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267 related items for PubMed ID: 8301880

  • 1. 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; 47(3):637-41. PubMed ID: 8301880
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Murakami T, Kumamoto T, Uchino M, Nonaka I, Ando M.
    Ann Neurol; 1994 Apr; 35(4):413-9. PubMed ID: 8154867
    [Abstract] [Full Text] [Related]

  • 4. 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; 56(1):95-99. PubMed ID: 28050007
    [Abstract] [Full Text] [Related]

  • 5. The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.
    Moraes CT, Ricci E, Bonilla E, DiMauro S, Schon EA.
    Am J Hum Genet; 1992 May; 50(5):934-49. PubMed ID: 1315123
    [Abstract] [Full Text] [Related]

  • 6. MELAS syndrome: correlation between clinical features and molecular genetic analysis.
    Liou CW, Huang CC, Chee EC, Jong YJ, Tsai JL, Pang CY, Lee HC, Wei YH.
    Acta Neurol Scand; 1994 Nov; 90(5):354-9. PubMed ID: 7887136
    [Abstract] [Full Text] [Related]

  • 7. 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; 13(1):69-72. PubMed ID: 7575854
    [Abstract] [Full Text] [Related]

  • 8. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S.
    Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
    [Abstract] [Full Text] [Related]

  • 9. Monozygotic twins with MELAS-like syndrome lacking ragged red fibers and lactacidaemia.
    Melberg A, Akerlund P, Raininko R, Silander HC, Wibom R, Khaled A, Nennesmo I, Lundberg PO, Olsson Y.
    Acta Neurol Scand; 1996 Oct; 94(4):233-41. PubMed ID: 8937533
    [Abstract] [Full Text] [Related]

  • 10. 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; 92(3):252-5. PubMed ID: 7484081
    [Abstract] [Full Text] [Related]

  • 11. 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; 34(3):235-8. PubMed ID: 16504796
    [Abstract] [Full Text] [Related]

  • 12. [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]

  • 13. Atypical MELAS associated with mitochondrial tRNA(Lys) gene A8296G mutation.
    Sakuta R, Honzawa S, Murakami N, Goto Y, Nagai T.
    Pediatr Neurol; 2002 Nov 18; 27(5):397-400. PubMed ID: 12504210
    [Abstract] [Full Text] [Related]

  • 14. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.
    Zeviani M, Muntoni F, Savarese N, Serra G, Tiranti V, Carrara F, Mariotti C, DiDonato S.
    Eur J Hum Genet; 1993 Nov 18; 1(1):80-7. PubMed ID: 8069654
    [Abstract] [Full Text] [Related]

  • 15. Heteroplasmic mitochondrial DNA mutation in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Chiang LM, Jong YJ, Huang SC, Tsai JL, Pang CY, Lee HC, Wei YH.
    J Formos Med Assoc; 1995 Nov 18; 94(1-2):42-7. PubMed ID: 7613232
    [Abstract] [Full Text] [Related]

  • 16. 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 18; 110(11):851-5. PubMed ID: 9772417
    [Abstract] [Full Text] [Related]

  • 17. A juvenile case of MELAS with T3271C mitochondrial DNA mutation.
    Stenqvist L, Paetau A, Valanne L, Suomalainen A, Pihko H.
    Pediatr Res; 2005 Aug 18; 58(2):258-62. PubMed ID: 16006433
    [Abstract] [Full Text] [Related]

  • 18. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: molecular genetic analysis and family study.
    Onishi H, Inoue K, Osaka H, Kimura S, Nagatomo H, Hanihara T, Kawamoto S, Okuda K, Yamada Y, Kosaka K.
    J Neurol Sci; 1993 Feb 18; 114(2):205-8. PubMed ID: 8445402
    [Abstract] [Full Text] [Related]

  • 19. [MELAS: Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes].
    Murakami H, Ono K.
    Brain Nerve; 2017 Feb 18; 69(2):111-117. PubMed ID: 28202819
    [Abstract] [Full Text] [Related]

  • 20. Mitochondrial respiratory-chain defects presenting as nonspecific features in children.
    Tsao CY, Mendell JR, Lo WD, Luquette M, Rusin J.
    J Child Neurol; 2000 Jul 18; 15(7):445-8. PubMed ID: 10921514
    [Abstract] [Full Text] [Related]

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