JUAN JIMÉNEZ JÁIMEZ-rekin lankidetzan egindako argitalpenak (4)

2023

  1. 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

2021

  1. Heterozygous arrhythmogenic cardiomyopathy-desmoplakin mutation carriers exhibit a subclinical cutaneous phenotype with cell membrane disruption and lack of intercellular adhesion

    Journal of Clinical Medicine, Vol. 10, Núm. 19

2020

  1. Myocardial fibrosis in arrhythmogenic cardiomyopathy: A genotype-phenotype correlation study

    European Heart Journal Cardiovascular Imaging, Vol. 21, Núm. 4, pp. 378-386

2018

  1. Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia

    Circulation, Vol. 137, Núm. 15, pp. 1595-1610