JUAN
JIMÉNEZ JÁIMEZ
PROFESOR CONTRATADO DOCTOR
Publications (110) JUAN JIMÉNEZ JÁIMEZ publications
2024
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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
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Atypical left-ventricular hypertrophy with apical aneurysm in leopard syndrome
International Journal of Cardiovascular Imaging, Vol. 40, Núm. 8, pp. 1809-1811
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Extracellular Kir2.1C122Y Mutant Upsets Kir2.1-PIP2Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome
Circulation Research, Vol. 134, Núm. 8, pp. E52-E71
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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
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Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy
JACC: Clinical Electrophysiology, Vol. 10, Núm. 6, pp. 1178-1190
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Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus report
International Journal of Cardiology, Vol. 395
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Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction
Circulation: Genomic and Precision Medicine, Vol. 17, Núm. 2, pp. E004404
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Usefulness of genetic study in early onset atrial fibrillation
REC: CardioClinics
2023
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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
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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
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Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
European heart journal, Vol. 44, Núm. 35, pp. 3357-3370
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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
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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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Lifestyle physical activity and rapid-rate non-sustained ventricular tachycardia in arrhythmogenic cardiomyopathy
Heart, Vol. 109, Núm. 13, pp. 992-999
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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
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Selection of the best of 2022 in familial heart disease and cardiovascular genetics
REC: CardioClinics, Vol. 58, pp. S68-S73
2022
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Antiarrhythmic effect of sacubitril/valsartan in high arrhythmic risk inherited cardiomyopathies
REC: CardioClinics, Vol. 57, Núm. 3, pp. 219-221
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Characterization of hereditary transthyretin cardiac amyloidosis in Spain
Revista Espanola de Cardiologia, Vol. 75, Núm. 6, pp. 488-495
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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
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Effect of programmed electrical cardioversion of atrial fibrillation on renal function
Revista Colombiana de Cardiologia, Vol. 29, Núm. 3, pp. 286-294