[HTML][HTML] Update on the diagnostic pitfalls of autopsy and post-mortem genetic testing in cardiomyopathies
S Grassi, O Campuzano, M Coll, F Cazzato… - International Journal of …, 2021 - mdpi.com
Inherited cardiomyopathies are frequent causes of sudden cardiac death (SCD), especially
in young patients. Despite at the autopsy they usually have distinctive microscopic and/or …
in young patients. Despite at the autopsy they usually have distinctive microscopic and/or …
[HTML][HTML] Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era
P Teekakirikul, MA Kelly, HL Rehm… - The Journal of Molecular …, 2013 - Elsevier
Inherited cardiomyopathies include hypertrophic cardiomyopathy, dilated cardiomyopathy,
arrhythmogenic right ventricular cardiomyopathy, left ventricular noncompaction, and …
arrhythmogenic right ventricular cardiomyopathy, left ventricular noncompaction, and …
Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all
Cardiomyopathies are an important and heterogeneous group of common cardiac diseases.
An increasing number of cardiomyopathies are now recognized to have familial forms, which …
An increasing number of cardiomyopathies are now recognized to have familial forms, which …
[HTML][HTML] The role of genetic testing in the identification of young athletes with inherited primitive cardiac disorders at risk of exercise sudden death
FD Tiziano, V Palmieri, M Genuardi… - Frontiers in …, 2016 - frontiersin.org
Although relatively rare, inherited primitive cardiac disorders (IPCDs) in athletes have a
deep social impact since they often present as sudden cardiac death (SCD) of young and …
deep social impact since they often present as sudden cardiac death (SCD) of young and …
Genetic testing as a guide for treatment in dilated cardiomyopathies
S Garcia-Hernandez, LM Iglesias - Current Cardiology Reports, 2022 - Springer
Abstract Purpose of Review Dilated cardiomyopathy (DCM) is one of the most prevalent
primary cardiomyopathies and may be caused by genetic and non-genetic etiologies. DCM …
primary cardiomyopathies and may be caused by genetic and non-genetic etiologies. DCM …
[HTML][HTML] Accurate classification of non-ischemic cardiomyopathy
Y Wang, H Jia, J Song - Current Cardiology Reports, 2023 - Springer
Abstractt Purpose of Review This article aims to review the accurate classification of non-
ischemic cardiomyopathy, including the methods, basis, subtype characteristics, and …
ischemic cardiomyopathy, including the methods, basis, subtype characteristics, and …
[HTML][HTML] Morphological and genetic aspects for Post-mortem diagnosis of hypertrophic cardiomyopathy: a systematic review
V Cianci, E Forzese, D Sapienza, L Cardia… - International Journal of …, 2024 - mdpi.com
Hypertrophic cardiomyopathy (HCM) is one of the most common genetic cardiovascular
diseases, and it shows an autosomal dominant pattern of inheritance. HCM can be clinically …
diseases, and it shows an autosomal dominant pattern of inheritance. HCM can be clinically …
Multidisciplinary approach in cardiomyopathies: From genetics to advanced imaging
F Santoro, E Vitale, I Ragnatela, R Cetera… - Heart Failure …, 2024 - Springer
Cardiomyopathies are myocardial diseases characterized by mechanical and electrical
dysfunction of the heart muscle which could lead to heart failure and life-threatening …
dysfunction of the heart muscle which could lead to heart failure and life-threatening …
[HTML][HTML] Genetically determined cardiomyopathies at autopsy: the pivotal role of the pathologist in establishing the diagnosis and guiding family screening
Cardiomyopathies (CMP) comprise a heterogenous group of diseases affecting primarily the
myocardium, either genetic and/or acquired in origin. While many classification systems …
myocardium, either genetic and/or acquired in origin. While many classification systems …
Evolving approaches to genetic evaluation of specific cardiomyopathies
LYL Teo, RT Moran, WHW Tang - Current heart failure reports, 2015 - Springer
The understanding of the genetic basis of cardiomyopathy has expanded significantly over
the past 2 decades. The increasing availability, shortening diagnostic time, and lowering …
the past 2 decades. The increasing availability, shortening diagnostic time, and lowering …