Works matching IS 0195668X AND DT 2011 AND VI 32 AND IP 9
Results: 23
Working abroad: Professor Karen Sliwa discusses living and working in different environments.
- Published in:
- European Heart Journal, 2011, v. 32, n. 9, p. 1047
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European Heart for Children, an ESC-backed foundation for congenital heart disease, gets into gear.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1044
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- Article
The European Society of Cardiology ventures beyond Europe.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1041
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Benefits of surgery in obstructive hypertrophic cardiomyopathy: bring septal myectomy back for European patients.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1055, doi. 10.1093/eurheartj/ehr006
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CardioPulse Articles.
- Published in:
- European Heart Journal, 2011, v. 32, n. 9, p. 1041, doi. 10.1093/eurheartj/ehr081
- Publication type:
- Article
Adiponectin expression in patients with inflammatory cardiomyopathy indicates favourable outcome and inflammation control.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1134, doi. 10.1093/eurheartj/ehq498
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Arrhythmogenic right ventricular cardiomyopathy/dysplasia on the basis of the revised diagnostic criteria in affected families with desmosomal mutations.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1097, doi. 10.1093/eurheartj/ehr043
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A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1065, doi. 10.1093/eurheartj/ehr105
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Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1121, doi. 10.1093/eurheartj/ehq507
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‘Iron deficiency: an ominous sign in patients with systolic chronic heart failure’ [Eur Heart J 2010;31:1872–1880, doi:10.1093/eurheartj/ehq158].
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- European Heart Journal, 2011, v. 32, n. 9, p. 1054, doi. 10.1093/eurheartj/ehr115
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Right ventricular obstruction by metastatic malignant mixed Müllerian tumour.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1171, doi. 10.1093/eurheartj/ehq460
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Left bundle branch block during pregnancy as a sign of imminent peripartum cardiomyopathy.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1076, doi. 10.1093/eurheartj/ehq487
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Prevalence and clinical correlates of QT prolongation in patients with hypertrophic cardiomyopathy.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1114, doi. 10.1093/eurheartj/ehr021
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To kill two birds with one stone: a pleurocentesis that also drained pericardial tamponade in a stubbed patient.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1147, doi. 10.1093/eurheartj/ehq462
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Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1161, doi. 10.1093/eurheartj/ehr092
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Corrigendum to: ‘Guidelines for the management of atrial fibrillation’ [European Heart Journal (2010) 31, 2369–2429 and EP-Europace (2010) 12, 1360–1420].
- Published in:
- European Heart Journal, 2011, v. 32, n. 9, p. 1172, doi. 10.1093/eurheartj/ehq512
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The Holy Grail of LVAD-induced reversal of severe chronic heart failure: the need for integration.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1052, doi. 10.1093/eurheartj/ehq503
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The multiple facets of right ventricular cardiomyopathies.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1049, doi. 10.1093/eurheartj/ehr088
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Hypertrophic obstructive cardiomyopathy: alcohol septal ablation.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1059, doi. 10.1093/eurheartj/ehr013
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Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6).
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- European Heart Journal, 2011, v. 32, n. 9, p. 1077, doi. 10.1093/eurheartj/ehr076
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Heart failure reversal by ventricular unloading in patients with chronic cardiomyopathy: criteria for weaning from ventricular assist devices.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1148, doi. 10.1093/eurheartj/ehq353
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Right ventricular mechanical dispersion is related to malignant arrhythmias: a study of patients with arrhythmogenic right ventricular cardiomyopathy and subclinical right ventricular dysfunction.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1089, doi. 10.1093/eurheartj/ehr069
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Prognostic predictors in arrhythmogenic right ventricular cardiomyopathy: results from a 10-year registry.
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- European Heart Journal, 2011, v. 32, n. 9, p. 1105, doi. 10.1093/eurheartj/ehr040
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