138 related articles for article (PubMed ID: 9629385)
1. [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]
2. 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]
3. 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]
4. Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins.
Hall RE; Henriksson KG; Lewis SF; Haller RG; Kennaway NG
J Clin Invest; 1993 Dec; 92(6):2660-6. PubMed ID: 8254022
[TBL] [Abstract][Full Text] [Related]
5. Variability in the activity of respiratory chain enzymes in mitochondrial myopathies.
Koga Y; Nonaka I; Sunohara N; Yamanaka R; Kumagai K
Acta Neuropathol; 1988; 76(2):135-41. PubMed ID: 2841822
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. AZT-induced mitochondrial myopathy.
Tomelleri G; Tonin P; Spadaro M; Tilia G; Orrico D; Barelli A; Bonetti B; Monaco S; Salviati A; Morocutti C
Ital J Neurol Sci; 1992 Dec; 13(9):723-8. PubMed ID: 1336487
[TBL] [Abstract][Full Text] [Related]
9. [Cytochrome oxidase and succinate dehydrogenase double staining method in mitochondrial myopathy].
Gao M; Liu W; Chen Y; Zhang W
Zhonghua Bing Li Xue Za Zhi; 2015 Mar; 44(3):208-9. PubMed ID: 26268760
[No Abstract] [Full Text] [Related]
10. On the stability of key enzymes of energy metabolism in muscle biopsies.
Pache T; Reichmann H
Enzyme; 1990; 43(4):183-7. PubMed ID: 1966286
[TBL] [Abstract][Full Text] [Related]
11. Abnormal platelet mitochondrial function in patients affected by migraine with and without aura.
Sangiorgi S; Mochi M; Riva R; Cortelli P; Monari L; Pierangeli G; Montagna P
Cephalalgia; 1994 Feb; 14(1):21-3. PubMed ID: 8200018
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion.
Bodnar AG; Cooper JM; Holt IJ; Leonard JV; Schapira AH
Am J Hum Genet; 1993 Sep; 53(3):663-9. PubMed ID: 8394647
[TBL] [Abstract][Full Text] [Related]
16. Biochemical evaluation of mitochondrial respiratory chain enzymes in canine skeletal muscle.
Wakshlag JJ; Cooper BJ; Wakshlag RR; Kallfelz FA; Barr SC; Nydam DV; Dimauro S
Am J Vet Res; 2004 Apr; 65(4):480-4. PubMed ID: 15077691
[TBL] [Abstract][Full Text] [Related]
17. Myoclonus epilepsy with ragged red fibers and multiple mtDNA deletions.
Blumenthal DT; Shanske S; Schochet SS; Santorelli FM; DiMauro S; Jaynesm M; Bodensteiner J
Neurology; 1998 Feb; 50(2):524-5. PubMed ID: 9484389
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Succinate dehydrogenase deficiency.
Vladutiu GD; Heffner RR
Arch Pathol Lab Med; 2000 Dec; 124(12):1755-8. PubMed ID: 11100052
[TBL] [Abstract][Full Text] [Related]
20. Cytochrome c oxidase deficiency in zidovudine myopathy affects perifascicular muscle fibres and arterial smooth muscle cells.
Chariot P; Le Maguet F; Authier FJ; Labes D; Poron F; Gherardi R
Neuropathol Appl Neurobiol; 1995 Dec; 21(6):540-7. PubMed ID: 8745244
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
