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Journal Abstract Search

107 related items for PubMed ID: 11596344

  • 21. Mitochondrial encephalomyopathies: an update.
    DiMauro S, Hirano M.
    Neuromuscul Disord; 2005 Apr; 15(4):276-86. PubMed ID: 15792866
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  • 23. [Mitochondrial disorders: a classification for the 21st century].
    Andreu AL, Gonzalo-Sanz R.
    Neurologia; 2004 Apr; 19(1):15-22. PubMed ID: 14762729
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  • 25. The contribution of mitochondrial dysfunction to a gene-environment model of Guamanian ALS and PD.
    Lynch D, Wanglund C, Spathis R, Chan CW, Reiff DM, Lum JK, Garruto RM.
    Mitochondrion; 2008 Mar; 8(2):109-16. PubMed ID: 18054291
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  • 28. Mitochondrial oxidative phosphorylation disorders presenting in neonates: clinical manifestations and enzymatic and molecular diagnoses.
    Gibson K, Halliday JL, Kirby DM, Yaplito-Lee J, Thorburn DR, Boneh A.
    Pediatrics; 2008 Nov; 122(5):1003-8. PubMed ID: 18977979
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  • 37. [Mitochondrial diseases. Clinical features, investigation and genetics].
    Østergaard E, Wibrand F, Horn N, Brøndum-Nielsen K.
    Ugeskr Laeger; 2003 Feb 10; 165(7):663-8. PubMed ID: 12617042
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  • 39. Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseases.
    Debray FG, Lambert M, Chevalier I, Robitaille Y, Decarie JC, Shoubridge EA, Robinson BH, Mitchell GA.
    Pediatrics; 2007 Apr 10; 119(4):722-33. PubMed ID: 17403843
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  • 40. [MNGIE--thymidine phosphorylase deficiency].
    Nishino I, Hirano M.
    Nihon Rinsho; 2002 Apr 10; 60 Suppl 4():349-52. PubMed ID: 12013883
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