BACKGROUND: Cardiac amyloidosis is an underdiagnosed condition and simple methods for accurate diagnosis are warranted. We aimed to validate a novel, dual-modality approach to identify transthyretin cardiac amyloidosis (ATTR-CA), employing echocardiographic relative wall thickness (RWT), and ECG S-wave from aVR (SaVR), and compare its accuracy with conventional echocardiographic approaches. MATERIAL AND METHODS: We investigated 102 patients with ATTR-CA and 65 patients with left ventricular hypertrophy (LVH), all with septal thickness > 14 mm. We validated the accuracy of echocardiographic measures, including RWT, RWT/SaVR, posterior wall thickness (PWT), LV mass index (LVMI), left atrial volume index (LAVI), global longitudinal stra...
Objectives This study aimed to investigate the accuracy of a broad range of echocardiographic variab...
Background-Cardiac transthyretin (ATTR) amyloidosis is a progressive and fatal cardiomyopathy for wh...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...
BACKGROUND: Cardiac amyloidosis is an underdiagnosed condition and simple methods for accurate diagn...
AIMS/BACKGROUND: Transthyretin amyloid (ATTR) amyloidosis cardiomyopathy is an underdiagnosed, causa...
BACKGROUND: Reduced LV longitudinal strain (GLS) and increased relative apical sparing (RELAPS) and ...
Aims: Cardiac amyloidosis (CA) affects the four heart chambers, which can all be evaluated through s...
The aims of the study were to explore the ability of native myocardial T1 mapping by cardiac magneti...
Background: Cardiac amyloidosis (CA) is cardiomyopathy with a hypertrophic phenotype characterised b...
Aims: Cardiac amyloidosis (CA) is due to a deposition of amyloid fibrils in the heart causing an inc...
From First European Congress on Hereditary ATTR amyloidosisParis, France. 2-3 November 2015Internati...
ObjectivesWe sought to evaluate noninvasive parameters by electrocardiography, echocardiography, tec...
OBJECTIVES: The aims of the study were to explore the ability of native myocardial T1 mapping by car...
Background: Cardiac transthyretin (ATTR) amyloidosis is a progressive and fatal cardiomyopathy for w...
Objectives This study aimed to investigate the accuracy of a broad range of echocardiographic variab...
Background-Cardiac transthyretin (ATTR) amyloidosis is a progressive and fatal cardiomyopathy for wh...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...
BACKGROUND: Cardiac amyloidosis is an underdiagnosed condition and simple methods for accurate diagn...
AIMS/BACKGROUND: Transthyretin amyloid (ATTR) amyloidosis cardiomyopathy is an underdiagnosed, causa...
BACKGROUND: Reduced LV longitudinal strain (GLS) and increased relative apical sparing (RELAPS) and ...
Aims: Cardiac amyloidosis (CA) affects the four heart chambers, which can all be evaluated through s...
The aims of the study were to explore the ability of native myocardial T1 mapping by cardiac magneti...
Background: Cardiac amyloidosis (CA) is cardiomyopathy with a hypertrophic phenotype characterised b...
Aims: Cardiac amyloidosis (CA) is due to a deposition of amyloid fibrils in the heart causing an inc...
From First European Congress on Hereditary ATTR amyloidosisParis, France. 2-3 November 2015Internati...
ObjectivesWe sought to evaluate noninvasive parameters by electrocardiography, echocardiography, tec...
OBJECTIVES: The aims of the study were to explore the ability of native myocardial T1 mapping by car...
Background: Cardiac transthyretin (ATTR) amyloidosis is a progressive and fatal cardiomyopathy for w...
Objectives This study aimed to investigate the accuracy of a broad range of echocardiographic variab...
Background-Cardiac transthyretin (ATTR) amyloidosis is a progressive and fatal cardiomyopathy for wh...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...