011000-00004. Pediatr Res. 2000. PMID: 11044474 Review.
Defects in the biosynthesis of mitochondrial heme c and heme a in yeast and mammals.
Moraes CT, Diaz F, Barrientos A. Moraes CT, et al. Biochim Biophys Acta. 2004 Dec 6;1659(2-3):153-9. doi: 10.1016/j.bbabio.2004.09.002. Biochim Biophys Acta. 2004. PMID: 15576047 Free article. Review.
COX10 and COX15 are two genes, initially identified in Saccharomyces cerevisiae that have been found to cause infantile cytochrome c oxidase deficiency in humans. They participate in the farnesylation and hydroxylation of heme b, steps that are necessa …
COX10 and COX15 are two genes, initially identified in Saccharomyces cerevisiae that have been found to cause infantile cytochrome …
Mitochondrial dysfunction in myofibrillar myopathy.
Vincent AE, Grady JP, Rocha MC, Alston CL, Rygiel KA, Barresi R, Taylor RW, Turnbull DM. Vincent AE, et al. Neuromuscul Disord. 2016 Oct;26(10):691-701. doi: 10.1016/j.nmd.2016.08.004. Epub 2016 Aug 10. Neuromuscul Disord. 2016. PMID: 27618136 Free PMC article.
92 results