142 related articles for article (PubMed ID: 7632092)
1. Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathy.
Campos Y; Arenas J; Cabello A; Gomez-Reino JJ
Ann Rheum Dis; 1995 Jun; 54(6):491-3. PubMed ID: 7632092
[TBL] [Abstract][Full Text] [Related]
2. [Characterization of mitochondrial myopathies through the evaluation of the enzymatic activities involved in energy metabolism].
Pedroso FC; Campello AP; Werneck LC; Klüppel ML
Arq Neuropsiquiatr; 1997 Jun; 55(2):249-57. PubMed ID: 9629385
[TBL] [Abstract][Full Text] [Related]
3. Abnormal carnitine distribution in the muscles of patients with idiopathic inflammatory myopathy.
Arenas J; Gonzalez-Crespo MR; Campos Y; Martin MA; Cabello A; Gomez-Reino JJ
Arthritis Rheum; 1996 Nov; 39(11):1869-74. PubMed ID: 8912509
[TBL] [Abstract][Full Text] [Related]
4. 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
Pediatr Res; 1984 Oct; 18(10):991-9. PubMed ID: 6093035
[TBL] [Abstract][Full Text] [Related]
5. Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain.
Taylor RW; Birch-Machin MA; Bartlett K; Turnbull DM
Biochim Biophys Acta; 1993 Jun; 1181(3):261-5. PubMed ID: 8391327
[TBL] [Abstract][Full Text] [Related]
6. Respiratory chain enzymes in muscle of endurance athletes: effect of L-carnitine.
Huertas R; Campos Y; Díaz E; Esteban J; Vechietti L; Montanari G; D'Iddio S; Corsi M; Arenas J
Biochem Biophys Res Commun; 1992 Oct; 188(1):102-7. PubMed ID: 1329742
[TBL] [Abstract][Full Text] [Related]
7. Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy.
Checcarelli N; Prelle A; Moggio M; Comi G; Bresolin N; Papadimitriou A; Fagiolari G; Bordoni A; Scarlato G
J Neurol Sci; 1994 May; 123(1-2):74-9. PubMed ID: 8064325
[TBL] [Abstract][Full Text] [Related]
8. Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples.
Wiedemann FR; Vielhaber S; Schröder R; Elger CE; Kunz WS
Anal Biochem; 2000 Mar; 279(1):55-60. PubMed ID: 10683230
[TBL] [Abstract][Full Text] [Related]
9. Partial cytochrome oxidase (aa3) deficiency in chronic progressive external ophthalmoplegia. Histochemical and biochemical studies.
Byrne E; Dennett X; Trounce I; Henderson R
J Neurol Sci; 1985 Dec; 71(2-3):257-71. PubMed ID: 2418159
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial function in heart muscle from patients with idiopathic dilated cardiomyopathy.
Jarreta D; Orús J; Barrientos A; Miró O; Roig E; Heras M; Moraes CT; Cardellach F; Casademont J
Cardiovasc Res; 2000 Mar; 45(4):860-5. PubMed ID: 10728411
[TBL] [Abstract][Full Text] [Related]
11. Changes of respiratory chain enzyme activities in growing rat muscle mitochondria.
Wu CM; Lee DH; Hong YC; Wen DW; Chou CF; Chung MT
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994; 35(2):113-8. PubMed ID: 8184686
[TBL] [Abstract][Full Text] [Related]
12. Sarcoid myopathy and mitochondrial respiratory chain defects: clinicopathological, biochemical and molecular biological analyses.
Reichmann H; Schalke B; Seibel P; Naumann M; Toyka K
Neuromuscul Disord; 1995 Jul; 5(4):277-83. PubMed ID: 7580239
[TBL] [Abstract][Full Text] [Related]
13. Depletion of mitochondrial DNA in the liver of an infant with neonatal giant cell hepatitis.
Müller-Höcker J; Muntau A; Schäfer S; Jaksch M; Staudt F; Pongratz D; Taanman JW
Hum Pathol; 2002 Feb; 33(2):247-53. PubMed ID: 11957153
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial DNA deletions in inclusion body myositis.
Oldfors A; Larsson NG; Lindberg C; Holme E
Brain; 1993 Apr; 116 ( Pt 2)():325-36. PubMed ID: 8384916
[TBL] [Abstract][Full Text] [Related]
15. A mitochondrial myopathy with a defective respiratory chain and carnitine deficiency.
Sengers RC; Fischer JC; Trijbels JM; Ruitenbeek W; Stadhouders AM; ter Laak HJ; Jaspar HH
Eur J Pediatr; 1983 Sep; 140(4):332-7. PubMed ID: 6313374
[TBL] [Abstract][Full Text] [Related]
16. Respiratory chain dysfunction in perifascicular muscle fibres in patients with dermatomyositis is associated with mitochondrial DNA depletion.
Hedberg-Oldfors C; Lindgren U; Visuttijai K; Lööf D; Roos S; Thomsen C; Oldfors A
Neuropathol Appl Neurobiol; 2022 Dec; 48(7):e12841. PubMed ID: 35894812
[TBL] [Abstract][Full Text] [Related]
17. Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
Lalani SR; Vladutiu GD; Plunkett K; Lotze TE; Adesina AM; Scaglia F
Arch Neurol; 2005 Feb; 62(2):317-20. PubMed ID: 15710863
[TBL] [Abstract][Full Text] [Related]
18. Enzyme histochemistry of endomyocardial biopsies in idiopathic dilated cardiomyopathy.
Figulla HR; Bardosi A; Dechant K; Kreuzer H
Cardiology; 1991; 78(3):282-90. PubMed ID: 1651162
[TBL] [Abstract][Full Text] [Related]
19. Human skeletal muscle mitochondria in aging: lack of detectable morphological and enzymic defects.
Zucchini C; Pugnaloni A; Pallotti F; Solmi R; Crimi M; Castaldini C; Biagini G; Lenaz G
Biochem Mol Biol Int; 1995 Nov; 37(4):607-16. PubMed ID: 8589633
[TBL] [Abstract][Full Text] [Related]
20. Effects of veratrine on skeletal muscle mitochondria: ultrastructural, cytochemical, and morphometrical studies.
Freitas EM; Fagian MM; da Cruz-Höfling MA
Microsc Res Tech; 2006 Feb; 69(2):108-18. PubMed ID: 16456834
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]