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PUBMED FOR HANDHELDS

Journal Abstract Search

254 related items for PubMed ID: 11579420

  • 1.
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  • 2. Renal disease and mitochondrial genetics.
    Rötig A.
    J Nephrol; 2003; 16(2):286-92. PubMed ID: 12768079
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  • 6. Genetic bases of mitochondrial respiratory chain disorders.
    Rötig A.
    Diabetes Metab; 2010 Apr; 36(2):97-107. PubMed ID: 20093061
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  • 7. Cytochrome c oxidase deficiency.
    Shoubridge EA.
    Am J Med Genet; 2001 Apr; 106(1):46-52. PubMed ID: 11579424
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  • 8. [Diseases of the human mitochondrial oxidative phosphorylation system].
    Ruiz-Pesini E, López-Gallardo E, Dahmani Y, Herrero MD, Solano A, Díez-Sánchez C, López-Pérez M, Montoya J.
    Rev Neurol; 2001 Apr; 43(7):416-24. PubMed ID: 17006861
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  • 10. Genetics of mitochondrial respiratory chain deficiencies.
    Rötig A.
    Rev Neurol (Paris); 2014 May; 170(5):309-22. PubMed ID: 24798924
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  • 13. [Mitochondrial disorders: a classification for the 21st century].
    Andreu AL, Gonzalo-Sanz R.
    Neurologia; 2004 May; 19(1):15-22. PubMed ID: 14762729
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  • 14. The diagnosis of mitochondrial muscle disease.
    Taylor RW, Schaefer AM, Barron MJ, McFarland R, Turnbull DM.
    Neuromuscul Disord; 2004 Apr; 14(4):237-45. PubMed ID: 15019701
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  • 16. Mitochondria and degenerative disorders.
    Orth M, Schapira AH.
    Am J Med Genet; 2001 Apr; 106(1):27-36. PubMed ID: 11579422
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  • 19. Diseases caused by nuclear genes affecting mtDNA stability.
    Suomalainen A, Kaukonen J.
    Am J Med Genet; 2001 Apr; 106(1):53-61. PubMed ID: 11579425
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  • 20. Mitochondrial dysfunction and the role of the non-specialist laboratory.
    Hancock MR.
    Ann Clin Biochem; 2002 Sep; 39(Pt 5):456-63. PubMed ID: 12227851
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