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3. Progressive cerebral poliodystrophy--Alpers' disease. Disorganized giant neuronal mitochondria on electron microscopy. Sandbank U; Lerman P J Neurol Neurosurg Psychiatry; 1972 Dec; 35(6):749-55. PubMed ID: 4647849 [TBL] [Abstract][Full Text] [Related]
4. Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver. Prick MJ; Gabreëls FJ; Renier WO; Trijbels JM; Sengers RC; Slooff JL Arch Neurol; 1981 Dec; 38(12):767-72. PubMed ID: 7316843 [TBL] [Abstract][Full Text] [Related]
5. Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature. Fukuhara N; Tokiguchi S; Shirakawa K; Tsubaki T J Neurol Sci; 1980 Jul; 47(1):117-33. PubMed ID: 6774061 [TBL] [Abstract][Full Text] [Related]
6. Progressive poliodystrophy (Alpers' disease) with a defect in cytochrome aa3 in muscle: a report of two unrelated patients. Prick MJ; Gabreëls FJ; Trijbels JM; Janssen AJ; le Coultre R; van Dam K; Jaspar HH; Ebels EJ; Op de Coul AA Clin Neurol Neurosurg; 1983; 85(1):57-70. PubMed ID: 6303665 [TBL] [Abstract][Full Text] [Related]
8. [Morphological study of muscle fibers stained red by modified Gomori trichrome staining with special reference to smooth red fibers]. Yoshida K Hokkaido Igaku Zasshi; 1997 Mar; 72(2):163-80. PubMed ID: 9145310 [TBL] [Abstract][Full Text] [Related]
9. [Proceedings: Infantile cerebral poliodystrophy (Alper's disease) in an infant with hyperlactacidemia and hepatic pyruvate carboxylase]. David M; Baltassat P; Dinjon B; Lauras B; De Villard R; Tommasi M; Gilly J Arch Fr Pediatr; 1975; 32(6):580. PubMed ID: 1180638 [No Abstract] [Full Text] [Related]
10. Childhood mitochondrial myopathy with ophthalmoplegia. Land JM; Hockaday JM; Hughes JT; Ross BD J Neurol Sci; 1981 Sep; 51(3):371-82. PubMed ID: 7276984 [TBL] [Abstract][Full Text] [Related]
11. Mitochondrial DNA depletion in Alpers syndrome. Tesarova M; Mayr JA; Wenchich L; Hansikova H; Elleder M; Blahova K; Sperl W; Zeman J Neuropediatrics; 2004 Aug; 35(4):217-23. PubMed ID: 15328560 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Mitochondrial myopathy with increased blood lactate and pyruvate levels among siblings in familial thiamine deficiency]. Sato Y; Kaji M; Osame M; Matsuishi T; Itokawa Y Rinsho Shinkeigaku; 1983 Aug; 23(8):668-77. PubMed ID: 6661867 [No Abstract] [Full Text] [Related]
16. Diffuse leukodystrophy with a large-scale mitochondrial DNA deletion. Nakai A; Goto Y; Fujisawa K; Shigematsu Y; Kikawa Y; Konishi Y; Nonaka I; Sudo M Lancet; 1994 Jun; 343(8910):1397-8. PubMed ID: 7910887 [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]