Abstract 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. Objectives: To characterize the volumetric and functional properties of the right atrium (RA) in AL-CA by three-dimensional speckle-tracking echocardiography (3DSTE). Methods: A total of 16 patients (mean age: 64.5 ± 10.1 years, 11 males) with AL-CA were examined. Their results were compared to that of 15 age- and gender-matched healthy controls (mean age: 58.9 ± 6.9 years, 8 males). All cases have undergone complete two-dimensional Doppler and 3DSTE. A two-tailed p ...
Objectives: The aim was to determine the role of assessing right ventricular (RV) function, using st...
Objectives This study aimed to investigate the accuracy of a broad range of echocardiographic variab...
Cardiac amyloidosis (CA) is of poor prognosis and has three main causes: light chain (AL), hereditar...
Abstract Background: Light-chain (AL) cardiac amyloidosis (CA) is characterized by fibril deposits,...
Background: Light-chain (AL) cardiac amyloidosis (CA) is characterized by fibril deposits, which are...
INTRODUCTION: While cardiac amyloidosis (CA) is a rare systemic disease characterized by extracellul...
Background. Given that in patients with cardiac amyloidosis(CA), deposition of amyloid protein is no...
International audienceBACKGROUND:Systemic light chain amyloidosis (AL) is characterized by the extra...
BACKGROUND: Cardiac amyloidosis (CA) is a rare condition characterized by the extracellular depositi...
\(\bf Background:\) Cardiac amyloidosis (CA) manifests in a hypertrophic phenotype with a poor progn...
Aims: Cardiac amyloidosis (CA) affects the four heart chambers, which can all be evaluated through s...
Echocardiographic diagnosis of cardiac amyloidosis (CA) can be difficult to differentiate from incre...
The dataset presented in this article is related to the research article entitled “Biventricular ass...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...
Objectives: The aim was to determine the role of assessing right ventricular (RV) function, using st...
Objectives This study aimed to investigate the accuracy of a broad range of echocardiographic variab...
Cardiac amyloidosis (CA) is of poor prognosis and has three main causes: light chain (AL), hereditar...
Abstract Background: Light-chain (AL) cardiac amyloidosis (CA) is characterized by fibril deposits,...
Background: Light-chain (AL) cardiac amyloidosis (CA) is characterized by fibril deposits, which are...
INTRODUCTION: While cardiac amyloidosis (CA) is a rare systemic disease characterized by extracellul...
Background. Given that in patients with cardiac amyloidosis(CA), deposition of amyloid protein is no...
International audienceBACKGROUND:Systemic light chain amyloidosis (AL) is characterized by the extra...
BACKGROUND: Cardiac amyloidosis (CA) is a rare condition characterized by the extracellular depositi...
\(\bf Background:\) Cardiac amyloidosis (CA) manifests in a hypertrophic phenotype with a poor progn...
Aims: Cardiac amyloidosis (CA) affects the four heart chambers, which can all be evaluated through s...
Echocardiographic diagnosis of cardiac amyloidosis (CA) can be difficult to differentiate from incre...
The dataset presented in this article is related to the research article entitled “Biventricular ass...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...
Objectives: The aim was to determine the role of assessing right ventricular (RV) function, using st...
Objectives This study aimed to investigate the accuracy of a broad range of echocardiographic variab...
Cardiac amyloidosis (CA) is of poor prognosis and has three main causes: light chain (AL), hereditar...