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Journal Abstract Search
182 related items for PubMed ID: 2826704
1. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration. Yamamoto M, Sato T, Anno M, Ujike H, Takemoto M. J Neurol Neurosurg Psychiatry; 1987 Nov; 50(11):1475-81. PubMed ID: 2826704 [Abstract] [Full Text] [Related]
2. A case of mitochondrial myopathy, encephalopathy and lactic acidosis due to cytochrome c oxidase deficiency with neurogenic muscular changes. Jinnai K, Yamada H, Kanda F, Masui Y, Tanaka M, Ozawa T, Fujita T. Eur Neurol; 1990 Nov; 30(1):56-60. PubMed ID: 2153548 [Abstract] [Full Text] [Related]
7. Clinical improvement after administration of coenzyme Q10 in a patient with mitochondrial encephalomyopathy. Goda S, Hamada T, Ishimoto S, Kobayashi T, Goto I, Kuroiwa Y. J Neurol; 1987 Jan; 234(1):62-3. PubMed ID: 3819789 [Abstract] [Full Text] [Related]
8. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation. Goto Y, Horai S, Matsuoka T, Koga Y, Nihei K, Kobayashi M, Nonaka I. Neurology; 1992 Mar; 42(3 Pt 1):545-50. PubMed ID: 1549215 [Abstract] [Full Text] [Related]
9. [An autopsy case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episode)]. Ohara S, Ohama E, Ikuta F, Nishizawa M, Kuwabara T. Rinsho Shinkeigaku; 1988 Mar; 28(3):303-10. PubMed ID: 3402137 [No Abstract] [Full Text] [Related]
10. [A case of mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS)--treatment with coenzyme Q10 and idebenone]. Ihara Y, Namba R, Kuroda S. Rinsho Shinkeigaku; 1988 Jan; 28(1):62-6. PubMed ID: 3383514 [No Abstract] [Full Text] [Related]
11. An experimental model of mitochondrial myopathy: germanium-induced myopathy and coenzyme Q10 administration. Wu CM, Matsuoka T, Takemitsu M, Goto Y, Nonaka I. Muscle Nerve; 1992 Nov; 15(11):1258-64. PubMed ID: 1488063 [Abstract] [Full Text] [Related]
12. Disproportionate deficiency of iron-sulfur clusters and subunits of complex I in mitochondrial encephalomyopathy. Ichiki T, Tanaka M, Kobayashi M, Sugiyama N, Suzuki H, Nishikimi M, Ohnishi T, Nonaka I, Wada Y, Ozawa T. Pediatr Res; 1989 Feb; 25(2):194-201. PubMed ID: 2493147 [Abstract] [Full Text] [Related]
13. Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency. Koga Y, Nonaka I, Kobayashi M, Tojyo M, Nihei K. Ann Neurol; 1988 Dec; 24(6):749-56. PubMed ID: 3144939 [Abstract] [Full Text] [Related]
14. Coenzyme Q 10 improves lactic acidosis, strokelike episodes, and epilepsy in a patient with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes). Berbel-Garcia A, Barbera-Farre JR, Etessam JP, Salio AM, Cabello A, Gutierrez-Rivas E, Campos Y. Clin Neuropharmacol; 2004 Dec; 27(4):187-91. PubMed ID: 15319706 [Abstract] [Full Text] [Related]
15. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Report of an autopsy. Hamazaki S, Okada S, Kusaka H, Fujii T, Okuno T, Kashu I, Midorikawa O. Acta Pathol Jpn; 1989 Sep; 39(9):599-606. PubMed ID: 2596299 [Abstract] [Full Text] [Related]
16. MELAS of infantile onset: mitochondrial angiopathy or cytopathy? Fujii T, Okuno T, Ito M, Mutoh K, Horiguchi Y, Tashiro H, Mikawa H. J Neurol Sci; 1991 May; 103(1):37-41. PubMed ID: 1865230 [Abstract] [Full Text] [Related]
17. [Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy]. Márquez C, Bautista J, Arenas J, Segura D, Chinchón I, Rafel E, Campos Y, Huerta R. Neurologia; 1991 May; 6(5):185-7. PubMed ID: 1908255 [Abstract] [Full Text] [Related]
18. Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain. Kennaway NG, Buist NR, Darley-Usmar VM, Papadimitriou A, Dimauro S, Kelley RI, Capaldi RA, Blank NK, D'Agostino A. Pediatr Res; 1984 Oct; 18(10):991-9. PubMed ID: 6093035 [Abstract] [Full Text] [Related]
19. [A case of mitochondrial encephalomyopathy--Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS)]. Ihara Y, Namba R, Demiya M, Matsumoto T, Shirabe T. Rinsho Shinkeigaku; 1987 Aug; 27(8):969-75. PubMed ID: 3690923 [No Abstract] [Full Text] [Related]