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.
135 related articles for article (PubMed ID: 32466984)
1. Response to Letter regarding case report, "Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes due to m.3243A > G mutation in a 76-year-old woman". Ago T; Ueki K; Wakisaka Y; Nakamura K; Kitazono T J Neurol Sci; 2020 Jul; 414():116925. PubMed ID: 32466984 [No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report. Fukuda M; Nagao Y J Med Case Rep; 2019 Oct; 13(1):313. PubMed ID: 31630688 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Fulminant cerebral venous thrombosis associated with the m.3243A>G MELAS mutation: A new guise for an old disease. Nikolaus M; Tietze A; Schweizer L; Kaindl AM; Stenzel W; Schuelke M; Knierim E Brain Dev; 2019 Nov; 41(10):901-904. PubMed ID: 31345444 [TBL] [Abstract][Full Text] [Related]
8. Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy. Finsterer J; Zarrouk-Mahjoub S Intern Med; 2017 Oct; 56(19):2693. PubMed ID: 28883250 [No Abstract] [Full Text] [Related]
9. 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]
10. [A case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) complicated by chronic intestinal pseudo-obstruction]. Miyanaga R; Tanaka M; Nonaka T; Shizukawa H; Shimohama S Rinsho Shinkeigaku; 2022 Jun; 62(6):464-468. PubMed ID: 35644578 [TBL] [Abstract][Full Text] [Related]
11. A case of rhabdomyolysis after status epilepticus without stroke-like episodes in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Yokoyama J; Yamaguchi H; Shigeto H; Uchiumi T; Murai H; Kira JI Rinsho Shinkeigaku; 2017 Jul; 57(7):400-401. PubMed ID: 28637934 [No Abstract] [Full Text] [Related]
12. Chorea-ballism as a dominant clinical manifestation in heteroplasmic mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome with A3251G mutation in mitochondrial genome: a case report. Lahiri D; Sawale VM; Banerjee S; Dubey S; Roy BK; Das SK J Med Case Rep; 2019 Mar; 13(1):63. PubMed ID: 30837005 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. The phenotypic spectrum of fifty Czech m.3243A>G carriers. Dvorakova V; Kolarova H; Magner M; Tesarova M; Hansikova H; Zeman J; Honzik T Mol Genet Metab; 2016 Aug; 118(4):288-95. PubMed ID: 27296531 [TBL] [Abstract][Full Text] [Related]
16. [A case of rhabdomyolysis after status epilepticus without stroke-like episodes in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes]. Yokoyama J; Yamaguchi H; Shigeto H; Uchiumi T; Murai H; Kira J Rinsho Shinkeigaku; 2016; 56(3):204-7. PubMed ID: 26960270 [TBL] [Abstract][Full Text] [Related]
17. Five non-mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes phenotype adult patients with m.3243A>G mutation after kidney transplantation: follow-up and review of the literature. de Laat P; van Engelen N; Wetzels JF; Smeitink JAM; Janssen MCH Clin Kidney J; 2019 Dec; 12(6):840-846. PubMed ID: 31807297 [TBL] [Abstract][Full Text] [Related]