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Journal Abstract Search

234 related items for PubMed ID: 32541454

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. 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; 18(3):224-9. PubMed ID: 8836506
    [Abstract] [Full Text] [Related]

  • 3. [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; 51(2):130-5. PubMed ID: 23527980
    [Abstract] [Full Text] [Related]

  • 4. MELAS and macroangiopathy: A case report and literature review.
    Sun X, Jiang G, Ju X, Fu H.
    Medicine (Baltimore); 2018 Dec; 97(52):e13866. PubMed ID: 30593190
    [Abstract] [Full Text] [Related]

  • 5. Autopsied case with MERRF/MELAS overlap syndrome accompanied by stroke-like episodes localized to the precentral gyrus.
    Miyahara H, Matsumoto S, Mokuno K, Dei R, Akagi A, Mimuro M, Iwasaki Y, Yoshida M.
    Neuropathology; 2019 Jun; 39(3):212-217. PubMed ID: 30972844
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation.
    Scarcella S, Dell'Arti L, Gagliardi D, Magri F, Govoni A, Velardo D, Mainetti C, Minorini V, Ronchi D, Piga D, Comi GP, Corti S, Meneri M.
    BMC Neurol; 2023 Apr 24; 23(1):165. PubMed ID: 37095452
    [Abstract] [Full Text] [Related]

  • 8. CPEO and carnitine deficiency overlapping in MELAS syndrome.
    Hsu CC, Chuang YH, Tsai JL, Jong HJ, Shen YY, Huang HL, Chen HL, Lee HC, Pang CY, Wei YH.
    Acta Neurol Scand; 1995 Sep 24; 92(3):252-5. PubMed ID: 7484081
    [Abstract] [Full Text] [Related]

  • 9. Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy.
    Finsterer J, Zarrouk-Mahjoub S.
    Intern Med; 2017 Oct 01; 56(19):2693. PubMed ID: 28883250
    [No Abstract] [Full Text] [Related]

  • 10. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.
    Melone MA, Tessa A, Petrini S, Lus G, Sampaolo S, di Fede G, Santorelli FM, Cotrufo R.
    Arch Neurol; 2004 Feb 01; 61(2):269-72. PubMed ID: 14967777
    [Abstract] [Full Text] [Related]

  • 11. Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy.
    Mukai M, Nagata E.
    Intern Med; 2017 Oct 01; 56(19):2695. PubMed ID: 28883258
    [No Abstract] [Full Text] [Related]

  • 12. 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 01; 41(1):84-90. PubMed ID: 33300189
    [Abstract] [Full Text] [Related]

  • 13. [l-arginine efficiency in MELAS syndrome. A case report].
    Moutaouakil F, El Otmani H, Fadel H, Sefrioui F, Slassi I.
    Rev Neurol (Paris); 2009 May 01; 165(5):482-5. PubMed ID: 18849057
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.
    Campos Y, Garcia-Silva T, Barrionuevo CR, Cabello A, Muley R, Arenas J.
    Pediatr Neurol; 1995 Jul 01; 13(1):69-72. PubMed ID: 7575854
    [Abstract] [Full Text] [Related]

  • 15. [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
    [Abstract] [Full Text] [Related]

  • 16. A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome.
    Emmanuele V, Sotiriou E, Rios PG, Ganesh J, Ichord R, Foley AR, Akman HO, Dimauro S.
    J Child Neurol; 2013 Feb 18; 28(2):236-42. PubMed ID: 22638077
    [Abstract] [Full Text] [Related]

  • 17. 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 18; 10(7):493-6. PubMed ID: 10996780
    [Abstract] [Full Text] [Related]

  • 18. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M, Yabe I, Sudo A, Hosoki K, Yaguchi H, Saitoh S, Sasaki H.
    J Med Genet; 2010 Oct 18; 47(10):659-64. PubMed ID: 20610441
    [Abstract] [Full Text] [Related]

  • 19. 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 18; 47(3):637-41. PubMed ID: 8301880
    [Abstract] [Full Text] [Related]

  • 20. A novel tRNA(Val) mitochondrial DNA mutation causing MELAS.
    Tanji K, Kaufmann P, Naini AB, Lu J, Parsons TC, Wang D, Willey JZ, Shanske S, Hirano M, Bonilla E, Khandji A, Dimauro S, Rowland LP.
    J Neurol Sci; 2008 Jul 15; 270(1-2):23-7. PubMed ID: 18314141
    [Abstract] [Full Text] [Related]

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