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3. A familial mitochondrial myopathy with central defect in neural transmission. Barron SA; Heffner RR; Zwirecki R Arch Neurol; 1979 Sep; 36(9):553-6. PubMed ID: 224846 [TBL] [Abstract][Full Text] [Related]
4. [A case of oculocraniosomatic neuromuscular disease with "ragged-red" fibers]. Matsubara S; Yasuda A; Komai K; Okumura S; Takamori M Rinsho Shinkeigaku; 1984 Mar; 24(3):221-9. PubMed ID: 6467743 [No Abstract] [Full Text] [Related]
5. Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular disease. Scarlato G; Pellegrini G; Veicsteinas A J Neuropathol Exp Neurol; 1978 Jan; 37(1):1-12. PubMed ID: 619006 [TBL] [Abstract][Full Text] [Related]
6. The mitochondrial myopathies: 9 case reports and a literature review. Fitzsimons RB Clin Exp Neurol; 1981; 17():185-210. PubMed ID: 7346199 [TBL] [Abstract][Full Text] [Related]
7. [Mitochondrial myopathy of progressive external ophthalmoplegia]. Guo YP Zhonghua Bing Li Xue Za Zhi; 1992 Dec; 21(6):358-60. PubMed ID: 1299529 [TBL] [Abstract][Full Text] [Related]
10. Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies. Andreetta F; Tritschler HJ; Schon EA; DiMauro S; Bonilla E J Neurol Sci; 1991 Sep; 105(1):88-92. PubMed ID: 1665507 [TBL] [Abstract][Full Text] [Related]
11. [Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria (author's transl)]. Okamura K; Nagae K; Omae T; Mita T Rinsho Shinkeigaku; 1975 Apr; 15(4):177-83. PubMed ID: 1170056 [No Abstract] [Full Text] [Related]
12. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria. Tamura K; Santa T; Kuroiwa Y Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795 [No Abstract] [Full Text] [Related]
13. Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase. Haginoya K; Miyabayashi S; Iinuma K; Tada K Acta Neuropathol; 1990; 80(6):642-8. PubMed ID: 2177307 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria. Okamura K; Santa T; Nagae K; Omae T J Neurol Sci; 1976 Jan; 27(1):79-91. PubMed ID: 175134 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
19. [Ophthalmoplegia plus and ragged red fibers. Description of a case manifested in childhood]. De Langlade E; Corazza G; Minetti C; Bado M; Venzano V; Chiossi FM Minerva Pediatr; 1983 Nov; 35(22):1117-23. PubMed ID: 6672599 [No Abstract] [Full Text] [Related]