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2. [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]
3. [Mitochondrial myopathies and encephalomyopathies. Neuromuscular and central nervous system diseases caused by defects in mitochondrial oxidative metabolism]. Siemes H Monatsschr Kinderheilkd; 1985 Nov; 133(11):798-805. PubMed ID: 3935918 [TBL] [Abstract][Full Text] [Related]
7. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency. Kobayashi M; Morishita H; Sugiyama N; Yokochi K; Nakano M; Wada Y; Hotta Y; Terauchi A; Nonaka I J Inherit Metab Dis; 1986; 9(3):301-4. PubMed ID: 3099078 [No Abstract] [Full Text] [Related]
8. MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature. van Hellenberg Hubar JL; Gabreëls FJ; Ruitenbeek W; Sengers RC; Renier WO; Thijssen HO; ter Laak HJ Neuropediatrics; 1991 Feb; 22(1):10-4. PubMed ID: 1903852 [TBL] [Abstract][Full Text] [Related]
10. [Myasthenic form of a metabolic myopathy with dystrophic changes due to storage and symptoms resembling McArdle's syndrome (a case report)]. Wagner A; Zett W Psychiatr Neurol Med Psychol (Leipz); 1971 Nov; 23(11):650-7. PubMed ID: 5291479 [No Abstract] [Full Text] [Related]
11. A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness. Hackett TN; Bray PF; Ziter FA; Nyhan WL; Creer KM J Pediatr; 1973 Sep; 83(3):426-31. PubMed ID: 4725145 [No Abstract] [Full Text] [Related]
14. [Ophthalmoplegia plus. On nosologic, biochemical, morphologic and computer tomographic aspects of the oculocraniosomatic syndrome]. Lössner J; Lehmann W; Kühn HJ; Ziegan J; Brehme M Psychiatr Neurol Med Psychol Beih; 1983; 29():184-95. PubMed ID: 6415699 [No Abstract] [Full Text] [Related]
15. [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. Alexia without agraphia or hemianopia. Caffarra P Eur Neurol; 1987; 27(2):65-71. PubMed ID: 3622584 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Alexia without agraphia. Anatomical basis and physiopathological mechanisms]. Delreux V; Kevers L; Callewaert A Acta Neurol Belg; 1987; 87(5):267-72. PubMed ID: 3434198 [TBL] [Abstract][Full Text] [Related]
19. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome. Pavlakis SG; Phillips PC; DiMauro S; De Vivo DC; Rowland LP Ann Neurol; 1984 Oct; 16(4):481-8. PubMed ID: 6093682 [TBL] [Abstract][Full Text] [Related]
20. [A case of mitochondrial encephalomyopathy with myoclonic attacks, hyper-lactic-pyruvic acidemia, and decreased activities of complex II and cytochrome c oxidase]. Harigaya Y; Shoji M; Okamoto K; Hirai S; Sato T Rinsho Shinkeigaku; 1988 Jan; 28(1):24-31. PubMed ID: 2838211 [No Abstract] [Full Text] [Related] [Next] [New Search]