These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
106 related articles for article (PubMed ID: 8831249)
1. [Benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency]. Wada H; Nishio H; Nagaki S; Yanagawa H; Imamura A; Yokoyama S; Sano T; Woo M; Matsuo M; Itoh H; Nakamura H No To Hattatsu; 1996 Sep; 28(5):443-7. PubMed ID: 8831249 [TBL] [Abstract][Full Text] [Related]
2. Vascular involvement in benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency. Wada H; Woo M; Nishio H; Nagaki S; Yanagawa H; Imamura A; Yokoyama S; Ohbayashi C; Matsuo M; Itoh H; Nakamura H Brain Dev; 1996; 18(4):263-8. PubMed ID: 8879644 [TBL] [Abstract][Full Text] [Related]
3. Reversible mitochondrial myopathy with cytochrome c oxidase deficiency. Salo MK; Rapola J; Somer H; Pihko H; Koivikko M; Tritschler HJ; DiMauro S Arch Dis Child; 1992 Aug; 67(8):1033-5. PubMed ID: 1325759 [TBL] [Abstract][Full Text] [Related]
4. [Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency: histological and biochemical analysis]. Suzuki M; Sugie H; Tsurui S; Miyamoto R; Sugie Y; Igarashi Y; Kaku H; Fukami S No To Hattatsu; 1989 Nov; 21(6):543-9. PubMed ID: 2553079 [TBL] [Abstract][Full Text] [Related]
5. Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency. DiMauro S; Nicholson JF; Hays AP; Eastwood AB; Papadimitriou A; Koenigsberger R; DeVivo DC Ann Neurol; 1983 Aug; 14(2):226-34. PubMed ID: 6312869 [TBL] [Abstract][Full Text] [Related]
6. [A case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) with progressive cytochrome c oxidase deficiency]. Sumi K; Nagaura T; Itagaki Y; Inui K; Abe J Rinsho Shinkeigaku; 1989 Jul; 29(7):901-8. PubMed ID: 2553313 [TBL] [Abstract][Full Text] [Related]
7. Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement. Figarella-Branger D; Pellissier JF; Scheiner C; Wernert F; Desnuelle C J Neurol Sci; 1992 Mar; 108(1):105-13. PubMed ID: 1320661 [TBL] [Abstract][Full Text] [Related]
8. A Case of Reversible Infantile Respiratory Chain Deficiency Presenting With Hypotonia, Hyperammonemia, and Failure to Thrive. Guerrero JC; Pedro H; Parisotto S; Heller D; Baisre-de Leon A Pediatr Dev Pathol; 2019; 22(6):590-593. PubMed ID: 31333056 [TBL] [Abstract][Full Text] [Related]
10. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin. Boustany RN; Aprille JR; Halperin J; Levy H; DeLong GR Ann Neurol; 1983 Oct; 14(4):462-70. PubMed ID: 6314875 [TBL] [Abstract][Full Text] [Related]
11. Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency. Zeviani M; Van Dyke DH; Servidei S; Bauserman SC; Bonilla E; Beaumont ET; Sharda J; VanderLaan K; DiMauro S Arch Neurol; 1986 Nov; 43(11):1198-202. PubMed ID: 3022695 [TBL] [Abstract][Full Text] [Related]
12. Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient. Zeviani M; Nonaka I; Bonilla E; Okino E; Moggio M; Jones S; DiMauro S Ann Neurol; 1985 Apr; 17(4):414-7. PubMed ID: 2988412 [TBL] [Abstract][Full Text] [Related]
13. Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase. Roodhooft AM; Van Acker KJ; Martin JJ; Ceuterick C; Scholte HR; Luyt-Houwen IE Neuropediatrics; 1986 Nov; 17(4):221-6. PubMed ID: 3027606 [TBL] [Abstract][Full Text] [Related]
14. Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency. DiMauro S; Mendell JR; Sahenk Z; Bachman D; Scarpa A; Scofield RM; Reiner C Neurology; 1980 Aug; 30(8):795-804. PubMed ID: 6251406 [TBL] [Abstract][Full Text] [Related]
15. Benign reversible muscle cytochrome c oxidase deficiency: a second case. Zeviani M; Peterson P; Servidei S; Bonilla E; DiMauro S Neurology; 1987 Jan; 37(1):64-7. PubMed ID: 3025776 [TBL] [Abstract][Full Text] [Related]
16. 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 [TBL] [Abstract][Full Text] [Related]
17. [Mitochondrial encephalomyopathy (focal cytochrome c oxidase deficiency) with transient episodes of muscle weakness and elevation of serum creatine kinase activity]. Ohno M; Kobayashi T; Tanaka K; Goto I; Nonaka I Rinsho Shinkeigaku; 1990 Mar; 30(3):317-9. PubMed ID: 2163788 [TBL] [Abstract][Full Text] [Related]
18. 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; 30(1):56-60. PubMed ID: 2153548 [TBL] [Abstract][Full Text] [Related]
19. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report]. Oya Y; Segawa M; Ogawa M; Goto Y; Nonaka I; Kawai M Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727 [TBL] [Abstract][Full Text] [Related]