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Journal Abstract Search

234 related items for PubMed ID: 32541454

  • 21. New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2.
    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
    [Abstract] [Full Text] [Related]

  • 22. Diffuse posterior leukoencephalopathy in MELAS without stroke-like episodes: A case report.
    Bai P, Feng Y, Chen J, Chang H.
    Medicine (Baltimore); 2023 May 05; 102(18):e33725. PubMed ID: 37144988
    [Abstract] [Full Text] [Related]

  • 23. MERRF/MELAS overlap syndrome due to the m.3291T>C mutation.
    Liu K, Zhao H, Ji K, Yan C.
    Metab Brain Dis; 2014 Mar 05; 29(1):139-44. PubMed ID: 24338029
    [Abstract] [Full Text] [Related]

  • 24. An analysis of the clinical and imaging features of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Chen H, Hu Q, Raza HK, Chansysouphanthong T, Singh S, Rai P, Cui G, Zhang Z, Ye X, Xu C, Liu Y, Jiang H.
    Somatosens Mot Res; 2020 Mar 05; 37(1):45-49. PubMed ID: 32000557
    [Abstract] [Full Text] [Related]

  • 25. An autopsy case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with chronic renal failure.
    Yanagihara C, Oyama A, Tanaka M, Nakaji K, Nishimura Y.
    Intern Med; 2001 Jul 05; 40(7):662-5. PubMed ID: 11506313
    [Abstract] [Full Text] [Related]

  • 26. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.
    Pediatr Neurol; 2006 Mar 05; 34(3):235-8. PubMed ID: 16504796
    [Abstract] [Full Text] [Related]

  • 27. Mitochondrial encephalomyopathy lactic acidosis and strokelike episodes mimicking occipital idiopathic epilepsy.
    Cesaroni E, Scarpelli M, Zamponi N, Polonara G, Zeviani M.
    Pediatr Neurol; 2009 Aug 05; 41(2):131-4. PubMed ID: 19589463
    [Abstract] [Full Text] [Related]

  • 28. Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report.
    Alenezi AF, Almelahi MA, Fekih-Romdhana F, Jahrami HA.
    J Med Case Rep; 2022 Oct 10; 16(1):361. PubMed ID: 36210452
    [Abstract] [Full Text] [Related]

  • 29. Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
    Naini AB, Lu J, Kaufmann P, Bernstein RA, Mancuso M, Bonilla E, Hirano M, DiMauro S.
    Arch Neurol; 2005 Mar 10; 62(3):473-6. PubMed ID: 15767514
    [Abstract] [Full Text] [Related]

  • 30. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
    El-Hattab AW, Adesina AM, Jones J, Scaglia F.
    Mol Genet Metab; 2015 Mar 10; 116(1-2):4-12. PubMed ID: 26095523
    [Abstract] [Full Text] [Related]

  • 31. Transition from Leigh syndrome to MELAS syndrome in a patient with heteroplasmic MT-ND3 m.10158T>C.
    Kori A, Hori I, Tanaka T, Aoyama K, Ito K, Hattori A, Ban K, Okazaki Y, Murayama K, Saitoh S.
    Brain Dev; 2019 Oct 10; 41(9):803-807. PubMed ID: 31178082
    [Abstract] [Full Text] [Related]

  • 32. Atypical MELAS associated with mitochondrial tRNA(Lys) gene A8296G mutation.
    Sakuta R, Honzawa S, Murakami N, Goto Y, Nagai T.
    Pediatr Neurol; 2002 Nov 10; 27(5):397-400. PubMed ID: 12504210
    [Abstract] [Full Text] [Related]

  • 33. Mutations in ND subunits of complex I are an important genetic cause of childhood mitochondrial encephalopathies.
    Lim BC, Park JD, Hwang H, Kim KJ, Hwang YS, Chae JH, Cheon JE, Kim IO, Lee R, Moon HK.
    J Child Neurol; 2009 Jul 10; 24(7):828-32. PubMed ID: 19617458
    [Abstract] [Full Text] [Related]

  • 34. Prolonged misdiagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: A case report.
    Wang Y, Zhang W, Jiang X.
    Medicine (Baltimore); 2023 Nov 24; 102(47):e36008. PubMed ID: 38013338
    [Abstract] [Full Text] [Related]

  • 35. [Ultrastructural and clinical findings of mitochondrial encephalomyopathy:report of 27 cases].
    Zhang Q, Sun YL, Zhang CP, Qu BQ, Zhang ZQ.
    Zhonghua Bing Li Xue Za Zhi; 2019 Apr 08; 48(4):298-302. PubMed ID: 30955266
    [Abstract] [Full Text] [Related]

  • 36. 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 Apr 08; 56(1):95-99. PubMed ID: 28050007
    [Abstract] [Full Text] [Related]

  • 37. Leber hereditary optic neuropathy and dystonia overlapping mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes due to m.14459G>A mutation.
    Yu X, Ji K, Lin Y, Xu X, Wang W, Li Y, Lu JQ, Zhao Y, Yan C.
    Neurol Sci; 2021 Dec 08; 42(12):5123-5130. PubMed ID: 33779865
    [Abstract] [Full Text] [Related]

  • 38. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y, Guo Z, Chen L, Zhang J, Wang W, Liu X, Ren H, Gao S.
    Chin Med J (Engl); 1997 Nov 08; 110(11):851-5. PubMed ID: 9772417
    [Abstract] [Full Text] [Related]

  • 39. Disruption of endothelial tight junctions in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
    Matsuzaki M, Takahashi R, Nakayama T, Shishikura K, Suzuki H, Hirayama Y, Osawa M, Oda H.
    Neuropediatrics; 2010 Aug 08; 41(2):72-4. PubMed ID: 20799154
    [Abstract] [Full Text] [Related]

  • 40. Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes diagnosed after metformin-triggered stroke-like episodes.
    Murakami K, Sakamoto K, Ishiguchi H, Ito H.
    J Stroke Cerebrovasc Dis; 2023 May 08; 32(5):107080. PubMed ID: 36933522
    [Abstract] [Full Text] [Related]

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