Precision Medicine and Cardiac Channelopathies: Human iPSCs Take the Lead

SA Sebastian, V Panthangi, Y Sethi, I Padda… - Current problems in …, 2023 - Elsevier
Sudden cardiac death (SCD) is one of the leading causes of death worldwide, usually
involving young people. SCD remains a critical public health problem accounting for …

Disease‐modifying therapies for amyloid transthyretin cardiomyopathy: Current and emerging medications

EL Hellenbart, HJ Ipema… - … : The Journal of …, 2024 - Wiley Online Library
Transthyretin amyloidosis (ATTR) is a rare disease that results in amyloid fibril misfolding
and deposition in multiple organs, including the heart, leading to the development of ATTR …

[HTML][HTML] Cardiac amyloidosis: evolving pathogenesis, multimodal diagnostics, and principles of treatment

GD Medarametla, RS Kahlon, L Mahitha, S Shariff… - EXCLI …, 2023 - ncbi.nlm.nih.gov
Amyloidosis is a protein deposition disorder in which insoluble fibril structures accumulate in
the bodily tissues damaging the organ function. Cardiac amyloidosis is a severe but under …

Arrhythmogenic Left Ventricular Cardiomyopathy: From Diagnosis to Risk Management

A Mauriello, AS Roma, A Ascrizzi, R Molinari… - Journal of Clinical …, 2024 - mdpi.com
Purpose of Review: Left ventricular arrhythmogenic cardiomyopathy (ALVC) is a rare and
poorly characterized cardiomyopathy that has recently been reclassified in the group of non …

Genetics of the Cardiomyopathies: A Review for the Cardiologist

FL Scolari, HI Garbin, TMA Beuren… - ABC Heart Fail …, 2024 - abcheartfailure.org
Cardiomyopathies, myocardial diseases without other causative factors like hypertension or
coronary artery disease, were once considered rare but have seen increased diagnoses …