Susceptibility to innate immune activation in genetically mediated myocarditis
DF Selgrade, DE Fullenkamp, IA Chychula, B Li… - The Journal of Clinical …, 2024 - jci.org
Myocarditis is clinically characterized by chest pain, arrhythmias, and heart failure, and
treatment is often supportive. Mutations in DSP, a gene encoding the desmosomal protein …
treatment is often supportive. Mutations in DSP, a gene encoding the desmosomal protein …
DSP-Related Cardiomyopathy as a Distinct Clinical Entity? Emerging Evidence from an Italian Cohort
F Di Lorenzo, E Marchionni, V Ferradini… - International Journal of …, 2023 - mdpi.com
Variants in desmoplakin gene (DSP MIM* 125647) have been usually associated with
Arrhythmogenic Cardiomyopathy (ACM), or Dilated Cardiomyopathy (DCM) inherited in an …
Arrhythmogenic Cardiomyopathy (ACM), or Dilated Cardiomyopathy (DCM) inherited in an …
Proteomic analysis of lung responses to SARS-CoV-2 infection in aged non-human primates: clinical and research relevance
A Garcia-Vilanova, A Allué-Guardia, NM Chacon… - GeroScience, 2024 - Springer
With devastating health and socioeconomic impact worldwide, much work is left to
understand the Coronavirus Disease 2019 (COVID-19), with emphasis in the severely …
understand the Coronavirus Disease 2019 (COVID-19), with emphasis in the severely …
Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac death
Objective We conducted an investigation into the clinical and molecular characteristics of
Arrhythmogenic left ventricular cardiomyopathy (ALVC) caused by a novel likely pathogenic …
Arrhythmogenic left ventricular cardiomyopathy (ALVC) caused by a novel likely pathogenic …
Cardiac Inflammation in Adult-Onset Genetic Dilated Cardiomyopathy
MA Sikking, SLVM Stroeks, MTHM Henkens… - Journal of Clinical …, 2023 - mdpi.com
Dilated cardiomyopathy (DCM) has a genetic cause in up to 40% of cases, with differences
in disease penetrance and clinical presentation, due to different exogeneous triggers and …
in disease penetrance and clinical presentation, due to different exogeneous triggers and …
[HTML][HTML] The role of genetic testing in suspected fulminant myocarditis: A case report
R Mistrulli, C Micolonghi, F Follesa, M Fabiani… - Molecular Genetics and …, 2023 - Elsevier
ACM is a rare hereditary heart disease characterized by a progressive fibro-fatty
replacement of the myocardium that can affect either the right or the left ventricle or both. It is …
replacement of the myocardium that can affect either the right or the left ventricle or both. It is …
[HTML][HTML] Десмоплакин и особенности течения десмоплакиновой кардиомиопатии
РП Мясников, НН Кузина, ДА Нефедова… - Российский …, 2023 - cyberleninka.ru
Наследственные кардиомиопатии (КМП)—это группа гетерогенных заболеваний,
характеризующихся патологией сердечной мышцы, не обусловленной ишемической …
характеризующихся патологией сердечной мышцы, не обусловленной ишемической …
Desmoplakin and features of desmoplakin cardiomyopathy
RP Myasnikov, NN Kuzina… - Russian Journal of …, 2023 - russjcardiol.elpub.ru
Inherited cardiomyopathies (CMP) are a group of heterogeneous diseases characterized by
myocardial disorders that is not caused by coronary artery disease, hypertension, valvular …
myocardial disorders that is not caused by coronary artery disease, hypertension, valvular …