Similar articles for PMID: 6093035

Year	Number of Results
1941	1
1961	1
1967	1
1968	1
1969	1
1970	1
1976	1
1978	1
1979	1
1980	4
1981	5
1982	3
1983	10
1984	11
1985	5
1986	8
1987	11
1988	13
1989	8
1990	11
1991	9
1992	4
1993	7
1994	5
1995	8
1996	4
1997	5
1998	3
1999	2
2000	2
2001	4
2002	4
2003	2
2004	2
2005	1
2007	1
2009	1
2010	1
2011	1
2015	1
2016	1
2017	2
2018	1
2019	2
2020	3
2021	1
2022	3
2023	4
2024	1

1

Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.

Kennaway NG, Buist NR, Darley-Usmar VM, Papadimitriou A, Dimauro S, Kelley RI, Capaldi RA, Blank NK, D'Agostino A. Kennaway NG, et al. Pediatr Res. 1984 Oct;18(10):991-9. doi: 10.1203/00006450-198410000-00017. Pediatr Res. 1984. PMID: 6093035

2

Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.

Darley-Usmar VM, Kennaway NG, Buist NR, Capaldi RA. Darley-Usmar VM, et al. Proc Natl Acad Sci U S A. 1983 Aug;80(16):5103-6. doi: 10.1073/pnas.80.16.5103. Proc Natl Acad Sci U S A. 1983. PMID: 6308671 Free PMC article.

3

Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase.

Behbehani AW, Goebel H, Osse G, Gabriel M, Langenbeck U, Berden J, Berger R, Schutgens RB. Behbehani AW, et al. Eur J Pediatr. 1984 Nov;143(1):67-71. doi: 10.1007/BF00442753. Eur J Pediatr. 1984. PMID: 6096151

4

Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis.

Moreadith RW, Batshaw ML, Ohnishi T, Kerr D, Knox B, Jackson D, Hruban R, Olson J, Reynafarje B, Lehninger AL. Moreadith RW, et al. J Clin Invest. 1984 Sep;74(3):685-97. doi: 10.1172/JCI111484. J Clin Invest. 1984. PMID: 6432847 Free PMC article.

5

Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.

Morgan-Hughes JA, Hayes DJ, Cooper M, Clark JB. Morgan-Hughes JA, et al. Biochem Soc Trans. 1985 Aug;13(4):648-50. doi: 10.1042/bst0130648. Biochem Soc Trans. 1985. PMID: 2993076 No abstract available.

6

Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy.

Hoppel CL, Kerr DS, Dahms B, Roessmann U. Hoppel CL, et al. J Clin Invest. 1987 Jul;80(1):71-7. doi: 10.1172/JCI113066. J Clin Invest. 1987. PMID: 3110216 Free PMC article.

7

A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity.

Morgan-Hughes JA, Darveniza P, Landon DN, Land JM, Clark JB. Morgan-Hughes JA, et al. J Neurol Sci. 1979 Sep;43(1):27-46. doi: 10.1016/0022-510x(79)90071-6. J Neurol Sci. 1979. PMID: 521828

8

Extensive defects of mitochondrial electron-transfer chain in muscular cytochrome c oxidase deficiency.

Tanaka M, Miyabayashi S, Nishikimi M, Suzuki H, Shimomura Y, Ito K, Narisawa K, Tada K, Ozawa T. Tanaka M, et al. Pediatr Res. 1988 Oct;24(4):447-54. doi: 10.1203/00006450-198810000-00006. Pediatr Res. 1988. PMID: 2845344

9

Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency.

DiMauro S, Mendell JR, Sahenk Z, Bachman D, Scarpa A, Scofield RM, Reiner C. DiMauro S, et al. Neurology. 1980 Aug;30(8):795-804. doi: 10.1212/wnl.30.8.795. Neurology. 1980. PMID: 6251406

10

Human mitochondrial respiratory chain deficiencies.

Morgan-Hughes JA, Schapira AH, Cooper JM, Hayes DJ, Clark JB. Morgan-Hughes JA, et al. Aust Paediatr J. 1988;24 Suppl 1:55-7. Aust Paediatr J. 1988. PMID: 2849394 Review.

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