Publications (117) JUAN JIMÉNEZ JÁIMEZ publications

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2025

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

    International Journal of Cardiology, Vol. 418

  2. Left bundle branch area pacing in a case of Steinert's disease

    HeartRhythm Case Reports, Vol. 11, Núm. 4, pp. 318-321

  3. Left ventricular ejection fraction decline and cardiovascular events in suspected cardiomyopathy with excessive trabeculation: toward precision medicine

    Revista Espanola de Cardiologia

  4. Successful ablation of Purkinje-related ventricular ectopy leading to ventricular fibrillation in Emery-Dreifuss dilated cardiomyopathy

    Journal of Interventional Cardiac Electrophysiology

  5. Usefulness of genetic study in early onset atrial fibrillation

    REC: CardioClinics, Vol. 60, Núm. 1, pp. 61-64

  6. Vector field heterogeneity as a novel omnipolar mapping metric for functional substrate characterization in scar-related ventricular tachycardias

    Heart Rhythm, Vol. 22, Núm. 5, pp. 1218-1228

  7. Wide QRS Tachycardia With VA Dissociation: What Is the Mechanism?

    Journal of Cardiovascular Electrophysiology

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. Electrophysiological Phenotype-Genotype Study of Sustained Monomorphic Ventricular Tachycardia in Inherited, High Arrhythmic Risk, Left Ventricular Cardiomyopathy

    Circulation: Arrhythmia and Electrophysiology, Vol. 17, Núm. 12, pp. e013145

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

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

  5. Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives

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

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

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

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

    International Journal of Cardiology, Vol. 395

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

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

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