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Journal Abstract Search


204 related items for PubMed ID: 8884575

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  • 2. Clinical spectrum and diagnosis of mitochondrial disorders.
    Munnich A, Rustin P.
    Am J Med Genet; 2001; 106(1):4-17. PubMed ID: 11579420
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  • 5. Genetics of mitochondrial respiratory chain deficiencies.
    Rötig A.
    Rev Neurol (Paris); 2014 May; 170(5):309-22. PubMed ID: 24798924
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  • 6. Renal disease and mitochondrial genetics.
    Rötig A.
    J Nephrol; 2003 May; 16(2):286-92. PubMed ID: 12768079
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  • 11. The effect of small molecules on nuclear-encoded translation diseases.
    Soiferman D, Ayalon O, Weissman S, Saada A.
    Biochimie; 2014 May; 100():184-91. PubMed ID: 24012549
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  • 15. Disorders of the mitochondria.
    Treem WR, Sokol RJ.
    Semin Liver Dis; 1998 May; 18(3):237-53. PubMed ID: 9773424
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  • 16. Disorders of the electron transport chain.
    Adams PL, Turnbull DM.
    J Inherit Metab Dis; 1996 May; 19(4):463-9. PubMed ID: 8884570
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  • 17. Biogenesis of mitochondria and genetics of mitochondrial defects.
    Kroon AM, Van den Bogert C.
    J Inherit Metab Dis; 1987 May; 10 Suppl 1():54-61. PubMed ID: 2446047
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  • 18. Genetic control of oxidative phosphorylation and experimental models of defects.
    Trounce I.
    Hum Reprod; 2000 Jul; 15 Suppl 2():18-27. PubMed ID: 11041510
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  • 19. [Application of new techniques for locating the underlying molecular defects in patients with disorders of oxidative phosphorylation].
    Van Coster R, Smet J.
    Verh K Acad Geneeskd Belg; 2007 Jul; 69(4):197-211. PubMed ID: 17821958
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  • 20. [Enzyme complex defects of the mitochondrial respiratory chain].
    Rubio JC, Martín MA, del Hoyo P, de Bustos F, Campos Y, Arenas J.
    Rev Neurol; 1998 Apr; 26 Suppl 1():S15-20. PubMed ID: 9810586
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