<p><i>Data are presented as median (interquartile range)</i>, <i>unless stated otherwise</i>. <i>Type A</i>, <i>amyloid fibril composed of a mixture of full length and fragmented transthyretin; Type B</i>, <i>full length transthyretin only; IVST</i>, <i>interventricular septal thickness; PWT</i>, <i>posterior wall thickness; LVDD</i>, <i>left ventricular diastolic diameter; LVSD</i>, <i>left ventricular systolic diameter; LVMI</i>, <i>Left ventricular mass index; LAVI</i>, <i>left atrial volume index; LVEF</i>, <i>left ventricular ejection fraction; E/A; early/late mitral diastolic filling velocity; E/em</i>, <i>early mitral diastolic filling/early myocardial diastolic filling velocity; IVRT</i>, <i>Isovolumic relaxation time; SV</i>, <i>st...
Background: Hereditary transthyretin amyloidosis (ATTR) is a lethal disease in which misfolded trans...
AIMS/BACKGROUND: Transthyretin amyloid (ATTR) amyloidosis cardiomyopathy is an underdiagnosed, causa...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...
BACKGROUND: Few studies have analyzed the clinical and echocardiographic differences between light-c...
Aims: Cardiac amyloidosis (CA) is due to a deposition of amyloid fibrils in the heart causing an inc...
PURPOSE: Transthyretin V30M (ATTR V30M) amyloidosis is a phenotypically diverse disease with symptom...
Background: Cardiac amyloidosis (CA) is cardiomyopathy with a hypertrophic phenotype characterised b...
BACKGROUND: Signs of cardiac transthyretin (TTR) amyloidosis (ATTR) in patients with echocardiograph...
Background Hereditary transthyretin amyloid (ATTRm) amyloidosis is a systemic disease mainly affecti...
BACKGROUND: Management of cardiac amyloidosis (CA) is related to amyloid deposition. Our aim was to ...
Background - : Immunoglobulin amyloid light-chain (AL)-related cardiac amyloidosis (CA) has a worse ...
BACKGROUND: Management of cardiac amyloidosis (CA) is related to amyloid deposition. Our aim was to ...
Background: Mutated transthyretin-associated (ATTRm) amyloidosis with heart failure is associated wi...
Aim: Mutated transthyretin (TTRv) cardiac amyloidosis (CA) represents an uncommon form of CA. Our st...
Background: Hereditary transthyretin amyloidosis (ATTR) is a lethal disease in which misfolded trans...
AIMS/BACKGROUND: Transthyretin amyloid (ATTR) amyloidosis cardiomyopathy is an underdiagnosed, causa...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...
BACKGROUND: Few studies have analyzed the clinical and echocardiographic differences between light-c...
Aims: Cardiac amyloidosis (CA) is due to a deposition of amyloid fibrils in the heart causing an inc...
PURPOSE: Transthyretin V30M (ATTR V30M) amyloidosis is a phenotypically diverse disease with symptom...
Background: Cardiac amyloidosis (CA) is cardiomyopathy with a hypertrophic phenotype characterised b...
BACKGROUND: Signs of cardiac transthyretin (TTR) amyloidosis (ATTR) in patients with echocardiograph...
Background Hereditary transthyretin amyloid (ATTRm) amyloidosis is a systemic disease mainly affecti...
BACKGROUND: Management of cardiac amyloidosis (CA) is related to amyloid deposition. Our aim was to ...
Background - : Immunoglobulin amyloid light-chain (AL)-related cardiac amyloidosis (CA) has a worse ...
BACKGROUND: Management of cardiac amyloidosis (CA) is related to amyloid deposition. Our aim was to ...
Background: Mutated transthyretin-associated (ATTRm) amyloidosis with heart failure is associated wi...
Aim: Mutated transthyretin (TTRv) cardiac amyloidosis (CA) represents an uncommon form of CA. Our st...
Background: Hereditary transthyretin amyloidosis (ATTR) is a lethal disease in which misfolded trans...
AIMS/BACKGROUND: Transthyretin amyloid (ATTR) amyloidosis cardiomyopathy is an underdiagnosed, causa...
Background: The extent of right ventricular (RV) involvement in transthyretin amyloidosis (ATTR) is ...