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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
313 related items for PubMed ID: 2553313
1. [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 [Abstract] [Full Text] [Related]
2. MELAS syndrome: peripheral neuropathy and cytochrome C-oxidase deficiency: a case report and review of the literature. Barak Y, Arnon S, Wolach B, Raz Y, Ashkenasi A, Glick B, Shapira Y. Isr J Med Sci; 1995 Apr; 31(4):224-9. PubMed ID: 7721560 [Abstract] [Full Text] [Related]
4. [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 [Abstract] [Full Text] [Related]
5. [MELAS-like episodes in an adult case with cytochrome c oxidase deficiency]. Kihira T, Kohmoto J, Yoshida S, Hironishi M, Kondo T, Nakao N, Goto Y, Nishino K, Nonaka I. Rinsho Shinkeigaku; 2004 Mar; 44(3):187-92. PubMed ID: 15233272 [Abstract] [Full Text] [Related]
14. [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]
15. Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome. Kobayashi M, Morishita H, Sugiyama N, Yokochi K, Nakano M, Wada Y, Hotta Y, Terauchi A, Nonaka I. J Pediatr; 1987 Feb; 110(2):223-7. PubMed ID: 3100753 [Abstract] [Full Text] [Related]
19. Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Hasegawa H, Matsuoka T, Goto Y, Nonaka I. Ann Neurol; 1991 Jun; 29(6):601-5. PubMed ID: 1892363 [Abstract] [Full Text] [Related]
20. 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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]