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PUBMED FOR HANDHELDS

Journal Abstract Search


159 related items for PubMed ID: 14678805

  • 1. Relation of CTG expansion and clinical variables to electrocardiogram conduction abnormalities and sudden death in patients with myotonic dystrophy.
    Sabovic M, Medica I, Logar N, Mandić E, Zidar J, Peterlin B.
    Neuromuscul Disord; 2003 Dec; 13(10):822-6. PubMed ID: 14678805
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  • 2. Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry.
    Chong-Nguyen C, Wahbi K, Algalarrondo V, Bécane HM, Radvanyi-Hoffman H, Arnaud P, Furling D, Lazarus A, Bassez G, Béhin A, Fayssoil A, Laforêt P, Stojkovic T, Eymard B, Duboc D.
    Circ Cardiovasc Genet; 2017 Jun; 10(3):. PubMed ID: 28611030
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  • 3. Cardiac involvement and CTG expansion in myotonic dystrophy.
    Merlevede K, Vermander D, Theys P, Legius E, Ector H, Robberecht W.
    J Neurol; 2002 Jun; 249(6):693-8. PubMed ID: 12111301
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  • 5. DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model.
    Berul CI, Maguire CT, Aronovitz MJ, Greenwood J, Miller C, Gehrmann J, Housman D, Mendelsohn ME, Reddy S.
    J Clin Invest; 1999 Feb; 103(4):R1-7. PubMed ID: 10021468
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  • 6. Usefulness of clinical and electrocardiographic data for predicting adverse cardiac events in patients with myotonic dystrophy.
    Breton R, Mathieu J.
    Can J Cardiol; 2009 Feb; 25(2):e23-7. PubMed ID: 19214296
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  • 8. Progressive atrioventricular conduction block in a mouse myotonic dystrophy model.
    Berul CI, Maguire CT, Gehrmann J, Reddy S.
    J Interv Card Electrophysiol; 2000 Jun; 4(2):351-8. PubMed ID: 10936001
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  • 9. Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1.
    Salvatori S, Fanin M, Trevisan CP, Furlan S, Reddy S, Nagy JI, Angelini C.
    Neurol Sci; 2005 Oct; 26(4):235-42. PubMed ID: 16193250
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  • 10. Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy.
    Melacini P, Villanova C, Menegazzo E, Novelli G, Danieli G, Rizzoli G, Fasoli G, Angelini C, Buja G, Miorelli M.
    J Am Coll Cardiol; 1995 Jan; 25(1):239-45. PubMed ID: 7798509
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  • 11. Diastolic heart dysfunction is correlated with CTG repeat length in myotonic dystrophy type 1.
    Park JS, Kim N, Park D.
    Neurol Sci; 2018 Nov; 39(11):1935-1943. PubMed ID: 30094526
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  • 16. [Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion].
    Spranger M, Janssen B, Rating D, Spranger S.
    Nervenarzt; 1999 Feb; 70(2):131-5. PubMed ID: 10098148
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  • 18. Correlations between individual clinical manifestations and CTG repeat amplification in myotonic dystrophy.
    Marchini C, Lonigro R, Verriello L, Pellizzari L, Bergonzi P, Damante G.
    Clin Genet; 2000 Jan; 57(1):74-82. PubMed ID: 10733240
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  • 19. The heart and cardiac pacing in Steinert disease.
    Nigro G, Papa AA, Politano L.
    Acta Myol; 2012 Oct; 31(2):110-6. PubMed ID: 23097601
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  • 20. Heart rate variability declines with increasing age and CTG repeat length in patients with myotonic dystrophy type 1.
    Hardin BA, Lowe MR, Bhakta D, Groh WJ.
    Ann Noninvasive Electrocardiol; 2003 Jul; 8(3):227-32. PubMed ID: 14510658
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