Background: Light-chain (AL) cardiac amyloidosis (CA) is characterized by fibril deposits, which are composed of monoclonal immunoglobulin light chains. The right ventricle is mostly involved in AL-CA and impairment of its function is a predictor of worse prognosis
AIM: The importance of right ventricle (RV) dysfunction in AL amyloidosis has been underestimated. T...
Introduction: Systemic amyloidosis is characterised by the extracellular deposition of amyloid fibri...
Objectives: The aim of this study was to characterize left atrial (LA) pathology in explanted hearts...
Abstract Background: Light-chain (AL) cardiac amyloidosis (CA) is characterized by fibril deposits,...
The dataset presented in this article is related to the research article entitled “Biventricular ass...
INTRODUCTION: While cardiac amyloidosis (CA) is a rare systemic disease characterized by extracellul...
International audienceBACKGROUND:Systemic light chain amyloidosis (AL) is characterized by the extra...
Background. Given that in patients with cardiac amyloidosis(CA), deposition of amyloid protein is no...
Objectives: The aim was to determine the role of assessing right ventricular (RV) function, using st...
BACKGROUND: Cardiac amyloidosis (CA) is a rare condition characterized by the extracellular depositi...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...
Aims: Cardiac amyloidosis (CA) affects the four heart chambers, which can all be evaluated through s...
Cardiac amyloidosis (CA) is of poor prognosis and has three main causes: light chain (AL), hereditar...
\(\bf Background:\) Cardiac amyloidosis (CA) manifests in a hypertrophic phenotype with a poor progn...
Background: In recent studies, alterations in ventricular deformations were demonstrated in adult pa...
AIM: The importance of right ventricle (RV) dysfunction in AL amyloidosis has been underestimated. T...
Introduction: Systemic amyloidosis is characterised by the extracellular deposition of amyloid fibri...
Objectives: The aim of this study was to characterize left atrial (LA) pathology in explanted hearts...
Abstract Background: Light-chain (AL) cardiac amyloidosis (CA) is characterized by fibril deposits,...
The dataset presented in this article is related to the research article entitled “Biventricular ass...
INTRODUCTION: While cardiac amyloidosis (CA) is a rare systemic disease characterized by extracellul...
International audienceBACKGROUND:Systemic light chain amyloidosis (AL) is characterized by the extra...
Background. Given that in patients with cardiac amyloidosis(CA), deposition of amyloid protein is no...
Objectives: The aim was to determine the role of assessing right ventricular (RV) function, using st...
BACKGROUND: Cardiac amyloidosis (CA) is a rare condition characterized by the extracellular depositi...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...
Aims: Cardiac amyloidosis (CA) affects the four heart chambers, which can all be evaluated through s...
Cardiac amyloidosis (CA) is of poor prognosis and has three main causes: light chain (AL), hereditar...
\(\bf Background:\) Cardiac amyloidosis (CA) manifests in a hypertrophic phenotype with a poor progn...
Background: In recent studies, alterations in ventricular deformations were demonstrated in adult pa...
AIM: The importance of right ventricle (RV) dysfunction in AL amyloidosis has been underestimated. T...
Introduction: Systemic amyloidosis is characterised by the extracellular deposition of amyloid fibri...
Objectives: The aim of this study was to characterize left atrial (LA) pathology in explanted hearts...