Familial Dilated Cardiomyopathy Latest Advances

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: August 08, 2025

CRYAB Missense Mutation Reveals Shared Pathogenesis of Familial Cardiomyopathy and Arrhythmia.

Journal: Genes

Published: August 04, 2025

Early Detection of Subclinical Myocardial Dysfunction in Familial Dilated Cardiomyopathy Using Myocardial Work Analysis.

Journal: Diagnostics (Basel, Switzerland)

Published: August 01, 2025

Investigation into the relationship between the etiology of dilated cardiomyopathy and the type, patterns, and course of fibrosis reveals fibrosis progression in genetic patients.

Journal: Kardiologia polska

Published: July 31, 2025

The Quiet Burden of Iron: A Rare Case of Hereditary Hemochromatosis in Pakistan.

Journal: Cureus

Published: July 19, 2025

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Leveraging a Genetic Proxy to Investigate the Effects of Lifelong Cardiac Sodium Channel Blockade.

Leveraging a Genetic Proxy to Investigate the Effects of Lifelong Cardiac Sodium Channel Blockade.

Decoding MTSS1: Turning Genetic Clues into Cardiac Cures.

Decoding MTSS1: Turning Genetic Clues into Cardiac Cures.

Charting the genetic landscape of dilated cardiomyopathy in Poland: first insights from a national perspective.

Charting the genetic landscape of dilated cardiomyopathy in Poland: first insights from a national perspective.

Survival, clinical, and genetic findings in paediatric cardiomyopathy: a five-year prospective study from Brazil.

Survival, clinical, and genetic findings in paediatric cardiomyopathy: a five-year prospective study from Brazil.

Sex Differences in Prognosis of Patients With Genetic Dilated Cardiomyopathy.

Sex Differences in Prognosis of Patients With Genetic Dilated Cardiomyopathy.

Genetic factors for risk stratification in dilated cardiomyopathy

Genetic factors for risk stratification in dilated cardiomyopathy

Genetic architecture of dilated cardiomyopathy in Poland: variant distribution, clinical characteristics, and prognosis.

Genetic architecture of dilated cardiomyopathy in Poland: variant distribution, clinical characteristics, and prognosis.

Predictive value of ambulatory ECG monitoring for malignant arrhythmic events in genetic dilated cardiomyopathy.

Predictive value of ambulatory ECG monitoring for malignant arrhythmic events in genetic dilated cardiomyopathy.

CRYAB Missense Mutation Reveals Shared Pathogenesis of Familial Cardiomyopathy and Arrhythmia.

CRYAB Missense Mutation Reveals Shared Pathogenesis of Familial Cardiomyopathy and Arrhythmia.

Early Detection of Subclinical Myocardial Dysfunction in Familial Dilated Cardiomyopathy Using Myocardial Work Analysis.

Early Detection of Subclinical Myocardial Dysfunction in Familial Dilated Cardiomyopathy Using Myocardial Work Analysis.

Investigation into the relationship between the etiology of dilated cardiomyopathy and the type, patterns, and course of fibrosis reveals fibrosis progression in genetic patients.

Investigation into the relationship between the etiology of dilated cardiomyopathy and the type, patterns, and course of fibrosis reveals fibrosis progression in genetic patients.

The Quiet Burden of Iron: A Rare Case of Hereditary Hemochromatosis in Pakistan.

The Quiet Burden of Iron: A Rare Case of Hereditary Hemochromatosis in Pakistan.