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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 29151541)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. [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]  

  • 6. Familial Pernicious Chronic Intestinal Pseudo-obstruction with a Mitochondrial DNA A3243G Mutation.
    Suzuki J; Iwata M; Moriyoshi H; Nishida S; Yasuda T; Ito Y
    Intern Med; 2017; 56(9):1089-1093. PubMed ID: 28458318
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy.
    Chiyonobu T; Noda R; Yoshida M; Fujiki A; Ishii R; Nukina S; Fujita K; Goto Y; Morimoto M
    Brain Dev; 2008 Jun; 30(6):430-3. PubMed ID: 18226864
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Intestinal pseudo-obstruction and urinary retention: cardinal features of a mitochondrial DNA-related disease.
    García-Velasco A; Gómez-Escalonilla C; Guerra-Vales JM; Cabello A; Campos Y; Arenas J
    J Intern Med; 2003 Mar; 253(3):381-5. PubMed ID: 12603507
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
    Chakrabarty S; Govindaraj P; Sankaran BP; Nagappa M; Kabekkodu SP; Jayaram P; Mallya S; Deepha S; Ponmalar JNJ; Arivinda HR; Meena AK; Jha RK; Sinha S; Gayathri N; Taly AB; Thangaraj K; Satyamoorthy K
    J Neurol; 2021 Jun; 268(6):2192-2207. PubMed ID: 33484326
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial stroke-like episodes: The search for new therapies.
    Orsucci D; Caldarazzo Ienco E; Montano V; Siciliano G; Mancuso M
    Pharmacol Res; 2022 Jun; 180():106228. PubMed ID: 35462010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.