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Corrigendum to: Arrhythmogenic cardiomyopathy presenting as an inflammatory cardiomyopathy: the role of <sup>18</sup>F-fluorodeoxyglucose positron emission tomography scan.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2021, v. 22, n. 8, p. e136, doi. 10.1093/ehjci/jeab125
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- Article
Arrhythmogenic cardiomyopathy presenting as an inflammatory cardiomyopathy: the role of <sup>18</sup>F-fluorodeoxyglucose positron emission tomography scan.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2021, v. 22, n. 8, p. e126, doi. 10.1093/ehjci/jeab066
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- Publication type:
- Article
Arrhythmic risk prediction in arrhythmogenic right ventricular cardiomyopathy: external validation of the arrhythmogenic right ventricular cardiomyopathy risk calculator.
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- European Heart Journal, 2022, v. 43, n. 32, p. 3041, doi. 10.1093/eurheartj/ehac289
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- Article
β3 adrenergic agonist treatment in chronic pulmonary hypertension associated with heart failure (SPHERE‐HF): a double blind, placebo‐controlled, randomized clinical trial.
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- European Journal of Heart Failure, 2023, v. 25, n. 3, p. 373, doi. 10.1002/ejhf.2745
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- Article
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update.
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- Human Genetics, 2022, v. 141, n. 10, p. 1579, doi. 10.1007/s00439-021-02370-4
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- Article
Hypertrophic cardiomyopathy: Sudden cardiac death risk stratification in adults.
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- Global Cardiology Science & Practice, 2018, v. 2018, n. 3, p. 1, doi. 10.21542/gcsp.2018.25
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- Article
Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.
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- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00450
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- Article
Outcomes of Septal Myectomy beyond 65 Years, with and without Concomitant Procedures †.
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- Journal of Clinical Medicine, 2021, v. 10, n. 16, p. 3499, doi. 10.3390/jcm10163499
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- Article
Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation.
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- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1866, doi. 10.3390/jcm9061866
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- Article
Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants.
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- Journal of Clinical Medicine, 2019, v. 8, n. 10, p. 1035, doi. 10.3390/jcm8071035
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- Article
Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants.
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- Journal of Clinical Medicine, 2019, v. 8, n. 7, p. 1035, doi. 10.3390/jcm8071035
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- Article
Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later.
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- Journal of Personalized Medicine, 2021, v. 11, n. 3, p. 162, doi. 10.3390/jpm11030162
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- Article
Malignant Arrhythmogenic Role Associated with RBM20 : A Comprehensive Interpretation Focused on a Personalized Approach.
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- Journal of Personalized Medicine, 2021, v. 11, n. 2, p. 130, doi. 10.3390/jpm11020130
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- Article