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Journal Abstract Search

280 related items for PubMed ID: 17105751

  • 21.
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  • 24. Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.
    van Tintelen JP, Entius MM, Bhuiyan ZA, Jongbloed R, Wiesfeld AC, Wilde AA, van der Smagt J, Boven LG, Mannens MM, van Langen IM, Hofstra RM, Otterspoor LC, Doevendans PA, Rodriguez LM, van Gelder IC, Hauer RN.
    Circulation; 2006 Apr 04; 113(13):1650-8. PubMed ID: 16567567
    [Abstract] [Full Text] [Related]

  • 25. Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations.
    Bauce B, Basso C, Rampazzo A, Beffagna G, Daliento L, Frigo G, Malacrida S, Settimo L, Danieli G, Thiene G, Nava A.
    Eur Heart J; 2005 Aug 04; 26(16):1666-75. PubMed ID: 15941723
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  • 26. Correlation of ventricular arrhythmias with genotype in arrhythmogenic right ventricular cardiomyopathy.
    Bao J, Wang J, Yao Y, Wang Y, Fan X, Sun K, He DS, Marcus FI, Zhang S, Hui R, Song L.
    Circ Cardiovasc Genet; 2013 Dec 04; 6(6):552-6. PubMed ID: 24125834
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  • 27. Novel plakophilin2 mutation: three-generation family with arrhythmogenic right ventricular cardiomyopathy.
    Aneq MÅ, Fluur C, Rehnberg M, Söderkvist P, Engvall J, Nylander E, Gunnarsson C.
    Scand Cardiovasc J; 2012 Apr 04; 46(2):72-5. PubMed ID: 22035158
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  • 28. Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family.
    Kannankeril PJ, Bhuiyan ZA, Darbar D, Mannens MM, Wilde AA, Roden DM.
    Heart Rhythm; 2006 Aug 04; 3(8):939-44. PubMed ID: 16876743
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  • 29. In vitro analysis of arrhythmogenic cardiomyopathy associated desmoglein-2 (DSG2) mutations reveals diverse glycosylation patterns.
    Debus JD, Milting H, Brodehl A, Kassner A, Anselmetti D, Gummert J, Gaertner-Rommel A.
    J Mol Cell Cardiol; 2019 Apr 04; 129():303-313. PubMed ID: 30885746
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  • 30. Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotype.
    Vatta M, Marcus F, Towbin JA.
    Eur Heart J; 2007 Mar 04; 28(5):529-30. PubMed ID: 17303588
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  • 31. Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy.
    Lahtinen AM, Lehtonen E, Marjamaa A, Kaartinen M, Heliö T, Porthan K, Oikarinen L, Toivonen L, Swan H, Jula A, Peltonen L, Palotie A, Salomaa V, Kontula K.
    Heart Rhythm; 2011 Aug 04; 8(8):1214-21. PubMed ID: 21397041
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  • 32. Large Genomic Rearrangements of Desmosomal Genes in Italian Arrhythmogenic Cardiomyopathy Patients.
    Pilichou K, Lazzarini E, Rigato I, Celeghin R, De Bortoli M, Perazzolo Marra M, Cason M, Jongbloed J, Calore M, Rizzo S, Regazzo D, Poloni G, Iliceto S, Daliento L, Delise P, Corrado D, Van Tintelen JP, Thiene G, Rampazzo A, Basso C, Bauce B, Lorenzon A, Occhi G.
    Circ Arrhythm Electrophysiol; 2017 Oct 04; 10(10):. PubMed ID: 29038103
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  • 33. Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
    Groeneweg JA, Ummels A, Mulder M, Bikker H, van der Smagt JJ, van Mil AM, Homfray T, Post JG, Elvan A, van der Heijden JF, Houweling AC, Jongbloed JD, Wilde AA, van Tintelen JP, Hauer RN, Dooijes D.
    Heart Rhythm; 2014 Nov 04; 11(11):2010-7. PubMed ID: 25087486
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  • 35. Arrhythmogenic Right Ventricular Cardiomyopathy Presenting as Clinical Myocarditis in Women.
    Scheel PJ, Murray B, Tichnell C, James CA, Tandri H, Calkins H, Chelko SP, Gilotra NA.
    Am J Cardiol; 2021 Apr 15; 145():128-134. PubMed ID: 33460606
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  • 37. A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy.
    Posch MG, Posch MJ, Geier C, Erdmann B, Mueller W, Richter A, Ruppert V, Pankuweit S, Maisch B, Perrot A, Buttgereit J, Dietz R, Haverkamp W, Ozcelik C.
    Mol Genet Metab; 2008 Apr 15; 95(1-2):74-80. PubMed ID: 18678517
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  • 38. Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy.
    Noor Ul Ayan H, Ali PS, Korejo AA, Thiele H, Nürnberg P, Tariq M, Jamal SZ, Erdmann J, Ahmad I.
    Clin Genet; 2023 Aug 15; 104(2):266-268. PubMed ID: 36843528
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  • 39. Characteristics of Patients With Arrhythmogenic Left Ventricular Cardiomyopathy: Combining Genetic and Histopathologic Findings.
    Casella M, Gasperetti A, Sicuso R, Conte E, Catto V, Sommariva E, Bergonti M, Vettor G, Rizzo S, Pompilio G, Andreini D, Saguner AM, Duru F, Natale A, Thiene G, Basso C, Dello Russo A, Tondo C.
    Circ Arrhythm Electrophysiol; 2020 Dec 15; 13(12):e009005. PubMed ID: 33197325
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  • 40. Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin.
    La Gerche A, Robberecht C, Kuiperi C, Nuyens D, Willems R, de Ravel T, Matthijs G, Heidbüchel H.
    Heart; 2010 Aug 15; 96(16):1268-74. PubMed ID: 20525856
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