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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

382 related items for PubMed ID: 18306244

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  • 7. Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase.
    Pitkanen S, Robinson BH.
    J Clin Invest; 1996 Jul 15; 98(2):345-51. PubMed ID: 8755643
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  • 8. Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome.
    Ostergaard E, Rodenburg RJ, van den Brand M, Thomsen LL, Duno M, Batbayli M, Wibrand F, Nijtmans L.
    J Med Genet; 2011 Nov 15; 48(11):737-40. PubMed ID: 21617257
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  • 11. Normal muscle respiratory chain enzymes can complicate mitochondrial disease diagnosis.
    Oglesbee D, Freedenberg D, Kramer KA, Anderson BD, Hahn SH.
    Pediatr Neurol; 2006 Oct 15; 35(4):289-92. PubMed ID: 16996407
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  • 15. Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.
    Procaccio V, Mousson B, Beugnot R, Duborjal H, Feillet F, Putet G, Pignot-Paintrand I, Lombès A, De Coo R, Smeets H, Lunardi J, Issartel JP.
    J Clin Invest; 1999 Jul 15; 104(1):83-92. PubMed ID: 10393702
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  • 17. Progressive encephalopathy and complex I deficiency associated with mutations in MTND1.
    Moslemi AR, Darin N, Tulinius M, Wiklund LM, Holme E, Oldfors A.
    Neuropediatrics; 2008 Feb 15; 39(1):24-8. PubMed ID: 18504678
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  • 20. [A case of Leigh syndrome associated with respiratory chain complex I deficiency due to mitochondrial gene 13513G>A mutation].
    Wei XQ, Kong QP, Zhang Y, Yang YL, Chang XZ, Qi Y, Qi ZY, Xiao JX, Qin J, Wu XR.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 May 15; 11(5):333-6. PubMed ID: 19470250
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