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    Results: 1 to 50 of 439

    1.

    Pacemaker Therapy in Hypertrophic Obstructive Cardiomyopathy: Still Awaiting the Evidence.

    McKenna WJ, Kaski JP.

    Rev Esp Cardiol. 2009 Nov;62(11):1217-1220. English, Spanish. No abstract available. PMID: 19889331 [PubMed - as supplied by publisher]Related articlesFree article

    2.

    Splicing and dilated cardiomyopathy one gene to rule them all?

    Macrae CA, McKenna WJ.

    J Am Coll Cardiol. 2009 Sep 1;54(10):942-3. No abstract available. PMID: 19712805 [PubMed - indexed for MEDLINE]Related articles

    3.

    Exercise-induced ventricular arrhythmias and risk of sudden cardiac death in patients with hypertrophic cardiomyopathy.

    Gimeno JR, Tomé-Esteban M, Lofiego C, Hurtado J, Pantazis A, Mist B, Lambiase P, McKenna WJ, Elliott PM.

    Eur Heart J. 2009 Nov;30(21):2599-605. Epub 2009 Aug 17.PMID: 19689975 [PubMed - in process]Related articles

    4.

    Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance.

    Seebohm B, Matinmehr F, Köhler J, Francino A, Navarro-Lopéz F, Perrot A, Ozcelik C, McKenna WJ, Brenner B, Kraft T.

    Biophys J. 2009 Aug 5;97(3):806-24.PMID: 19651039 [PubMed - indexed for MEDLINE]Related articles

    5.

    ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene.

    Moulik M, Vatta M, Witt SH, Arola AM, Murphy RT, McKenna WJ, Boriek AM, Oka K, Labeit S, Bowles NE, Arimura T, Kimura A, Towbin JA.

    J Am Coll Cardiol. 2009 Jul 21;54(4):325-33.PMID: 19608030 [PubMed - indexed for MEDLINE]Related articles

    6.

    Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency.

    Marston S, Copeland O, Jacques A, Livesey K, Tsang V, McKenna WJ, Jalilzadeh S, Carballo S, Redwood C, Watkins H.

    Circ Res. 2009 Jul 31;105(3):219-22. Epub 2009 Jul 2.PMID: 19574547 [PubMed - indexed for MEDLINE]Related articles

    7.

    High-density substrate mapping in Brugada syndrome: combined role of conduction and repolarization heterogeneities in arrhythmogenesis.

    Lambiase PD, Ahmed AK, Ciaccio EJ, Brugada R, Lizotte E, Chaubey S, Ben-Simon R, Chow AW, Lowe MD, McKenna WJ.

    Circulation. 2009 Jul 14;120(2):106-17, 1-4. Epub 2009 Jun 29.PMID: 19564561 [PubMed - indexed for MEDLINE]Related articles

    8.

    A new diagnostic test for arrhythmogenic right ventricular cardiomyopathy.

    Asimaki A, Tandri H, Huang H, Halushka MK, Gautam S, Basso C, Thiene G, Tsatsopoulou A, Protonotarios N, McKenna WJ, Calkins H, Saffitz JE.

    N Engl J Med. 2009 Mar 12;360(11):1075-84.PMID: 19279339 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Unique epidermolytic bullous dermatosis with associated lethal cardiomyopathy related to novel desmoplakin mutations.

    Asimaki A, Syrris P, Ward D, Guereta LG, Saffitz JE, McKenna WJ.

    J Cutan Pathol. 2009 May;36(5):553-9. Epub 2008 Oct 29.PMID: 19178614 [PubMed - indexed for MEDLINE]Related articles

    10.

    Syncope in an adolescent: a case of conflicting tests and dual pathology.

    Sen-Chowdhry S, Sevdalis E, Wage R, Mist B, Kilner PJ, McKenna WJ.

    Int J Clin Pract. 2008 Nov;62(11):1803-7. No abstract available. PMID: 19143866 [PubMed - indexed for MEDLINE]Related articles

    11.

    The emerging role of cardiovascular magnetic resonance in refining the diagnosis of hypertrophic cardiomyopathy.

    Moon JC, McKenna WJ.

    Nat Clin Pract Cardiovasc Med. 2009 Mar;6(3):166-7. Epub 2009 Jan 13.PMID: 19139744 [PubMed - indexed for MEDLINE]Related articles

    12.

    Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity.

    Sen-Chowdhry S, Syrris P, Prasad SK, Hughes SE, Merrifield R, Ward D, Pennell DJ, McKenna WJ.

    J Am Coll Cardiol. 2008 Dec 16;52(25):2175-87.PMID: 19095136 [PubMed - indexed for MEDLINE]Related articles

    13.

    From Teare to the present day: a fifty year odyssey in hypertrophic cardiomyopathy, a paradigm for the logic of the discovery process.

    McKenna WJ, Sen-Chowdhry S.

    Rev Esp Cardiol. 2008 Dec;61(12):1239-44. English, Spanish. No abstract available. PMID: 19080961 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.

    Simpson MA, Mansour S, Ahnood D, Kalidas K, Patton MA, McKenna WJ, Behr ER, Crosby AH.

    Cardiology. 2009;113(1):28-34. Epub 2008 Oct 29.PMID: 18957847 [PubMed - indexed for MEDLINE]Related articles

    15.

    Episodic syncope in hypertrophic cardiomyopathy: evidence for inappropriate vasodilation.

    Prasad K, Williams L, Campbell R, Elliott PM, McKenna WJ, Frenneaux M.

    Heart. 2008 Oct;94(10):1312-7. Epub 2008 Jul 24.PMID: 18653581 [PubMed - indexed for MEDLINE]Related articles

    16.

    The genetics of hypertrophic cardiomyopathy: Teare redux.

    Watkins H, Ashrafian H, McKenna WJ.

    Heart. 2008 Oct;94(10):1264-8. Epub 2008 Jul 24. Review. No abstract available. PMID: 18653576 [PubMed - indexed for MEDLINE]Related articles

    17.

    [Classification of the cardiomyopathies]

    Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, Dubourg O, Kühl U, Maisch B, McKenna WJ, Monserrat L, Pankuwelt S, Rapezzi C, Seferovic P, Tavazzi L, Keren A.

    Kardiol Pol. 2008 May;66(5):533-40, discussion 541-2. Review. Polish. No abstract available. PMID: 18630392 [PubMed - indexed for MEDLINE]Related articles

    18.

    Myosin binding protein C phosphorylation in normal, hypertrophic and failing human heart muscle.

    Jacques AM, Copeland O, Messer AE, Gallon CE, King K, McKenna WJ, Tsang VT, Marston SB.

    J Mol Cell Cardiol. 2008 Aug;45(2):209-16. Epub 2008 Jun 4.PMID: 18573260 [PubMed - indexed for MEDLINE]Related articles

    19.

    Non-invasive risk stratification in hypertrophic cardiomyopathy: don't throw out the baby with the bathwater.

    Sen-Chowdhry S, McKenna WJ.

    Eur Heart J. 2008 Jul;29(13):1600-2. Epub 2008 Jun 5. No abstract available. PMID: 18539587 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

    Behr ER, Dalageorgou C, Christiansen M, Syrris P, Hughes S, Tome Esteban MT, Rowland E, Jeffery S, McKenna WJ.

    Eur Heart J. 2008 Jul;29(13):1670-80. Epub 2008 May 27.PMID: 18508782 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    The new European definition of cardiomyopathies: which space for muscle dystrophies? reply.

    Elliott P; and on behalf of the following co-authors:, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, Dubourg O, Kühl U, Maisch B, McKenna WJ, Monserrat L, Pankuweit S, Rapezzi C, Seferovic P, Tavazzi L, Keren A.

    Eur Heart J. 2008 May 15. [Epub ahead of print] No abstract available. PMID: 18487209 [PubMed - as supplied by publisher]Related articles

    22.

    Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.

    Kaski JP, Syrris P, Burch M, Tomé-Esteban MT, Fenton M, Christiansen M, Andersen PS, Sebire N, Ashworth M, Deanfield JE, McKenna WJ, Elliott PM.

    Heart. 2008 Nov;94(11):1478-84. Epub 2008 May 8.PMID: 18467357 [PubMed - indexed for MEDLINE]Related articles

    23.

    The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy.

    Jacques AM, Briceno N, Messer AE, Gallon CE, Jalilzadeh S, Garcia E, Kikonda-Kanda G, Goddard J, Harding SE, Watkins H, Esteban MT, Tsang VT, McKenna WJ, Marston SB.

    Cardiovasc Res. 2008 Aug 1;79(3):481-91. Epub 2008 Apr 14.PMID: 18411228 [PubMed - indexed for MEDLINE]Related articlesFree article

    24.

    Effect of biventricular pacing on symptoms and cardiac remodelling in patients with end-stage hypertrophic cardiomyopathy.

    Rogers DP, Marazia S, Chow AW, Lambiase PD, Lowe MD, Frenneaux M, McKenna WJ, Elliott PM.

    Eur J Heart Fail. 2008 May;10(5):507-13. Epub 2008 Apr 10.PMID: 18406204 [PubMed - indexed for MEDLINE]Related articles

    25.

    Left ventricular noncompaction and cardiomyopathy: cause, contributor, or epiphenomenon?

    Sen-Chowdhry S, McKenna WJ.

    Curr Opin Cardiol. 2008 May;23(3):171-5. Review.PMID: 18382203 [PubMed - indexed for MEDLINE]Related articles

    26.

    What do tachycardiomyopathy belong to? Reply.

    Elliott P; and on behalf of the following co-authors:, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, Dubourg O, Kühl U, Maisch B, McKenna WJ, Monserrat L, Pankuweit S, Rapezzi C, Seferovic P, Tavazzi L, Keren A.

    Eur Heart J. 2008 Mar 27. [Epub ahead of print] No abstract available. PMID: 18372298 [PubMed - as supplied by publisher]Related articles

    27.

    Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations.

    Frank-Hansen R, Page SP, Syrris P, McKenna WJ, Christiansen M, Andersen PS.

    Eur J Hum Genet. 2008 Sep;16(9):1062-9. Epub 2008 Mar 12.PMID: 18337725 [PubMed - indexed for MEDLINE]Related articlesFree article

    28.

    The utility of magnetic resonance imaging in the evaluation of arrhythmogenic right ventricular cardiomyopathy.

    Sen-Chowdhry S, McKenna WJ.

    Curr Opin Cardiol. 2008 Jan;23(1):38-45. Review.PMID: 18281826 [PubMed - indexed for MEDLINE]Related articles

    29.

    Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression.

    Keren A, Syrris P, McKenna WJ.

    Nat Clin Pract Cardiovasc Med. 2008 Mar;5(3):158-68. Epub 2008 Jan 29. Review. Erratum in: Nat Clin Pract Cardiovasc Med. 2008 Nov;5(11):747. PMID: 18227814 [PubMed - indexed for MEDLINE]Related articles

    30.

    Psychiatric disorders in hypertrophic cardiomyopathy.

    Morgan JF, O'Donoghue AC, McKenna WJ, Schmidt MM.

    Gen Hosp Psychiatry. 2008 Jan-Feb;30(1):49-54.PMID: 18164940 [PubMed - indexed for MEDLINE]Related articles

    31.

    B-type natriuretic peptide predicts disease severity in children with hypertrophic cardiomyopathy.

    Kaski JP, Tomé-Esteban MT, Mead-Regan S, Pantazis A, Marek J, Deanfield JE, McKenna WJ, Elliott PM.

    Heart. 2008 Oct;94(10):1307-11. Epub 2007 Dec 10.PMID: 18070943 [PubMed - indexed for MEDLINE]Related articles

    32.

    Prevalence of exercise-induced left ventricular outflow tract obstruction in symptomatic patients with non-obstructive hypertrophic cardiomyopathy.

    Shah JS, Esteban MT, Thaman R, Sharma R, Mist B, Pantazis A, Ward D, Kohli SK, Page SP, Demetrescu C, Sevdalis E, Keren A, Pellerin D, McKenna WJ, Elliott PM.

    Heart. 2008 Oct;94(10):1288-94. Epub 2007 Nov 21.PMID: 18032461 [PubMed - indexed for MEDLINE]Related articles

    33.

    Diagnosis of left-ventricular non-compaction in patients with left-ventricular systolic dysfunction: time for a reappraisal of diagnostic criteria?

    Kohli SK, Pantazis AA, Shah JS, Adeyemi B, Jackson G, McKenna WJ, Sharma S, Elliott PM.

    Eur Heart J. 2008 Jan;29(1):89-95. Epub 2007 Nov 9.PMID: 17993472 [PubMed - indexed for MEDLINE]Related articlesFree article

    34.

    Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.

    Sen-Chowdhry S, Syrris P, McKenna WJ.

    J Am Coll Cardiol. 2007 Nov 6;50(19):1813-21. Epub 2007 Oct 24. Review.PMID: 17980246 [PubMed - indexed for MEDLINE]Related articles

    35.

    A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy.

    Asimaki A, Syrris P, Wichter T, Matthias P, Saffitz JE, McKenna WJ.

    Am J Hum Genet. 2007 Nov;81(5):964-73. Epub 2007 Sep 28.PMID: 17924338 [PubMed - indexed for MEDLINE]Related articlesFree article

    36.

    Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.

    Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, Dubourg O, Kühl U, Maisch B, McKenna WJ, Monserrat L, Pankuweit S, Rapezzi C, Seferovic P, Tavazzi L, Keren A.

    Eur Heart J. 2008 Jan;29(2):270-6. Epub 2007 Oct 4.PMID: 17916581 [PubMed - indexed for MEDLINE]Related articlesFree article

    37.

    Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome.

    Limongelli G, Pacileo G, Marino B, Digilio MC, Sarkozy A, Elliott P, Versacci P, Calabro P, De Zorzi A, Di Salvo G, Syrris P, Patton M, McKenna WJ, Dallapiccola B, Calabro R.

    Am J Cardiol. 2007 Aug 15;100(4):736-41. Epub 2007 Jun 27.PMID: 17697839 [PubMed - indexed for MEDLINE]Related articles

    38.

    Appropriate interpretation of the athlete's electrocardiogram saves lives as well as money.

    Corrado D, McKenna WJ.

    Eur Heart J. 2007 Aug;28(16):1920-2. Epub 2007 Jul 10. No abstract available. PMID: 17623679 [PubMed - indexed for MEDLINE]Related articlesFree article

    39.

    Variable interatrial conduction illustrated in a hypertrophic cardiomyopathy population.

    Holmqvist F, Platonov PG, Carlson J, Havmöller R, Waktare JE, McKenna WJ, Olsson SB, Meurling CJ.

    Ann Noninvasive Electrocardiol. 2007 Jul;12(3):227-36.PMID: 17617068 [PubMed - indexed for MEDLINE]Related articles

    40.

    Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.

    Kubo T, Gimeno JR, Bahl A, Steffensen U, Steffensen M, Osman E, Thaman R, Mogensen J, Elliott PM, Doi Y, McKenna WJ.

    J Am Coll Cardiol. 2007 Jun 26;49(25):2419-26. Epub 2007 Jun 11.PMID: 17599605 [PubMed - indexed for MEDLINE]Related articles

    41.

    Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression.

    Sen-Chowdhry S, Syrris P, Ward D, Asimaki A, Sevdalis E, McKenna WJ.

    Circulation. 2007 Apr 3;115(13):1710-20. Epub 2007 Mar 19.PMID: 17372169 [PubMed - indexed for MEDLINE]Related articlesFree article

    42.

    Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathy.

    Arola AM, Sanchez X, Murphy RT, Hasle E, Li H, Elliott PM, McKenna WJ, Towbin JA, Bowles NE.

    Mol Genet Metab. 2007 Apr;90(4):435-40. Epub 2007 Jan 24.PMID: 17254821 [PubMed - indexed for MEDLINE]Related articles

    43.

    Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death.

    Behr ER, Casey A, Sheppard M, Wright M, Bowker TJ, Davies MJ, McKenna WJ, Wood DA.

    Heart. 2007 May;93(5):601-5. Epub 2007 Jan 19.PMID: 17237131 [PubMed - indexed for MEDLINE]Related articles

    44.

    Prospective familial assessment in dilated cardiomyopathy: cardiac autoantibodies predict disease development in asymptomatic relatives.

    Caforio AL, Mahon NG, Baig MK, Tona F, Murphy RT, Elliott PM, McKenna WJ.

    Circulation. 2007 Jan 2;115(1):76-83. Epub 2006 Dec 18.PMID: 17179019 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    Cardiovascular magnetic resonance in arrhythmogenic right ventricular cardiomyopathy revisited: comparison with task force criteria and genotype.

    Sen-Chowdhry S, Prasad SK, Syrris P, Wage R, Ward D, Merrifield R, Smith GC, Firmin DN, Pennell DJ, McKenna WJ.

    J Am Coll Cardiol. 2006 Nov 21;48(10):2132-40. Epub 2006 Oct 31.PMID: 17113003 [PubMed - indexed for MEDLINE]Related articles

    46.

    Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease.

    Syrris P, Ward D, Asimaki A, Evans A, Sen-Chowdhry S, Hughes SE, McKenna WJ.

    Eur Heart J. 2007 Mar;28(5):581-8. Epub 2006 Nov 14.PMID: 17105751 [PubMed - indexed for MEDLINE]Related articlesFree article

    47.

    Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2.

    Syrris P, Ward D, Evans A, Asimaki A, Gandjbakhch E, Sen-Chowdhry S, McKenna WJ.

    Am J Hum Genet. 2006 Nov;79(5):978-84. Epub 2006 Sep 27.PMID: 17033975 [PubMed - indexed for MEDLINE]Related articlesFree article

    48.

    Functional effects of the DCM mutant Gly159Asp troponin C in skinned muscle fibres.

    Preston LC, Lipscomb S, Robinson P, Mogensen J, McKenna WJ, Watkins H, Ashley CC, Redwood CS.

    Pflugers Arch. 2007 Mar;453(6):771-6. Epub 2006 Sep 26.PMID: 17021793 [PubMed - indexed for MEDLINE]Related articles

    49.

    The variation of the sarcolipin gene (SLN) in atrial fibrillation, long QT syndrome and sudden arrhythmic death syndrome.

    Nyberg MT, Stoevring B, Behr ER, Ravn LS, McKenna WJ, Christiansen M.

    Clin Chim Acta. 2007 Jan;375(1-2):87-91. Epub 2006 Jun 22.PMID: 17010328 [PubMed - indexed for MEDLINE]Related articles

    50.

    Outcomes after implantable cardioverter-defibrillator treatment in children with hypertrophic cardiomyopathy.

    Pablo Kaski J, Tomé Esteban MT, Lowe M, Sporton S, Rees P, Deanfield JE, McKenna WJ, Elliott PM.

    Heart. 2007 Mar;93(3):372-4. Epub 2006 Aug 29. No abstract available. PMID: 16940391 [PubMed - indexed for MEDLINE]Related articles

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