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Journal Abstract Search

201 related items for PubMed ID: 33300189

  • 1. Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes/Leigh syndrome overlap patient with a novel m.3482A>G mutation in MT-ND1.
    Hayashi Y, Iwasaki Y, Yoshikura N, Yamada M, Kimura A, Inuzuka T, Miyahara H, Goto Y, Nishino I, Yoshida M, Shimohata T.
    Neuropathology; 2021 Feb; 41(1):84-90. PubMed ID: 33300189
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  • 2. [Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes / myoclonus epilepsy with ragged-red fibers /Leigh overlap syndrome caused by mitochondrial DNA 8344A>G mutation].
    Hou Y, Zhao XT, Xie ZY, Yuan Y, Wang ZX.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct 18; 52(5):851-855. PubMed ID: 33047718
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  • 3. Phenotypic patterns of MELAS/LS overlap syndrome associated with m.13513G>A mutation, and neuropathological findings in one autopsy case.
    Wang Z, Qi XK, Yao S, Chen B, Luan X, Zhang W, Han M, Yuan Y.
    Neuropathology; 2010 Dec 18; 30(6):606-14. PubMed ID: 20408961
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  • 4. 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 18; 26(2):208-12. PubMed ID: 24708134
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  • 5. An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA.
    Terauchi A, Tamagawa K, Morimatsu Y, Kobayashi M, Sano T, Yoda S.
    Brain Dev; 1996 Apr 18; 18(3):224-9. PubMed ID: 8836506
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  • 12. 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 18; 24(7):828-32. PubMed ID: 19617458
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  • 13. 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 18; 32(5):107080. PubMed ID: 36933522
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  • 16. 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 May 18; 10():412. PubMed ID: 30949164
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  • 17. 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 18; 41(9):803-807. PubMed ID: 31178082
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  • 18. The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypes.
    Vacchiano V, Caporali L, La Morgia C, Carbonelli M, Amore G, Bartolomei I, Cascavilla ML, Barboni P, Lamperti C, Catania A, Chan JW, Karanja R, Sadun AA, Liguori R, Bianchi A, Gavazzi G, Mascalchi M, Salvi F, Carelli V.
    Mitochondrion; 2021 Sep 18; 60():142-149. PubMed ID: 34390870
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