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Journal Abstract Search

504 related items for PubMed ID: 12638015

  • 1. 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]

  • 2. The genetics of mitochondrial disease.
    Davis RL, Sue CM.
    Semin Neurol; 2011 Nov; 31(5):519-30. PubMed ID: 22266889
    [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. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy].
    Ito T.
    Nihon Rinsho; 1993 Jun; 51(6):1425-8. PubMed ID: 8320824
    [Abstract] [Full Text] [Related]

  • 5. Maternal inheritance and the evaluation of oxidative phosphorylation diseases.
    Shoffner JM.
    Lancet; 1996 Nov 09; 348(9037):1283-8. PubMed ID: 8909383
    [Abstract] [Full Text] [Related]

  • 6. Mitochondrial encephalomyopathies.
    Eymard B, Hauw JJ.
    Curr Opin Neurol Neurosurg; 1992 Dec 09; 5(6):909-16. PubMed ID: 1467585
    [Abstract] [Full Text] [Related]

  • 7. [Mutations in mitochondrial DNA in ocular diseases--Leher's hereditary optic neuropathy and Kearns' syndrome].
    Rydzanicz M, Mrugacz M, Gajecka M.
    Klin Oczna; 2008 Dec 09; 110(7-9):321-4. PubMed ID: 19112871
    [Abstract] [Full Text] [Related]

  • 8. Neurological mitochondrial cytopathies.
    Mehndiratta MM, Agarwal P, Tatke M, Krishnamurthy M.
    Neurol India; 2002 Jun 09; 50(2):162-7. PubMed ID: 12134180
    [Abstract] [Full Text] [Related]

  • 9. Genotype-phenotype correlation of maternally inherited disorders due to mutations in mitochondrial DNA.
    Thajeb P, Dai D, Chiang MF, Shyu WC.
    Taiwan J Obstet Gynecol; 2006 Sep 09; 45(3):201-7. PubMed ID: 17175464
    [Abstract] [Full Text] [Related]

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  • 11. Mitochondrial mutations in neuro-ophthalmological diseases. A review.
    Morris MA.
    J Clin Neuroophthalmol; 1990 Sep 09; 10(3):159-66. PubMed ID: 2144533
    [Abstract] [Full Text] [Related]

  • 12. [Digestive system disease as manifestation of the pleiotropic action of genes in mitochondrial dysfunction].
    Hrechanina OIa, Hrechanina IuB, Husar VA, Molodan LV.
    Lik Sprava; 2014 Nov 09; (11):29-39. PubMed ID: 25528830
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial defects in neurodegenerative disease.
    Wallace DC.
    Ment Retard Dev Disabil Res Rev; 2001 Nov 09; 7(3):158-66. PubMed ID: 11553931
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  • 18. 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 Nov 09; 4(2):132-5. PubMed ID: 7981717
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  • 20. A patient with two mitochondrial DNA mutations causing PEO and LHON.
    Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A.
    Eur J Med Genet; 2009 Nov 09; 52(1):47-8. PubMed ID: 19015050
    [Abstract] [Full Text] [Related]

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