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9. [Mitochondrial myopathy and mitochondrial encephalomyopathy]. Song D; Liu C; Lu Q; Shi J; Chen J; Zhang H; Zhang Y; Wang H; Zhang W; Li G Zhonghua Yi Xue Za Zhi; 2002 Feb; 82(3):158-60. PubMed ID: 11953149 [TBL] [Abstract][Full Text] [Related]
10. [Ultrastructural and clinical findings of mitochondrial encephalomyopathy:report of 27 cases]. Zhang Q; Sun YL; Zhang CP; Qu BQ; Zhang ZQ Zhonghua Bing Li Xue Za Zhi; 2019 Apr; 48(4):298-302. PubMed ID: 30955266 [No Abstract] [Full Text] [Related]
11. [MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes]. Mierzewska H; Mroczek K; Pronicki M; Pronicka E; Karczmarewicz E; Bartnik E; Zdzienicka E; Seniów J; Schmidt-Sidor B; Taraszewska A; Palasik W Neurol Neurochir Pol; 2002; 36(3):457-70. PubMed ID: 12185802 [TBL] [Abstract][Full Text] [Related]
12. [Mitochondrial encephalomyopathies. A comparison of Kearns-Sayre syndrome, MELAS and MERRF]. Zenner K; Gold R; Meurers B; Reichmann H Nervenarzt; 1990 Oct; 61(10):597-603. PubMed ID: 2177152 [No Abstract] [Full Text] [Related]
13. Stimulation of oxygen consumption of platelets by Solcoseryl and cardiocrome during in vitro aging for 5 days. Shimizu T Jpn J Pharmacol; 1990 Aug; 53(4):499-501. PubMed ID: 2170724 [TBL] [Abstract][Full Text] [Related]
14. [Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients]. Arpa-Gutiérrez FJ; Cruz-Martínez A; Campos-González Y; Gutiérrez-Molina M; Santiago-Pérez S; Pérez-Conde MC; López-Pajares MR; Martín-Casarrubias MA; Rubio-Muñoz JC; del Hoyo P; Arpa-Fernández A; Arenas-Barbero J Rev Neurol; 2005 Oct 16-31; 41(8):449-54. PubMed ID: 16224730 [TBL] [Abstract][Full Text] [Related]
15. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes. Nakamura M; Yabe I; Sudo A; Hosoki K; Yaguchi H; Saitoh S; Sasaki H J Med Genet; 2010 Oct; 47(10):659-64. PubMed ID: 20610441 [TBL] [Abstract][Full Text] [Related]
16. Outbreak of life-threatening thiamine deficiency in infants in Israel caused by a defective soy-based formula. Fattal-Valevski A; Kesler A; Sela BA; Nitzan-Kaluski D; Rotstein M; Mesterman R; Toledano-Alhadef H; Stolovitch C; Hoffmann C; Globus O; Eshel G Pediatrics; 2005 Feb; 115(2):e233-8. PubMed ID: 15687431 [TBL] [Abstract][Full Text] [Related]
17. An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA. Terauchi A; Tamagawa K; Morimatsu Y; Kobayashi M; Sano T; Yoda S Brain Dev; 1996; 18(3):224-9. PubMed ID: 8836506 [TBL] [Abstract][Full Text] [Related]
18. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation]. Zhang Y; Wang ZX; Niu SL; Xu YF; Pei P; Yuan Y; Yang YL; Qi Y Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb; 27(1):77-80. PubMed ID: 15782498 [TBL] [Abstract][Full Text] [Related]
19. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies. Zwirner P; Wilichowski E Laryngoscope; 2001 Mar; 111(3):515-21. PubMed ID: 11224785 [TBL] [Abstract][Full Text] [Related]
20. Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies. Mathews PM; Andermann F; Silver K; Karpati G; Arnold DL Neurology; 1993 Dec; 43(12):2484-90. PubMed ID: 8255444 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]