BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

334 related articles for article (PubMed ID: 31345444)

  • 1. 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]  

  • 2. 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]  

  • 3. Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon).
    Niedermayr K; Pölzl G; Scholl-Bürgi S; Fauth C; Schweigmann U; Haberlandt E; Albrecht U; Zlamy M; Sperl W; Mayr JA; Karall D
    Congenit Heart Dis; 2018 Sep; 13(5):671-677. PubMed ID: 30133155
    [TBL] [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. Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation.
    Scarcella S; Dell'Arti L; Gagliardi D; Magri F; Govoni A; Velardo D; Mainetti C; Minorini V; Ronchi D; Piga D; Comi GP; Corti S; Meneri M
    BMC Neurol; 2023 Apr; 23(1):165. PubMed ID: 37095452
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].
    Liu XL; Bao XH; Ma YN; Chang XZ; Qin J; Wu XR
    Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):130-5. PubMed ID: 23527980
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the
    Endres D; Süß P; Maier SJ; Friedel E; Nickel K; Ziegler C; Fiebich BL; Glocker FX; Stock F; Egger K; Lange T; Dacko M; Venhoff N; Erny D; Doostkam S; Komlosi K; Domschke K; Tebartz van Elst L
    Front Immunol; 2019; 10():412. PubMed ID: 30949164
    [No Abstract]   [Full Text] [Related]  

  • 13. Treatment options for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
    Santa KM
    Pharmacotherapy; 2010 Nov; 30(11):1179-96. PubMed ID: 20973690
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population.
    Tatlisumak T; Putaala J; Innilä M; Enzinger C; Metso TM; Curtze S; von Sarnowski B; Amaral-Silva A; Jungehulsing GJ; Tanislav C; Thijs V; Rolfs A; Norrving B; Fazekas F; Suomalainen A; Kolodny EH
    J Neurol; 2016 Feb; 263(2):257-262. PubMed ID: 26566914
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.
    Wang YX; Le WD
    Chin Med J (Engl); 2015 Jul; 128(13):1820-5. PubMed ID: 26112726
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection.
    Marotta R; Reardon K; McKelvie PA; Chiotis M; Chin J; Cook M; Collins SJ
    J Clin Neurosci; 2009 Sep; 16(9):1223-5. PubMed ID: 19502062
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neuroimaging pattern and pathophysiology of cerebellar stroke-like lesions in MELAS with m.3243A>G mutation: a case report.
    Oyama M; Iizuka T; Nakahara J; Izawa Y
    BMC Neurol; 2020 May; 20(1):167. PubMed ID: 32357846
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.