Argitalpenak (111) JUAN JIMÉNEZ JÁIMEZ argitalpenak

2025

  1. Late gadolinium enhancement and outcome of cardiac resynchronization therapy in non-ischemic cardiomyopathy

    International Journal of Cardiology, Vol. 418

2024

  1. A rare presentation of infective endocarditis: Phase 4 block of the left bundle branch as key for the diagnosis. A case report

    Journal of Electrocardiology, Vol. 85, pp. 72-74

  2. Atypical left-ventricular hypertrophy with apical aneurysm in leopard syndrome

    International Journal of Cardiovascular Imaging, Vol. 40, Núm. 8, pp. 1809-1811

  3. Extracellular Kir2.1C122Y Mutant Upsets Kir2.1-PIP2Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome

    Circulation Research, Vol. 134, Núm. 8, pp. E52-E71

  4. Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives

    Journal of the American College of Cardiology, Vol. 83, Núm. 17, pp. 1640-1651

  5. Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy

    JACC: Clinical Electrophysiology, Vol. 10, Núm. 6, pp. 1178-1190

  6. Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus report

    International Journal of Cardiology, Vol. 395

  7. Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction

    Circulation: Genomic and Precision Medicine, Vol. 17, Núm. 2, pp. E004404

  8. Usefulness of genetic study in early onset atrial fibrillation

    REC: CardioClinics

2023

  1. A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 120

  2. Autothreshold algorithm feasibility and safety in left bundle branch pacing

    Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, Vol. 26, Núm. 1

  3. Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

    European heart journal, Vol. 44, Núm. 35, pp. 3357-3370

  4. Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure

    European Heart Journal, Vol. 44, Núm. 48, pp. 5064-5073

  5. 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

  6. Lifestyle physical activity and rapid-rate non-sustained ventricular tachycardia in arrhythmogenic cardiomyopathy

    Heart, Vol. 109, Núm. 13, pp. 992-999

  7. ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardium

    Revista Espanola de Cardiologia, Vol. 76, Núm. 5, pp. 301-311

  8. Selection of the best of 2022 in familial heart disease and cardiovascular genetics

    REC: CardioClinics, Vol. 58, pp. S68-S73

2022

  1. Antiarrhythmic effect of sacubitril/valsartan in high arrhythmic risk inherited cardiomyopathies

    REC: CardioClinics, Vol. 57, Núm. 3, pp. 219-221

  2. Characterization of hereditary transthyretin cardiac amyloidosis in Spain

    Revista Espanola de Cardiologia, Vol. 75, Núm. 6, pp. 488-495

  3. Dinámica del miocardio. Mecanismos de reserva de la función ventricular. Mecanismos compensadores en la insuficiencia cardiaca. Remodelado ventricular. Manifestaciones clínicas de la insuficiencia cardiaca

    Bases de la medicina interna. Fisiopatología y propedéutica médica: Volumen II (Avicam), pp. 25-46