BACKGROUND: Light chain (AL) and transthyretin (ATTR) amyloid fibrils are deposited in the extracellular space of the myocardium, resulting in heart failure and premature mortality. Extracellular expansion can be quantified by computed tomography, offering a rapid, cheaper, and more practical alternative to cardiac magnetic resonance, especially among patients with cardiac devices or on renal dialysis. OBJECTIVES: This study sought to investigate the association of extracellular volume fraction by computed tomography (ECVCT), myocardial remodeling, and mortality in patients with systemic amyloidosis. METHODS: Patients with confirmed systemic amyloidosis and varying degrees of cardiac involvement underwent electrocardiography-gated cardiac c...
Introduction: Systemic amyloidosis is characterised by the extracellular deposition of amyloid fibri...
BACKGROUND: Management of cardiac amyloidosis (CA) is related to amyloid deposition. Our aim was to ...
Objectives: In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aim...
BACKGROUND: Prognosis in light-chain (AL) and transthyretin (ATTR) amyloidosis is influenced by card...
Cardiac involvement determines outcome in patients with systemic amyloidosis. There is major unmet n...
PURPOSE: To investigate cardiac magnetic resonance (MR) imaging measurements of extracellular volume...
Background: T1 mapping allows quantitative assessment of “diffuse” deposition of amyloid protein in ...
AIMS: To assess the prognostic value of myocardial pre-contrast T1 and extracellular volume (ECV) in...
Early diagnosis is crucial for the improvement of outcomes of patients with cardiac amyloidosis (CA)...
A 67-year-old Caucasian man presented with atrial flutter on routine 12-lead electrocardiography (EC...
Abstract Cardiovascular magnetic resonance (CMR) plays an important clinical role for diagnosis and ...
ObjectivesThis study tested the diagnostic and prognostic utility of a rapid, visual T1 assessment m...
OBJECTIVES: In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aim...
Amyloidosis is a systemic infiltrative disorder in whichinsoluble protein fibrils are deposited in t...
BACKGROUND: The prognosis and treatment of the 2 main types of cardiac amyloidosis, immunoglobulin l...
Introduction: Systemic amyloidosis is characterised by the extracellular deposition of amyloid fibri...
BACKGROUND: Management of cardiac amyloidosis (CA) is related to amyloid deposition. Our aim was to ...
Objectives: In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aim...
BACKGROUND: Prognosis in light-chain (AL) and transthyretin (ATTR) amyloidosis is influenced by card...
Cardiac involvement determines outcome in patients with systemic amyloidosis. There is major unmet n...
PURPOSE: To investigate cardiac magnetic resonance (MR) imaging measurements of extracellular volume...
Background: T1 mapping allows quantitative assessment of “diffuse” deposition of amyloid protein in ...
AIMS: To assess the prognostic value of myocardial pre-contrast T1 and extracellular volume (ECV) in...
Early diagnosis is crucial for the improvement of outcomes of patients with cardiac amyloidosis (CA)...
A 67-year-old Caucasian man presented with atrial flutter on routine 12-lead electrocardiography (EC...
Abstract Cardiovascular magnetic resonance (CMR) plays an important clinical role for diagnosis and ...
ObjectivesThis study tested the diagnostic and prognostic utility of a rapid, visual T1 assessment m...
OBJECTIVES: In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aim...
Amyloidosis is a systemic infiltrative disorder in whichinsoluble protein fibrils are deposited in t...
BACKGROUND: The prognosis and treatment of the 2 main types of cardiac amyloidosis, immunoglobulin l...
Introduction: Systemic amyloidosis is characterised by the extracellular deposition of amyloid fibri...
BACKGROUND: Management of cardiac amyloidosis (CA) is related to amyloid deposition. Our aim was to ...
Objectives: In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aim...