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.
182 related articles for article (PubMed ID: 29471047)
1. A urinary biosignature for mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like episodes (MELAS). Esterhuizen K; Lindeque JZ; Mason S; van der Westhuizen FH; Suomalainen A; Hakonen AH; Carroll CJ; Rodenburg RJ; de Laat PB; Janssen MCH; Smeitink JAM; Louw R Mitochondrion; 2019 Mar; 45():38-45. PubMed ID: 29471047 [TBL] [Abstract][Full Text] [Related]
2. One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation. Esterhuizen K; Lindeque JZ; Mason S; van der Westhuizen FH; Rodenburg RJ; de Laat P; Smeitink JAM; Janssen MCH; Louw R Metabolomics; 2021 Jan; 17(1):10. PubMed ID: 33438095 [TBL] [Abstract][Full Text] [Related]
3. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome. Sproule DM; Kaufmann P Ann N Y Acad Sci; 2008 Oct; 1142():133-58. PubMed ID: 18990125 [TBL] [Abstract][Full Text] [Related]
4. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options. El-Hattab AW; Adesina AM; Jones J; Scaglia F Mol Genet Metab; 2015; 116(1-2):4-12. PubMed ID: 26095523 [TBL] [Abstract][Full Text] [Related]
5. A case of exacerbated encephalopathy with stroke-like episodes and lactic acidosis triggered by metformin in a patient with MELAS. Shin HJ; Na JH; Lee YM Neurol Sci; 2024 May; 45(5):2337-2339. PubMed ID: 38265537 [TBL] [Abstract][Full Text] [Related]
6. An autopsy case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with intestinal bleeding in chronic renal failure. Mima A; Shiota F; Matsubara T; Iehara N; Akagi T; Abe H; Nagai K; Matsuura M; Murakami T; Kishi S; Araoka T; Kishi F; Kondo N; Shigeta R; Yoshikawa K; Kita T; Doi T; Fukatsu A Ren Fail; 2011; 33(6):622-5. PubMed ID: 21631236 [TBL] [Abstract][Full Text] [Related]
7. The Usefulness of Muscle Biopsy in Initial Diagnostic Evaluation of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes. Baek MS; Kim SH; Lee YM Yonsei Med J; 2019 Jan; 60(1):98-105. PubMed ID: 30554496 [TBL] [Abstract][Full Text] [Related]
8. Independent origin for m.3243A>G mitochondrial mutation in three Venezuelan cases of MELAS syndrome. Florez I; Pirrone I; Casique L; Domínguez CL; Mahfoud A; Rodríguez T; Rodríguez D; De Lucca M; Ramírez JL Clin Biochem; 2022; 109-110():98-101. PubMed ID: 36130631 [TBL] [Abstract][Full Text] [Related]
9. Late-onset mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with bitemporal lesions. Kisanuki YY; Gruis KL; Smith TL; Brown DL Arch Neurol; 2006 Aug; 63(8):1200-1. PubMed ID: 16908753 [No Abstract] [Full Text] [Related]
10. Gastro-intestinal Involvement in m.3243A>G-associated Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes. Suzuki J; Iwata M; Moriyoshi H; Nishida S; Yasuda T; Ito Y Intern Med; 2018 Mar; 57(5):771. PubMed ID: 29151541 [No Abstract] [Full Text] [Related]
11. Focal cerebellar infarction as an initial sign of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Ko A; Lee SJ; Lee YM J Inherit Metab Dis; 2019 May; 42(3):575-576. PubMed ID: 30693531 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes due to m.3243A > G mutation in a 76-year-old woman. Ueki K; Wakisaka Y; Nakamura K; Shono Y; Wada S; Yoshikawa Y; Matsukuma Y; Uchiumi T; Kang D; Kitazono T; Ago T J Neurol Sci; 2020 May; 412():116791. PubMed ID: 32224343 [No Abstract] [Full Text] [Related]
13. The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options. Scaglia F; Northrop JL CNS Drugs; 2006; 20(6):443-64. PubMed ID: 16734497 [TBL] [Abstract][Full Text] [Related]
14. Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis. Monnot S; Samuels DC; Hesters L; Frydman N; Gigarel N; Burlet P; Kerbrat V; Lamazou F; Frydman R; Benachi A; Feingold J; Rotig A; Munnich A; Bonnefont JP; Steffann J Hum Mol Genet; 2013 May; 22(9):1867-72. PubMed ID: 23390135 [TBL] [Abstract][Full Text] [Related]
15. Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes. Mukai M; Nagata E; Mizuma A; Yamano M; Sugaya K; Nishino I; Goto YI; Takizawa S Intern Med; 2017; 56(1):95-99. PubMed ID: 28050007 [TBL] [Abstract][Full Text] [Related]
17. A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome. Li JY; Hsieh RH; Peng NJ; Lai PH; Lee CF; Lo YK; Wei YH J Formos Med Assoc; 2007 Jul; 106(7):528-36. PubMed ID: 17660142 [TBL] [Abstract][Full Text] [Related]
18. Data-independent acquisition-based quantitative proteomic analysis of m.3243A>G MELAS reveals novel potential pathogenesis and therapeutic targets. Chang X; Yin Z; Zhang W; Shi J; Pu C; Shi Q; Wang J; Zhang J; Yan L; Yang W; Guo J Medicine (Baltimore); 2022 Oct; 101(41):e30938. PubMed ID: 36254078 [TBL] [Abstract][Full Text] [Related]
19. Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy. Mukai M; Nagata E Intern Med; 2017 Oct; 56(19):2695. PubMed ID: 28883258 [No Abstract] [Full Text] [Related]
20. Molecular imaging for mitochondrial metabolism and oxidative stress in mitochondrial diseases and neurodegenerative disorders. Ikawa M; Okazawa H; Yoneda M Biochim Biophys Acta Gen Subj; 2021 Mar; 1865(3):129832. PubMed ID: 33358866 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]