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Journal Abstract Search

454 related items for PubMed ID: 16224730

  • 1. [Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients].
    Arpa-Gutiérrez FJ, Cruz-Martínez A, Campos-González Y, Gutiérrez-Molina M, Santiago-Pérez S, Pérez-Conde MC, López-Pajares MR, Martín-Casarrubias MA, Rubio-Muñoz JC, del Hoyo P, Arpa-Fernández A, Arenas-Barbero J.
    Rev Neurol; ; 41(8):449-54. PubMed ID: 16224730
    [Abstract] [Full Text] [Related]

  • 2. [Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases].
    Arpa J, Campos Y, Cruz Martínez A, Gutiérrez Molina M, Arenas J, Alonso M, Plaza I, Morales C, Palomo F, Barreiro P.
    Neurologia; 1994 Oct; 9(8):324-36. PubMed ID: 7803049
    [Abstract] [Full Text] [Related]

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

  • 4. Apoptosis-related changes in skeletal muscles of patients with mitochondrial diseases.
    Umaki Y, Mitsui T, Endo I, Akaike M, Matsumoto T.
    Acta Neuropathol; 2002 Feb; 103(2):163-70. PubMed ID: 11810183
    [Abstract] [Full Text] [Related]

  • 5. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].
    Zhang Y, Wang ZX, Niu SL, Xu YF, Pei P, Yuan Y, Yang YL, Qi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb; 27(1):77-80. PubMed ID: 15782498
    [Abstract] [Full Text] [Related]

  • 6. Headache and mitochondrial disorders.
    Rosen N.
    Headache; 2008 May; 48(5):733-4. PubMed ID: 18471127
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial diseases.
    Nonaka I.
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
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  • 11. [Progressive external ophthalmoplegia and the Kearns-Sayre syndrome: a clinical and molecular study of 6 cases].
    Barrientos A, Casademont J, Grau JM, Cardellach F, Montoya J, Estivill X, Urbano-Márquez A, Nunes V.
    Med Clin (Barc); 1995 Jul 01; 105(5):180-4. PubMed ID: 7630231
    [Abstract] [Full Text] [Related]

  • 12. [Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies].
    Suzuki S.
    Nihon Rinsho; 1994 Oct 01; 52(10):2606-10. PubMed ID: 7527090
    [Abstract] [Full Text] [Related]

  • 13. Defects of mitochondrial DNA.
    Zeviani M, Antozzi C.
    Brain Pathol; 1992 Apr 01; 2(2):121-32. PubMed ID: 1341953
    [Abstract] [Full Text] [Related]

  • 14. Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers.
    Challa S, Kanikannan MA, Murthy JM, Bhoompally VR, Surath M.
    Neurol India; 2004 Sep 01; 52(3):353-8. PubMed ID: 15472426
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome.
    Sproule DM, Kaufmann P.
    Ann N Y Acad Sci; 2008 Oct 01; 1142():133-58. PubMed ID: 18990125
    [Abstract] [Full Text] [Related]

  • 16. [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].
    Mitsuoka T, Kawarai T, Watanabe C, Katayama S, Nakamura S.
    No To Shinkei; 1998 Dec 01; 50(12):1089-92. PubMed ID: 9989353
    [Abstract] [Full Text] [Related]

  • 17. The molecular genetics of mitochondrial cytopathies: the Melbourne experience.
    Thyagarajan D, Byrne E, Dennet X, Marzuki S.
    Clin Exp Neurol; 1992 Dec 01; 29():172-81. PubMed ID: 1343860
    [Abstract] [Full Text] [Related]

  • 18. Characteristic cardiac phenotypes are detected by cardiovascular magnetic resonance in patients with different clinical phenotypes and genotypes of mitochondrial myopathy.
    Florian A, Ludwig A, Stubbe-Dräger B, Boentert M, Young P, Waltenberger J, Rösch S, Sechtem U, Yilmaz A.
    J Cardiovasc Magn Reson; 2015 May 22; 17(1):40. PubMed ID: 26001801
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
    Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S.
    N Engl J Med; 1989 May 18; 320(20):1293-9. PubMed ID: 2541333
    [Abstract] [Full Text] [Related]

  • 20. 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]

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