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Journal Abstract Search

214 related items for PubMed ID: 31807297

  • 1. 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
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  • 3. Impediments to Heart Transplantation in Adults With MELASMT-TL1:m.3243A>G Cardiomyopathy.
    Di Toro A, Urtis M, Narula N, Giuliani L, Grasso M, Pasotti M, Pellegrini C, Serio A, Pilotto A, Antoniazzi E, Rampino T, Magrassi L, Valentini A, Cavallini A, Scelsi L, Ghio S, Abelli M, Olivotto I, Porcu M, Gavazzi A, Kodama T, Arbustini E.
    J Am Coll Cardiol; 2022 Oct 11; 80(15):1431-1443. PubMed ID: 36202533
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  • 4. Renal manifestations in adults with mitochondrial disease from the mtDNA m.3243A>G pathogenic variant.
    Ferreira F, Gonçalves Bacelar C, Lisboa-Gonçalves P, Paulo N, Quental R, Nunes AT, Silva R, Tavares I.
    Nefrologia (Engl Ed); 2023 Dec 11; 43 Suppl 2():1-7. PubMed ID: 38355238
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  • 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 21; 13(1):313. PubMed ID: 31630688
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  • 8. MELAS Syndrome and Kidney Disease Without Fanconi Syndrome or Proteinuria: A Case Report.
    Rudnicki M, Mayr JA, Zschocke J, Antretter H, Regele H, Feichtinger RG, Windpessl M, Mayer G, Pölzl G.
    Am J Kidney Dis; 2016 Dec 21; 68(6):949-953. PubMed ID: 27683045
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  • 11. Reversal of Stroke-Like Episodes With L-Arginine and Meticulous Perioperative Management of Renal Transplantation in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome. Case Report.
    Al Yazidi G, Mulder J, Licht C, Harvey E, Robertson J, Sondheimer N, Tein I.
    Neurohospitalist; 2022 Jan 21; 12(1):67-73. PubMed ID: 34950389
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  • 12. Anatomic & metabolic brain markers of the m.3243A>G mutation: A multi-parametric 7T MRI study.
    Haast RAM, Ivanov D, IJsselstein RJT, Sallevelt SCEH, Jansen JFA, Smeets HJM, de Coo IFM, Formisano E, Uludağ K.
    Neuroimage Clin; 2018 Jan 21; 18():231-244. PubMed ID: 29868447
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  • 14. Focal segmental glomerulosclerosis associated with mitochondrial disease.
    Lim K, Steele D, Fenves A, Thadhani R, Heher E, Karaa A.
    Clin Nephrol Case Stud; 2017 Jan 21; 5():20-25. PubMed ID: 29043143
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  • 16. Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia.
    Liao NY, Lai KL, Liao YC, Hsiao CT, Lee YC.
    J Formos Med Assoc; 2023 Oct 21; 122(10):1028-1034. PubMed ID: 37311680
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  • 20. Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation.
    Tschampa HJ, Urbach H, Greschus S, Kunz WS, Kornblum C.
    J Neurol; 2013 Apr 21; 260(4):1071-80. PubMed ID: 23196335
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