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46. Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA. Holt IJ; Harding AE; Cooper JM; Schapira AH; Toscano A; Clark JB; Morgan-Hughes JA Ann Neurol; 1989 Dec; 26(6):699-708. PubMed ID: 2604380 [TBL] [Abstract][Full Text] [Related]
47. Progressive external ophthalmoplegia. Evidence for a generalised mitochondrial disease with a defect in pyruvate metabolism. Reske-Nielsen E; Lou HC; Lowes M Acta Ophthalmol (Copenh); 1976 Oct; 54(5):553-73. PubMed ID: 185877 [TBL] [Abstract][Full Text] [Related]
48. Ophthalmoplegia-plus. Its occurrence with periventricular diffuse low density on computed tomography scan. Okamoto T; Mizuno K; Iida M; Sobue I; Mukoyama M Arch Neurol; 1981 Jul; 38(7):423-6. PubMed ID: 7247764 [TBL] [Abstract][Full Text] [Related]
49. Electroencephalographic findings in patients with chronic progressive external ophthalmoplegia. Tartara A; Manni R; Scelsi R; Piccolo G; Cosi V Ital J Neurol Sci; 1983 Dec; 4(4):459-62. PubMed ID: 6674247 [TBL] [Abstract][Full Text] [Related]
50. Paracrystalline arrays in mitochondria following ageing of mitochondria in situ. Cheah KS; Cheah AM; Voyle CA J Bioenerg; 1973 Apr; 4(3):383-9. PubMed ID: 4354963 [No Abstract] [Full Text] [Related]
51. Hypometabolism of nonthyroid origin in oculocraniosomatic neuromuscular disease. Krieger I; Hart Z Monogr Hum Genet; 1978; 10():192-9. PubMed ID: 723893 [No Abstract] [Full Text] [Related]
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