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Journal Abstract Search

157 related items for PubMed ID: 35266136

  • 21.
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  • 22. Diabetes ketoacidosis and Recurrent Childhood Stroke-like Episodes.
    Liu RC, Sheu JN, Liu CS, Tsai JD.
    Acta Neurol Taiwan; 2024 Mar 30; 33(1)():41-42. PubMed ID: 37853548
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  • 23. 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 30; 260(4):1071-80. PubMed ID: 23196335
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  • 24. Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome in pregnancy.
    Balachandran Nair D, Bloomfield M, Parasuraman R, Howe DT.
    BMJ Case Rep; 2021 Apr 07; 14(4):. PubMed ID: 33827862
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  • 25. MELAS without ragged red fibers or lactic acidosis diagnosed by mitochondrial DNA testing.
    Ujike H, Wakagi T, Kohira I, Kuroda S, Otsuki S, Sato T.
    Jpn J Psychiatry Neurol; 1993 Sep 07; 47(3):637-41. PubMed ID: 8301880
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  • 26. 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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  • 29. [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 21; 51(2):130-5. PubMed ID: 23527980
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  • 30. 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 12; 17(1):10. PubMed ID: 33438095
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  • 35. [G14453A mutation in mitochondrial myopathy encephalomyopathy with lactic acidosis and stroke-like episodes].
    Zheng X, Zhang Y, Zhang Y, Pei P, Ma Y.
    Zhonghua Yi Xue Za Zhi; 2015 Aug 25; 95(32):2623-5. PubMed ID: 26711613
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  • 37. Molecular and neurological features of MELAS syndrome in paediatric patients: A case series and review of the literature.
    Seed LM, Dean A, Krishnakumar D, Phyu P, Horvath R, Harijan PD.
    Mol Genet Genomic Med; 2022 Jul 25; 10(7):e1955. PubMed ID: 35474314
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  • 39. 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 06; 13(1):63. PubMed ID: 30837005
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  • 40. A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes.
    Campos Y, Lorenzo G, Martín MA, Torregrosa A, del Hoyo P, Rubio JC, García A, Arenas J.
    Neuromuscul Disord; 2000 Oct 06; 10(7):493-6. PubMed ID: 10996780
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