Juan Jiménez-Jáimez

TL;DR: In this article, the authors demonstrate the association between truncating mutations in the Filamin C (FLNC) gene and the development of high-risk dilated and arrhythmogenic cardiomyopathies.

TL;DR: Calmodulinopathies are largely characterized by adrenergically-induced life-threatening arrhythmias, and available therapies are disquietingly insufficient, especially in CALM-LQTS.

TL;DR: SLE with MS presented higher levels of inflammatory markers than SLE without MS and educational level, serum triglycerides, HDL-cholesterol and C3 serum levels and hydroxychloroquine use were independently associated with MS.

TL;DR: DCM caused by mutations in BAG3 is characterized by high penetrance in carriers >40 years of age and a high risk of progressive heart failure.

TL;DR: The novel DES-p.Glu401Asp mutation causes predominant inherited left ventricular arrhythmogenic cardiomyopathy/dysplasia with a high incidence of adverse clinical events in the absence of skeletal myopathy or conduction system disorders.