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Journal Abstract Search

360 related items for PubMed ID: 10852545

  • 1. Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
    Nishino I, Spinazzola A, Papadimitriou A, Hammans S, Steiner I, Hahn CD, Connolly AM, Verloes A, Guimarães J, Maillard I, Hamano H, Donati MA, Semrad CE, Russell JA, Andreu AL, Hadjigeorgiou GM, Vu TH, Tadesse S, Nygaard TG, Nonaka I, Hirano I, Bonilla E, Rowland LP, DiMauro S, Hirano M.
    Ann Neurol; 2000 Jun; 47(6):792-800. PubMed ID: 10852545
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  • 2. A novel ECGF1 mutation in a Thai patient with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Kintarak J, Liewluck T, Sangruchi T, Hirano M, Kulkantrakorn K, Muengtaweepongsa S.
    Clin Neurol Neurosurg; 2007 Sep; 109(7):613-6. PubMed ID: 17544574
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  • 8. Mitochondrial neurogastrointestinal encephalomyopathy: novel pathogenic mutations in thymidine phosphorylase gene in two Italian brothers.
    Libernini L, Lupis C, Mastrangelo M, Carrozzo R, Santorelli FM, Inghilleri M, Leuzzi V.
    Neuropediatrics; 2012 Aug; 43(4):201-8. PubMed ID: 22618301
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  • 9. Thymidine phosphorylase mutations cause instability of mitochondrial DNA.
    Hirano M, Lagier-Tourenne C, Valentino ML, Martí R, Nishigaki Y.
    Gene; 2005 Jul 18; 354():152-6. PubMed ID: 15975738
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  • 12. MNGIE: from nuclear DNA to mitochondrial DNA.
    Nishino I, Spinazzola A, Hirano M.
    Neuromuscul Disord; 2001 Jan 18; 11(1):7-10. PubMed ID: 11166160
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  • 20. A novel TYMP mutation in a French Canadian patient with mitochondrial neurogastrointestinal encephalomyopathy.
    Laforce R, Valdmanis PN, Dupré N, Rouleau GA, Turgeon AF, Savard M.
    Clin Neurol Neurosurg; 2009 Oct 18; 111(8):691-4. PubMed ID: 19523753
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