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Journal Abstract Search

464 related items for PubMed ID: 9924029

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  • 22. [Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)].
    Honzík T, Tesarová M, Hansíková H, Krijt J, Benes P, Zámecník J, Wenchich L, Zeman J.
    Cas Lek Cesk; 2006; 145(8):665-70. PubMed ID: 16995425
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  • 23. 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; 111(8):691-4. PubMed ID: 19523753
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  • 27. Thymidine phosphorylase gene mutations cause mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Hirano M, Nishino I, Nishigaki Y, Martí R.
    Intern Med; 2006 Oct; 45(19):1103. PubMed ID: 17077575
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  • 30. Liver as a source for thymidine phosphorylase replacement in mitochondrial neurogastrointestinal encephalomyopathy.
    Boschetti E, D'Alessandro R, Bianco F, Carelli V, Cenacchi G, Pinna AD, Del Gaudio M, Rinaldi R, Stanghellini V, Pironi L, Rhoden K, Tugnoli V, Casali C, De Giorgio R.
    PLoS One; 2014 Oct; 9(5):e96692. PubMed ID: 24802030
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  • 32. Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy.
    Van Goethem G, Schwartz M, Löfgren A, Dermaut B, Van Broeckhoven C, Vissing J.
    Eur J Hum Genet; 2003 Jul; 11(7):547-9. PubMed ID: 12825077
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  • 33. 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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  • 35. Discovery profiling and bioinformatics analysis of serum microRNA in Mitochondrial NeuroGastroIntestinal Encephalomyopathy (MNGIE).
    Levene M, Enguita FJ, Bax BE.
    Nucleosides Nucleotides Nucleic Acids; 2018 Aug; 37(11):618-629. PubMed ID: 30587073
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  • 36. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): case report with a new mutation.
    Bariş Z, Eminoğlu T, Dalgiç B, Tümer L, Hasanoğlu A.
    Eur J Pediatr; 2010 Nov; 169(11):1375-8. PubMed ID: 20585803
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  • 39. Phenotypic variability in a Spanish family with MNGIE.
    Gamez J, Ferreiro C, Accarino ML, Guarner L, Tadesse S, Martí RA, Andreu AL, Raguer N, Cervera C, Hirano M.
    Neurology; 2002 Aug 13; 59(3):455-7. PubMed ID: 12177387
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  • 40. Definitive diagnosis of mitochondrial neurogastrointestinal encephalomyopathy by biochemical assays.
    Martí R, Spinazzola A, Tadesse S, Nishino I, Nishigaki Y, Hirano M.
    Clin Chem; 2004 Jan 13; 50(1):120-4. PubMed ID: 14633909
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