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24. Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia. Turnbull DM; Johnson MA; Dick DJ; Cartlidge NE; Sherratt HS J Neurol Sci; 1985 Aug; 70(1):93-100. PubMed ID: 2995595 [TBL] [Abstract][Full Text] [Related]
25. Partial deficiency of complexes I and IV of the mitochondrial respiratory chain in skeletal muscle of two patients with mitochondrial myopathy. Bleistein J; Zierz S J Neurol; 1989 May; 236(4):218-22. PubMed ID: 2547913 [TBL] [Abstract][Full Text] [Related]
26. Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiency. Servidei S; Lazaro RP; Bonilla E; Barron KD; Zeviani M; DiMauro S Neurology; 1987 Jan; 37(1):58-63. PubMed ID: 3025775 [TBL] [Abstract][Full Text] [Related]
27. Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase. Roodhooft AM; Van Acker KJ; Martin JJ; Ceuterick C; Scholte HR; Luyt-Houwen IE Neuropediatrics; 1986 Nov; 17(4):221-6. PubMed ID: 3027606 [TBL] [Abstract][Full Text] [Related]
28. A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia. Johnson MA; Turnbull DM; Dick DJ; Sherratt HS J Neurol Sci; 1983 Jul; 60(1):31-53. PubMed ID: 6308177 [TBL] [Abstract][Full Text] [Related]
29. A morphometric study of muscle mitochondria in cytochrome c oxidase deficiency. Chung S; Nonaka I J Neurol Sci; 1988 Feb; 83(2-3):269-82. PubMed ID: 2833575 [TBL] [Abstract][Full Text] [Related]
30. Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts. Telerman-Toppet N; Biarent D; Bouton JM; de Meirleir L; Elmer C; Noel S; Vamos E; DiMauro S J Inherit Metab Dis; 1992; 15(3):323-6. PubMed ID: 1383604 [No Abstract] [Full Text] [Related]
31. Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient. Zeviani M; Nonaka I; Bonilla E; Okino E; Moggio M; Jones S; DiMauro S Ann Neurol; 1985 Apr; 17(4):414-7. PubMed ID: 2988412 [TBL] [Abstract][Full Text] [Related]
32. [Delayed manifestation of mitochondrial myopathy--complex I and IV deficiency of the mitochondrial respiratory chain with progressive paresis]. Beyenburg S; von Wersebe O; Zierz S Nervenarzt; 1991 Aug; 62(8):506-11. PubMed ID: 1658669 [TBL] [Abstract][Full Text] [Related]
33. Cytochrome oxidase deficiency affecting the structure of the myofibre and the shape of mitochondrial cristae membrane. Sumegi B; Melegh B; Adamovich K; Trombitas K Clin Chim Acta; 1990 Nov; 192(1):9-18. PubMed ID: 2175684 [TBL] [Abstract][Full Text] [Related]
34. ["Central core" myopathy: report of a case]. Werneck LC; Silvado CE Arq Neuropsiquiatr; 1981 Jun; 39(2):230-6. PubMed ID: 7283803 [TBL] [Abstract][Full Text] [Related]
35. Focal deficiency of cytochrome c oxidase and of mitochondrial ATPase with histochemical evidence of loosely coupled oxidative phosphorylation in a mitochondrial myopathy of a patient with bilateral ptosis. An enzyme histochemical, immunocytochemical and fine structural study. Müller-Höcker J; Stünkel S; Pongratz D; Hübner G J Neurol Sci; 1985; 69(1-2):27-36. PubMed ID: 2989441 [TBL] [Abstract][Full Text] [Related]
36. [A case of familial mitochondrial myopathy associated with peripheral neuropathy and optic atrophy]. Watanabe M; Mizusawa H; Kanazawa I; Nakanisi T Rinsho Shinkeigaku; 1987 Sep; 27(9):1163-6. PubMed ID: 2831006 [No Abstract] [Full Text] [Related]
37. Enzyme activity measured in single muscle fibers in partial cytochrome c oxidase deficiency. Reichmann H Neurology; 1988 Feb; 38(2):244-9. PubMed ID: 2829055 [TBL] [Abstract][Full Text] [Related]
38. Cytochrome c oxidase deficient fibres in the limb muscle and diaphragm of man without muscular disease: an age-related alteration. Müller-Höcker J J Neurol Sci; 1990 Dec; 100(1-2):14-21. PubMed ID: 1965203 [TBL] [Abstract][Full Text] [Related]
39. Evaluation of the hypotonic or floppy infant. Bergen BJ Minn Med; 1985 May; 68(5):341-7. PubMed ID: 4010657 [No Abstract] [Full Text] [Related]
40. Benign congenital hypotonia with uniform type 1 fibers and aspecific ultrastructural changes in the muscle: a case with esophagus involvement. Spagnoli LG; Palmieri G; Bertini E Ital J Neurol Sci; 1985 Sep; 6(3):317-21. PubMed ID: 2933366 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]