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Elektrokardiographische Korrelate der Krankheitslast bei kardialer Transthyretin-Amyloidose

Trajectory and Prognostic Significance of Conduction System Disease in Cardiac Transthyretin Amyloidosis: A Multicenter Study

Prognostic predictors in patients with cardiac ATTR Amyloidosis and changes with ATTR-specific therapy: data from the Amyloidosis Center Lower Saxony

Treatment Patterns and Clinical Decision-Making in Cardiac Transthyretin Amyloidosis: a Multicentre Study

Prevalence of iron deficiency and influence of treatment with TTR stabilizers on patients with wild type ATTR amyloidosis without anaemia

Transthyretin Stabilizer Therapy increases naturally-occurring Antibodies in ATTR Cardiomyopathy

The Effect of Different Exercise Modalities on the Maximal Left Ventricular Outflow Tract Gradient in Patients with Obstructive Hypertrophic Cardiomyopathy

Mavacamten Treatment in Obstructive Hypertrophic Cardiomyopathy: Results from the Multi-centric TranslatiOnal Registry for CardiomyopatHies-Plus (TORCH-Plus-DZHK21)

Comparison of Transcoronary Ablation of Septal Hypertrophy (TASH) and Mavacamten treatment in Patients with Obstructive Hypertrophic Cardiomyopathy: A Single-Center Study

Personalized mapping of myocardial bioenergetics reveals genotype-linked metabolic signatures in hypertrophic cardiomyopathy

Prevalence and Clinical Impact of Cardiomyopathy-associated Rare Variants in Large Scale Cohorts

Mavacamten versus alcohol septal ablation: clinical, echocardiographic, and patient-reported outcomes after 3 months

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