Xenética Cardiovascular
Complexo Hospitalario Universitario de Santiago
Santiago de Compostela, EspañaPublicacións en colaboración con investigadores/as de Complexo Hospitalario Universitario de Santiago (50)
2024
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Correction in article by Juzga-Corrales et al. “Characteristics and outcomes of the Spanish registry for pediatric patients with bicuspid aortic valve (REVAB)”, Rev Esp Cardiol. 2023;76:961-969 (Revista Española de Cardiología (English Edition) (2024) 77(4) (358–359), (S1885585724000331), (10.1016/j.rec.2023.12.011))
Revista Espanola de Cardiologia
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Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives
Journal of the American College of Cardiology, Vol. 83, Núm. 17, pp. 1640-1651
2023
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Characteristics and outcomes of the Spanish registry for pediatric patients with bicuspid aortic valve (REVAB)
Revista Espanola de Cardiologia, Vol. 76, Núm. 12, pp. 961-969
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Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel Sequencing
Molecular Diagnosis and Therapy, Vol. 27, Núm. 1, pp. 105-113
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Late gadolinium enhancement distribution patterns in non-ischaemic dilated cardiomyopathy: genotype-phenotype correlation
European heart journal. Cardiovascular Imaging, Vol. 25, Núm. 1, pp. 75-85
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Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death
Frontiers in Medicine, Vol. 10
2022
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Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy
Journal of the American College of Cardiology, Vol. 80, Núm. 12, pp. 1115-1126
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Combination of late gadolinium enhancement and genotype improves prediction of prognosis in non-ischaemic dilated cardiomyopathy
European Journal of Heart Failure, Vol. 24, Núm. 7, pp. 1183-1196
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
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Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome
PLoS ONE, Vol. 17, Núm. 3 March
2021
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Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy
Journal of the American College of Cardiology, Vol. 78, Núm. 17, pp. 1682-1699
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Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy
Forensic Science International: Genetics, Vol. 52
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Gaucher disease
Revista Colombiana de Cardiologia, Vol. 28, pp. 30-40
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Molecular study of sticky platelet syndrome using exome sequencing
Revista Facultad de Medicina, Vol. 69, Núm. 3
2020
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The place of metropolitan France in the European genomic landscape
Human Genetics, Vol. 139, Núm. 8, pp. 1091-1105
2019
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A Novel Calsequestrin 2 Deletion Causing Catecholaminergic Polymorphic Ventricular Tachycardia and Sudden Cardiac Death
Revista Espanola de Cardiologia, Vol. 72, Núm. 8, pp. 681-683
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Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths
Forensic Science International: Genetics, Vol. 42, pp. 203-212
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Mobile thrombus in right atrium during cannulation of veno-venous extracorporeal membrane oxygenation
Medicina Intensiva, Vol. 43, Núm. 6, pp. 390-391
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Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation
Forensic Science International: Genetics, Vol. 43
2018
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Innovative Strategies in Heart Failure: Present and Future
Archives of Medical Research, Vol. 49, Núm. 8, pp. 558-567