Bases Moleculares de la Arteriosclerosis
CTS347
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Universitat de Barcelona
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Universitat de Barcelona (17)
2024
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A narrative review of inherited arrhythmogenic syndromes in young population: Role of genetic diagnosis in exercise recommendations
BMJ Open Sport and Exercise Medicine, Vol. 10, Núm. 3
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Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy
International Journal of Molecular Sciences, Vol. 25, Núm. 7
2023
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Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort
International Journal of Legal Medicine, Vol. 137, Núm. 2, pp. 345-351
2022
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Clinical impact of rare variants associated with inherited channelopathies: a 5-year update
Human Genetics, Vol. 141, Núm. 10, pp. 1579-1589
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Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes
Journal of Personalized Medicine, Vol. 12, Núm. 2
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The Role of MicroRNAs in Dilated Cardiomyopathy: New Insights for an Old Entity
International Journal of Molecular Sciences, Vol. 23, Núm. 21
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miR-16-5p Suppression Protects Human Cardiomyocytes against Endoplasmic Reticulum and Oxidative Stress-Induced Injury
International Journal of Molecular Sciences, Vol. 23, Núm. 3
2021
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Malignant arrhythmogenic role associated with rbm20: A comprehensive interpretation focused on a personalized approach
Journal of Personalized Medicine, Vol. 11, Núm. 2, pp. 1-17
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Personalized genetic diagnosis of congenital heart defects in newborns
Journal of Personalized Medicine, Vol. 11, Núm. 6
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Rare variants associated with arrhythmogenic cardiomyopathy: Reclassification five years later
Journal of Personalized Medicine, Vol. 11, Núm. 3, pp. 1-14
2020
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Genetic variants as sudden-death risk markers in inherited arrhythmogenic syndromes: Personalized genetic interpretation
Journal of Clinical Medicine, Vol. 9, Núm. 6, pp. 1-9
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Peripheral microRNA panels to guide the diagnosis of familial cardiomyopathy
Translational Research, Vol. 218, pp. 1-15
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Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes
EBioMedicine, Vol. 54
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Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
Forensic Science International: Genetics, Vol. 47
2016
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Genetic basis of dilated cardiomyopathy
International Journal of Cardiology, Vol. 224, pp. 461-472
2015
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A novel mutation in lamin A/C causing familial dilated cardiomyopathy associated with sudden cardiac death
Journal of Cardiac Failure, Vol. 21, Núm. 3, pp. 217-225
2009
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Thigh and buttock exertional pain for the diagnosis of peripheral arterial disease
European Journal of Internal Medicine, Vol. 20, Núm. 4, pp. 429-434