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272 related items for PubMed ID: 27453332

  • 1. Acute encephalopathy of the temporal lobes leading to m.3243A>G. When MELAS is not always MELAS.
    Caldarazzo Ienco E, Orsucci D, Simoncini C, Montano V, LoGerfo A, Siciliano G, Bonuccelli U, Mancuso M.
    Mitochondrion; 2016 Sep; 30():148-50. PubMed ID: 27453332
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  • 2. [MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].
    de Toledo M, Díaz-Guzmán J, Pérez-Martínez DA, Sáiz-Díaz RA, Rodríguez-Vallejo A, Campos Y.
    Rev Neurol; 2016 Sep; 33(2):148-50. PubMed ID: 11562875
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  • 3. Adult-onset of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome presenting as acute meningoencephalitis: a case report.
    Hsu YC, Yang FC, Perng CL, Tso AC, Wong LJ, Hsu CH.
    J Emerg Med; 2012 Sep; 43(3):e163-6. PubMed ID: 20036095
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  • 4. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome mimicking herpes simplex encephalitis on imaging studies.
    Gieraerts C, Demaerel P, Van Damme P, Wilms G.
    J Comput Assist Tomogr; 2013 Sep; 37(2):279-81. PubMed ID: 23493219
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  • 5. 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 01; 20(1):167. PubMed ID: 32357846
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  • 6. 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 01; 13(5):671-677. PubMed ID: 30133155
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  • 7. Can diffusion weighted magnetic resonance imaging help differentiate stroke from stroke-like events in MELAS?
    Oppenheim C, Galanaud D, Samson Y, Sahel M, Dormont D, Wechsler B, Marsault C.
    J Neurol Neurosurg Psychiatry; 2000 Aug 01; 69(2):248-50. PubMed ID: 10896703
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  • 8. Intravoxel incoherent motion magnetic resonance imaging findings in the acute phase of MELAS: a case report.
    Uehara R, Yamashita K, Hiwatashi A, Togao O, Kikuchi K, Yokoyama J, Matsuse D, Yoshiura T, Honda H.
    Brain Behav; 2014 Aug 01; 4(6):798-800. PubMed ID: 25365795
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  • 12. The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.
    Leng Y, Liu Y, Fang X, Li Y, Yu L, Yuan Y, Wang Z.
    Mitochondrial DNA; 2015 Apr 01; 26(2):208-12. PubMed ID: 24708134
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  • 14. 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 01; 41(10):901-904. PubMed ID: 31345444
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  • 16. Adult-onset MELAS presenting as herpes encephalitis.
    Sharfstein SR, Gordon MF, Libman RB, Malkin ES.
    Arch Neurol; 1999 Feb 01; 56(2):241-3. PubMed ID: 10025431
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  • 20. 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 Feb 01; 109-110():98-101. PubMed ID: 36130631
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