Francisco J Bermudez-Jimenez
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Explore the profile of Francisco J Bermudez-Jimenez including associated specialties, affiliations and a list of published articles.
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11
Citations
43
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Recent Articles
1.
Cruz F, Moreno-Manuel A, Perez P, Ruiz-Robles J, Socuellamos P, Gutierrez L, et al.
medRxiv
. 2024 Dec;
PMID: 39711719
Background: Flecainide and other class-Ic antiarrhythmic drugs (AADs) are widely used in Andersen-Tawil syndrome type 1 (ATS1) patients. However, class-Ic drugs might be proarrhythmic in some cases. We investigated the...
2.
Cabrera-Borrego E, Bermudez-Jimenez F, Gasperetti A, Tandri H, Sanchez-Millan P, Molina-Lerma M, et al.
Circ Arrhythm Electrophysiol
. 2024 Nov;
17(12):e013145.
PMID: 39611258
Background: Among inherited cardiomyopathies involving the left ventricle, whether dilated or not, certain genotypes carry a well-established arrhythmic risk, notably manifested as sustained monomorphic ventricular tachycardia (SMVT). Nonetheless, the precise...
3.
Bermudez-Jimenez F, Protonotarios A, Garcia-Hernandez S, Perez Asensio A, Rampazzo A, Zorio E, et al.
JACC Clin Electrophysiol
. 2024 May;
10(6):1178-1190.
PMID: 38727660
Background: Desmin (DES) pathogenic variants cause a small proportion of arrhythmogenic cardiomyopathy (ACM). Outcomes data on DES-related ACM are scarce. Objectives: This study sought to provide information on the clinical...
4.
Extracellular Kir2.1 Mutant Upsets Kir2.1-PIP Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome
Cruz F, Macias A, Moreno-Manuel A, Gutierrez L, Vera-Pedrosa M, Martinez-Carrascoso I, et al.
Circ Res
. 2024 Mar;
134(8):e52-e71.
PMID: 38497220
Background: Andersen-Tawil syndrome type 1 is a rare heritable disease caused by mutations in the gene coding the strong inwardly rectifying K channel Kir2.1. The extracellular Cys (cysteine)-to-Cys disulfide bond...
5.
Cruz F, Macias A, Moreno-Manuel A, Gutierrez L, Vera-Pedrosa M, Martinez-Carrascoso I, et al.
bioRxiv
. 2023 Jun;
PMID: 37333254
Background: Andersen-Tawil Syndrome Type 1 (ATS1) is a rare heritable disease caused by mutations in the strong inwardly rectifying K channel Kir2.1. The extracellular Cys122-to-Cys154 disulfide bond in the Kir2.1...
6.
Laredo M, Tovia-Brodie O, Milman A, Michowitz Y, Roudijk R, Peretto G, et al.
Europace
. 2023 Jan;
25(3):1025-1034.
PMID: 36635857
Aims: Little is known about patients with right bundle branch block (RBBB)-ventricular tachycardia (VT) and arrhythmogenic cardiomyopathy (ACM). Our aims were: (i) to describe electrocardiogram (ECG) characteristics of sinus rhythm...
7.
Escobar-Lopez L, Ochoa J, Royuela A, Verdonschot J, Dal Ferro M, Espinosa M, et al.
J Am Coll Cardiol
. 2022 Sep;
80(12):1115-1126.
PMID: 36109106
Background: Although genotyping allows family screening and influences risk-stratification in patients with nonischemic dilated cardiomyopathy (DCM) or isolated left ventricular systolic dysfunction (LVSD), its result is negative in a significant...
8.
Belhassen B, Laredo M, Roudijk R, Peretto G, Zahavi G, Sen-Chowdhry S, et al.
Europace
. 2021 Sep;
24(2):285-295.
PMID: 34491328
Aims: In arrhythmogenic cardiomyopathy (ACM), sustained ventricular tachycardia (VT) typically displays a left bundle branch block (LBBB) morphology while a right bundle branch block (RBBB) morphology is rare. The present...
9.
Barriales-Villa R, Ochoa J, Larranaga-Moreira J, Salazar-Mendiguchia J, Diez-Lopez C, Restrepo-Cordoba M, et al.
Rev Esp Cardiol (Engl Ed)
. 2020 Jul;
74(3):216-224.
PMID: 32616434
Introduction And Objectives: According to sudden cardiac death guidelines, an implantable cardioverter-defibrillator (ICD) should be considered in patients with LMNA-related dilated cardiomyopathy (DCM) and ≥ 2 risk factors: male sex,...
10.
Bermudez-Jimenez F, Jimenez-Jaimez J
J Am Coll Cardiol
. 2018 Jun;
71(24):2864.
PMID: 29903360
No abstract available.