164 related articles for article (PubMed ID: 2177405)
21. Mitochondrial complex I deficiency in Parkinson's disease.
Schapira AH; Cooper JM; Dexter D; Clark JB; Jenner P; Marsden CD
J Neurochem; 1990 Mar; 54(3):823-7. PubMed ID: 2154550
[TBL] [Abstract][Full Text] [Related]
22. [Pure mitochondrial myopathy].
Murakami N; Sakuta R
Ryoikibetsu Shokogun Shirizu; 2001; (36):186-9. PubMed ID: 11596366
[No Abstract] [Full Text] [Related]
23. Human mitochondrial respiratory chain deficiencies.
Morgan-Hughes JA; Schapira AH; Cooper JM; Hayes DJ; Clark JB
Aust Paediatr J; 1988; 24 Suppl 1():55-7. PubMed ID: 2849394
[TBL] [Abstract][Full Text] [Related]
24. Development of mitochondrial respiratory-chain complexes in neonatal rat brain.
Almeida A; Bates TE; Clark JB
Biochem Soc Trans; 1994 Nov; 22(4):409S. PubMed ID: 7698431
[No Abstract] [Full Text] [Related]
25. Inborn errors of complex II--unusual human mitochondrial diseases.
Rustin P; Rötig A
Biochim Biophys Acta; 2002 Jan; 1553(1-2):117-22. PubMed ID: 11803021
[TBL] [Abstract][Full Text] [Related]
26. The mitochondrial electron transport and oxidative phosphorylation system.
Hatefi Y
Annu Rev Biochem; 1985; 54():1015-69. PubMed ID: 2862839
[No Abstract] [Full Text] [Related]
27. New insights, ideas and unanswered questions concerning iron-sulfur clusters in mitochondria.
Beinert H; Albracht SP
Biochim Biophys Acta; 1982 Dec; 683(3-4):245-77. PubMed ID: 6297553
[No Abstract] [Full Text] [Related]
28. Effect of endogenous ubiquinone on the interaction of exogenous Ubiquinone-1 with the respiratory chain of bovine heart mitochondria.
Cabrini L; Landi L; Pasquali P; Lenaz G
Arch Biochem Biophys; 1981 Apr; 208(1):11-9. PubMed ID: 6789771
[No Abstract] [Full Text] [Related]
29. Aerobic performance and oxygen free-radicals.
Benzi G
J Sports Med Phys Fitness; 1993 Sep; 33(3):205-22. PubMed ID: 8107472
[No Abstract] [Full Text] [Related]
30. Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies.
Tanaka M; Nishikimi M; Suzuki H; Ozawa T; Koga Y; Nonaka I
Biochem Int; 1987 Mar; 14(3):525-30. PubMed ID: 2884999
[TBL] [Abstract][Full Text] [Related]
31. [A case of mitochondrial encephalomyopathy with myoclonic attacks, hyper-lactic-pyruvic acidemia, and decreased activities of complex II and cytochrome c oxidase].
Harigaya Y; Shoji M; Okamoto K; Hirai S; Sato T
Rinsho Shinkeigaku; 1988 Jan; 28(1):24-31. PubMed ID: 2838211
[No Abstract] [Full Text] [Related]
32. [Clinical and biochemical approach to mitochondrial cytopathy--defects of the respiratory chain].
Kobayashi M
No To Hattatsu; 1987 Mar; 19(2):132-9. PubMed ID: 3030379
[No Abstract] [Full Text] [Related]
33. Analysis of mitochondrial antigens reveals inner membrane succinate dehydrogenase flavoprotein subunit as autoantigen to antibodies in anti-M7 sera.
Cicek G; Schiltz E; Hess D; Staiger J; Brandsch R
Clin Exp Immunol; 2002 Apr; 128(1):83-7. PubMed ID: 11982594
[TBL] [Abstract][Full Text] [Related]
34. Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines.
Trounce IA; Kim YL; Jun AS; Wallace DC
Methods Enzymol; 1996; 264():484-509. PubMed ID: 8965721
[No Abstract] [Full Text] [Related]
35. Structures and proton-pumping strategies of mitochondrial respiratory enzymes.
Schultz BE; Chan SI
Annu Rev Biophys Biomol Struct; 2001; 30():23-65. PubMed ID: 11340051
[TBL] [Abstract][Full Text] [Related]
36. Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxia.
Taylor RW; Birch-Machin MA; Schaefer J; Taylor L; Shakir R; Ackrell BA; Cochran B; Bindoff LA; Jackson MJ; Griffiths P; Turnbull DM
Ann Neurol; 1996 Feb; 39(2):224-32. PubMed ID: 8967754
[TBL] [Abstract][Full Text] [Related]
37. [A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy].
Ohnishi A; Nakano S; Hashimoto T; Tsuji S; Murai Y
Rinsho Shinkeigaku; 1988 Jan; 28(1):107-11. PubMed ID: 2838209
[No Abstract] [Full Text] [Related]
38. The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation system.
Morgan-Hughes JA; Cooper JM; Schapira AH; Hayes DJ; Clark JB
Electroencephalogr Clin Neurophysiol Suppl; 1987; 39():103-14. PubMed ID: 2888641
[No Abstract] [Full Text] [Related]
39. Molecular basis of mitochondrial myopathies.
Lancet; 1988 Apr; 1(8590):884-5. PubMed ID: 2895390
[No Abstract] [Full Text] [Related]
40. Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
Niemann S; Müller U
Nat Genet; 2000 Nov; 26(3):268-70. PubMed ID: 11062460
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
