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Journal Abstract Search

356 related items for PubMed ID: 11553931

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

  • 2. Mitochondrial cytopathies.
    Schmiedel J, Jackson S, Schäfer J, Reichmann H.
    J Neurol; 2003 Mar; 250(3):267-77. PubMed ID: 12638015
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial disorders in muscle.
    Schon EA.
    Curr Opin Neurol Neurosurg; 1993 Feb; 6(1):19-26. PubMed ID: 8428062
    [Abstract] [Full Text] [Related]

  • 4. Mouse models for mitochondrial disease.
    Wallace DC.
    Am J Med Genet; 2001 Feb; 106(1):71-93. PubMed ID: 11579427
    [Abstract] [Full Text] [Related]

  • 5. The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement.
    Wallace DC.
    Gene; 2005 Jul 18; 354():169-80. PubMed ID: 16024186
    [Abstract] [Full Text] [Related]

  • 6. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
    Liu CS, Cheng WL, Lee CF, Ma YS, Lin CY, Huang CC, Wei YH.
    Acta Neurol Scand; 2006 May 18; 113(5):334-41. PubMed ID: 16629770
    [Abstract] [Full Text] [Related]

  • 7. Animal models for mitochondrial disease.
    Wallace DC.
    Methods Mol Biol; 2002 May 18; 197():3-54. PubMed ID: 12013805
    [Abstract] [Full Text] [Related]

  • 8. [Mitochondrial DNA mutations and three major forms of mitochondrial myopathies: CPEO, MELAS and MERRF].
    Goto Y.
    Nihon Rinsho; 1997 Dec 18; 55(12):3259-64. PubMed ID: 9436447
    [Abstract] [Full Text] [Related]

  • 9. Mitochondrial diseases.
    DiMauro S.
    Biochim Biophys Acta; 2004 Jul 23; 1658(1-2):80-8. PubMed ID: 15282178
    [Abstract] [Full Text] [Related]

  • 10. The genetics of mitochondrial disease.
    Davis RL, Sue CM.
    Semin Neurol; 2011 Nov 23; 31(5):519-30. PubMed ID: 22266889
    [Abstract] [Full Text] [Related]

  • 11. Update in molecular genetics: mitochondrial energy transduction disorders.
    Marzuki S, Sudoyo H, Lertrit P.
    Southeast Asian J Trop Med Public Health; 1995 Nov 23; 26 Suppl 1():155-61. PubMed ID: 8629096
    [No Abstract] [Full Text] [Related]

  • 12. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
    Du W, Li W, Chen G, Cao H, Tang H, Tang X, Jin Q, Sun Z, Zhao H, Zhou W, He S, Lv Y, Zhao J, Zhang X.
    Biosens Bioelectron; 2009 Apr 15; 24(8):2371-6. PubMed ID: 19155171
    [Abstract] [Full Text] [Related]

  • 13. [Mitochondrial genome and human mitochondrial diseases].
    Mazunin IO, Volod'ko NV, Starikovskaia EB, Sukernik RI.
    Mol Biol (Mosk); 2010 Apr 15; 44(5):755-72. PubMed ID: 21090233
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects.
    DiMauro S, Tanji K, Bonilla E, Pallotti F, Schon EA.
    Muscle Nerve; 2002 Nov 15; 26(5):597-607. PubMed ID: 12402281
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial DNA-related disorders.
    Mancuso M, Filosto M, Choub A, Tentorio M, Broglio L, Padovani A, Siciliano G.
    Biosci Rep; 2007 Jun 15; 27(1-3):31-7. PubMed ID: 17484046
    [Abstract] [Full Text] [Related]

  • 16. Clinical features of A3243G mitochondrial tRNA mutation.
    Chae JH, Hwang H, Lim BC, Cheong HI, Hwang YS, Kim KJ.
    Brain Dev; 2004 Oct 15; 26(7):459-62. PubMed ID: 15351082
    [Abstract] [Full Text] [Related]

  • 17. Rapid and noninvasive screening of patients with mitochondrial myopathy.
    Kotsimbos N, Jean-Francois MJ, Huizing M, Kapsa RM, Lertrit P, Siregar NC, Marzuki S, Sue C, Byrne E.
    Hum Mutat; 1994 Oct 15; 4(2):132-5. PubMed ID: 7981717
    [Abstract] [Full Text] [Related]

  • 18. MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.
    Mongini T, Doriguzzi C, Chiadò-Piat L, Silvestri G, Servidei S, Palmucci L.
    Clin Neuropathol; 2002 Oct 15; 21(2):72-6. PubMed ID: 12005255
    [Abstract] [Full Text] [Related]

  • 19. Diagnostic challenges of mitochondrial DNA disorders.
    Wong LJ.
    Mitochondrion; 2007 Oct 15; 7(1-2):45-52. PubMed ID: 17276740
    [Abstract] [Full Text] [Related]

  • 20. Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.
    Kolesnikova OA, Entelis NS, Jacquin-Becker C, Goltzene F, Chrzanowska-Lightowlers ZM, Lightowlers RN, Martin RP, Tarassov I.
    Hum Mol Genet; 2004 Oct 15; 13(20):2519-34. PubMed ID: 15317755
    [Abstract] [Full Text] [Related]

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