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Journal Abstract Search

136 related items for PubMed ID: 24726585

  • 1. Diagnosis of mitochondrial neurogastrointestinal encephalomyopathy: proposal of a clinical algorithm.
    Zimmer V, Hirano M, Zimmer A, Lammert F.
    Dig Liver Dis; 2014 Jul; 46(7):664-5. PubMed ID: 24726585
    [No Abstract] [Full Text] [Related]

  • 2. Unexplained gastrointestinal symptoms: think mitochondrial disease.
    Chapman TP, Hadley G, Fratter C, Cullen SN, Bax BE, Bain MD, Sapsford RA, Poulton J, Travis SP.
    Dig Liver Dis; 2014 Jan; 46(1):1-8. PubMed ID: 23768727
    [Abstract] [Full Text] [Related]

  • 3. Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy.
    Garone C, Tadesse S, Hirano M.
    Brain; 2011 Nov; 134(Pt 11):3326-32. PubMed ID: 21933806
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  • 5. [Mitochondrial neurogastrointestinal encephalopathy syndrome].
    Grechanina IuB.
    Lik Sprava; 2014 Nov; (11):146-8. PubMed ID: 25528855
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  • 7. Tachyduodenia in mitochondrial neurogastrointestinal encephalomyopathy.
    Scheffer RC, Smout AJ.
    Neurogastroenterol Motil; 2011 May; 23(5):408-10. PubMed ID: 21481099
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  • 8. Mitochondrial DNA mutations and mitochondrial dysfunction in epilepsy.
    Cock H, Schapira AH.
    Epilepsia; 1999 May; 40 Suppl 3():33-40. PubMed ID: 10446749
    [No Abstract] [Full Text] [Related]

  • 9. [Masks hiding mitochondrial neurogastrointestinal encephalomyopathy. Case report].
    Maev IV, Kolmakova EV, Bardakov SN, Deev RV, Krivolapov YA, Kotkas IE, Manushina EA, Kurbatov SA, Tsygankova PG, Emelin AM, Bakulina NV.
    Ter Arkh; 2022 Oct 12; 94(8):992-998. PubMed ID: 36286980
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  • 10. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder.
    Hirano M, Silvestri G, Blake DM, Lombes A, Minetti C, Bonilla E, Hays AP, Lovelace RE, Butler I, Bertorini TE.
    Neurology; 1994 Apr 12; 44(4):721-7. PubMed ID: 8164833
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  • 11. Mitochondrial neurogastrointestinal encephalomyopathy: case report.
    Çolak Y, Tuncer İ, Çağlar E, Barutçu D, Ulaşoğlu C, Kiziltaş Ş.
    Turk J Gastroenterol; 2010 Sep 12; 21(3):305-7. PubMed ID: 20931438
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  • 12. [Current status of mitochondrial diseases].
    Lombès A.
    Rev Neurol (Paris); 1998 Apr 12; 154(3):261-4. PubMed ID: 9773055
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  • 14. Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome.
    Slama A, Lacroix C, Plante-Bordeneuve V, Lombès A, Conti M, Reimund JM, Auxenfants E, Crenn P, Laforêt P, Joannard A, Seguy D, Pillant H, Joly P, Haut S, Messing B, Said G, Legrand A, Guiochon-Mantel A.
    Mol Genet Metab; 2005 Apr 12; 84(4):326-31. PubMed ID: 15781193
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  • 15. Mitochondrial myopathies and encephalomyopathies.
    Schapira AH, Cock HR.
    Eur J Clin Invest; 1999 Oct 12; 29(10):886-98. PubMed ID: 10583431
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  • 17. 163rd ENMC International Workshop: nucleoid and nucleotide biology in syndromes of mitochondrial DNA depletion myopathy 12-14 December 2008, Naarden, The Netherlands.
    Poulton J, Holt IJ.
    Neuromuscul Disord; 2009 Jun 12; 19(6):439-43. PubMed ID: 19464176
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  • 20. Delayed onset of recurrent episodes of acute pseudo-obstruction in a patient with mitochondrial myopathy.
    Lok SC, Courtney ED, Tang TY, Bekdash B.
    Int J Colorectal Dis; 2009 Aug 12; 24(8):991-2. PubMed ID: 19381656
    [No Abstract] [Full Text] [Related]

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