Found: 30
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Long-term reliability of the phospholamban (PLN) p.(Arg14del) risk model in predicting major ventricular arrhythmia: a landmark study.
- Published in:
- EP: Europace, 2024, v. 26, n. 4, p. 1, doi. 10.1093/europace/euae069
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- Publication type:
- Article
Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype.
- Published in:
- EP: Europace, 2014, v. 16, n. 12, p. 1838, doi. 10.1093/europace/euu128
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- Publication type:
- Article
Polymorphisms in ACE, ACE2, AGTR1 genes and severity of COVID-19 disease.
- Published in:
- PLoS ONE, 2022, v. 17, n. 2, p. 1, doi. 10.1371/journal.pone.0263140
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- Publication type:
- Article
Lamin A/C Ablation Restricted to Vascular Smooth Muscle Cells, Cardiomyocytes, and Cardiac Fibroblasts Causes Cardiac and Vascular Dysfunction.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 13, p. 11172, doi. 10.3390/ijms241311172
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- Publication type:
- Article
Atypical Cause of Syncope in Patients with Brugada Syndrome.
- Published in:
- European Journal of Cardiovascular Medicine, 2013, v. 2, n. 3, p. 160, doi. 10.5083/ejcm.20424884.91
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- Publication type:
- Article
Genetics of feline hypertrophic cardiomyopathy.
- Published in:
- Clinical Genetics, 2020, v. 98, n. 3, p. 203, doi. 10.1111/cge.13743
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- Publication type:
- Article
Endomyocardial biopsy: safety and prognostic utility in paediatric and adult myocarditis in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Long-Term Registry.
- Published in:
- European Heart Journal, 2024, v. 45, n. 28, p. 2548, doi. 10.1093/eurheartj/ehae169
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- Publication type:
- Article
2023 ESC Guidelines for the management of cardiomyopathies: Developed by the task force on the management of cardiomyopathies of the European Society of Cardiology (ESC).
- Published in:
- European Heart Journal, 2023, v. 44, n. 37, p. 3503, doi. 10.1093/eurheartj/ehad194
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- Publication type:
- Article
An expert consensus document on the management of cardiovascular manifestations of Fabry disease.
- Published in:
- 2020
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- Publication type:
- journal article
Left ventricular outflow tract obstruction and sudden death risk in patients with hypertrophic cardiomyopathy.
- Published in:
- European Heart Journal, 2006, v. 27, n. 16, p. 1933, doi. 10.1093/eurheartj/ehl041
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- Publication type:
- Article
Current therapies for hypertrophic cardiomyopathy: a systematic review and meta‐analysis of the literature.
- Published in:
- ESC Heart Failure, 2023, v. 10, n. 1, p. 8, doi. 10.1002/ehf2.14142
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- Publication type:
- Article
Impact of SARS‐Cov‐2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry.
- Published in:
- ESC Heart Failure, 2022, v. 9, n. 4, p. 2189, doi. 10.1002/ehf2.13964
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- Publication type:
- Article
Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry.
- Published in:
- ESC Heart Failure, 2021, v. 8, n. 1, p. 95, doi. 10.1002/ehf2.13100
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- Publication type:
- Article
Atrial fibrillation, anticoagulation management and risk of stroke in the Cardiomyopathy/Myocarditis registry of the EURObservational Research Programme of the European Society of Cardiology.
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- ESC Heart Failure, 2020, v. 7, n. 6, p. 3601, doi. 10.1002/ehf2.12854
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- Publication type:
- Article
ESC EORP Cardiomyopathy Registry: real‐life practice of genetic counselling and testing in adult cardiomyopathy patients.
- Published in:
- ESC Heart Failure, 2020, v. 7, n. 5, p. 3013, doi. 10.1002/ehf2.12925
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- Publication type:
- Article
Percutaneous coronary intervention with rotational atherectomy for severely calcified unprotected left main: Immediate and two-years follow-up results.
- Published in:
- Catheterization & Cardiovascular Interventions, 2012, v. 80, n. 2, p. 215, doi. 10.1002/ccd.23419
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- Publication type:
- Article
Alcohol septal ablation in hypertrophic cardiomyopathy.
- Published in:
- Global Cardiology Science & Practice, 2018, v. 2018, n. 3, p. 1, doi. 10.21542/gcsp.2018.30
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- Publication type:
- Article
A new KCNQ1 mutation at the S5 segment that impairs its association with KCNE1 is responsible for short QT syndrome.
- Published in:
- Cardiovascular Research, 2015, v. 107, n. 4, p. 613, doi. 10.1093/cvr/cvv196
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- Publication type:
- Article
Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy.
- Published in:
- Nature Medicine, 2013, v. 19, n. 2, p. 193, doi. 10.1038/nm.3046
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- Publication type:
- Article
Towards an Enhanced Tool for Quantifying the Degree of LV Hyper-Trabeculation.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 3, p. 503, doi. 10.3390/jcm10030503
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- Publication type:
- Article
Genetic Factors Involved in Cardiomyopathies and in Cancer.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1702, doi. 10.3390/jcm9061702
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- Publication type:
- Article
Prediction of ventricular arrhythmia in phospholamban p.Arg14del mutation carriers–reaching the frontiers of individual risk prediction.
- Published in:
- European Heart Journal, 2021, v. 49, n. 29, p. 2842, doi. 10.1093/eurheartj/ehab294
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- Publication type:
- Article
The Cardiomyopathy Registry of the EURObservational Research Programme of the European Society of Cardiology: baseline data and contemporary management of adult patients with cardiomyopathies.
- Published in:
- European Heart Journal, 2018, v. 39, n. 20, p. 1784, doi. 10.1093/eurheartj/ehx819
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- Publication type:
- Article
ALG12‐CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1304
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- Publication type:
- Article
Estratificación del riesgo en la muerte súbita por miocardiopatía hipertrófica.
- Published in:
- CorSalud, 2017, v. 9, n. 3, p. 218
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- Publication type:
- Article
Impacto del protocolo multidisciplinar de muerte súbita en la región de Murcia (España).
- Published in:
- CorSalud, 2017, v. 9, n. 3, p. 185
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- Publication type:
- Article
An R1632C variant in the SCN5A gene causing Brugada syndrome.
- Published in:
- 2016
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- Publication type:
- Case Study
The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the European Society of Human Genetics
- Published in:
- European Heart Journal, 2015, v. 36, n. 22, p. 1367, doi. 10.1093/eurheartj/ehv122
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- Publication type:
- Article
Exercise-induced ventricular arrhythmias and risk of sudden cardiac death in patients with hypertrophic cardiomyopathy.
- Published in:
- European Heart Journal, 2009, v. 30, n. 21, p. 2599, doi. 10.1093/eurheartj/ehp327
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- Publication type:
- Article
EP300/TP53 pathway, a suppressor of the Hippo and canonical WNT pathways, is activated in human hearts with arrhythmogenic cardiomyopathy in the absence of overt heart failure.
- Published in:
- Cardiovascular Research, 2022, v. 118, n. 6, p. 1466, doi. 10.1093/cvr/cvab197
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- Publication type:
- Article