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22. Neuropathy and mitochondrial myopathy. Peyronnard JM; Charron L; Bellavance A; Marchand L Ann Neurol; 1980 Mar; 7(3):262-8. PubMed ID: 6252825 [TBL] [Abstract][Full Text] [Related]
23. Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applications. Johnson MA; Bindoff LA; Turnbull DM Ann Neurol; 1993 Jan; 33(1):28-35. PubMed ID: 8388186 [TBL] [Abstract][Full Text] [Related]
24. Expression of NCAM (neural cell adhesion molecule) in mitochondrial myopathy. Heuss D; Engelhardt A; Göbel H; Neundörfer B Clin Neuropathol; 1995; 14(6):331-6. PubMed ID: 8605739 [TBL] [Abstract][Full Text] [Related]
25. Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration. Sugie H; Hanson R; Rasmussen G; Verity MA J Neurol Neurosurg Psychiatry; 1982 Jun; 45(6):507-12. PubMed ID: 7119813 [TBL] [Abstract][Full Text] [Related]
26. Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers. Challa S; Kanikannan MA; Murthy JM; Bhoompally VR; Surath M Neurol India; 2004 Sep; 52(3):353-8. PubMed ID: 15472426 [TBL] [Abstract][Full Text] [Related]
27. [Ocular myopathy with mitochondrial abnormalities. Observation of a case with histo-enzymologic and ultrastructural examinations]. Mikol F; Mawas E; Mikol J Bull Soc Ophtalmol Fr; 1973 Mar; 73(3):429-37. PubMed ID: 4792541 [No Abstract] [Full Text] [Related]
28. A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line. Pellegrini G; Barbieri S; Moggio M; Cheldi A; Scarlato G; Minetti C Neuropediatrics; 1985 Aug; 16(3):162-6. PubMed ID: 4047349 [TBL] [Abstract][Full Text] [Related]
30. [From muscle to central nervous system: birth and future of the mitochondrial encephalomyopathy concept]. Serratrice G; Baumann N Rev Neurol (Paris); 1991; 147(6-7):413-6. PubMed ID: 1962046 [TBL] [Abstract][Full Text] [Related]
31. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 34-1987. A 30-year-old woman with an ocular motility disturbance, myopathy, and hypocalcemia. N Engl J Med; 1987 Aug; 317(8):493-501. PubMed ID: 3614294 [No Abstract] [Full Text] [Related]
32. Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia. Takei Y; Ikeda S; Yanagisawa N; Takahashi W; Sekiguchi M; Hayashi T Muscle Nerve; 1995 Nov; 18(11):1321-5. PubMed ID: 7565930 [TBL] [Abstract][Full Text] [Related]
34. [Clinico-pathological study of 10 cases with ocular myopathy - with special reference to mitochondrial abnormalities]. Santa T; Hosokawa S; Tamura K; Kuroiwa Y; Okamura K Rinsho Shinkeigaku; 1975 Oct; 15(10):683-93. PubMed ID: 1241341 [No Abstract] [Full Text] [Related]
36. Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy. Egger J; Lake BD; Wilson J Arch Dis Child; 1981 Oct; 56(10):741-52. PubMed ID: 7305411 [TBL] [Abstract][Full Text] [Related]
37. Variability of mitochondrial cytochemistry in human neuromuscular diseases. Shah A; Sahgal V; Sahgal S; Subramani V; Kochar H J Submicrosc Cytol Pathol; 1988 Apr; 20(2):287-95. PubMed ID: 3395968 [TBL] [Abstract][Full Text] [Related]
38. [Myotubular or centronuclear myopathy; report of a case and review of the literature]. Pereira de Sousa R; Miranda D; Perpetuo FO; Campos GB; Vuletin JC Arq Neuropsiquiatr; 1977 Sep; 35(3):247-59. PubMed ID: 901263 [TBL] [Abstract][Full Text] [Related]