Objective: To assess the usefulness of bone scintigraphy with (99m)Technetium-hydroxymethylene diphosphonate (Tc-99m-HDP) for the detection of cardiac involvement in a group of patients with ATTR amyloidosis in different phases of disease, to relate the findings to echocardiography, ECG and cardiac biomarkers, and to evaluate different bone scintigraphic techniques and calculation methods for quantification of the cardiac uptake and for correlation with echocardiographic features and cardiac biomarkers.Methods: Forty-one patients underwent clinical examinations, echocardiography, ECG, measurement of cardiac biomarkers and bone scintigraphy (planar imaging and SPECT-CT) and were subsequently subdivided into three groups: (1) carriers of an a...
Aims: There has been a paradigm shift in diagnosis of cardiac transthyretin amyloidosis (ATTR) with ...
Purpose: Cardiac transthyretin amyloidosis is a usually fatal form of restrictive cardiomyopathy for...
Objectives: In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aim...
Objective: To assess the usefulness of bone scintigraphy with (99m)Technetium-hydroxymethylene dipho...
Cardiac amyloidosis (CA) is a life-threatening disease caused by extracellular deposition of amyloid...
Background: 99mTc-labelled bisphosphonates are used for imaging assessment of patients with transthy...
We investigated the diagnostic accuracy of (99m)Tc-3,3- diphosphono-1,2-propanodicarboxylic acid ((9...
Transthyretin-related cardiac amyloidosis (ATTR) amyloidosis is an aggressive, rapidly progressive, ...
PURPOSE: Cardiac transthyretin-related amyloidosis (ATTR) is a progressive and fatal cardiomyopathy....
Transthyretin cardiac amyloidosis (ATTR) is a rare cardiac protein deposition disease characterized ...
EPS-066 Aim/Introduction: To analyze the influence of the determination of free monoclonal proteins ...
Cardiac amyloidosis (CA) is characterized by extracellular deposition of protein-derived fibrils and...
ObjectivesWe investigated the diagnostic accuracy of 99mTc-3,3-diphosphono-1,2-propanodicarboxylic a...
Cardiac transthyretin-related amyloidosis (ATTR) is a progressive and fatal cardiomyopathy. The diag...
Purpose: Transthyretin (ATTR) amyloidosis is a rare but serious infiltrative disease associated with...
Aims: There has been a paradigm shift in diagnosis of cardiac transthyretin amyloidosis (ATTR) with ...
Purpose: Cardiac transthyretin amyloidosis is a usually fatal form of restrictive cardiomyopathy for...
Objectives: In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aim...
Objective: To assess the usefulness of bone scintigraphy with (99m)Technetium-hydroxymethylene dipho...
Cardiac amyloidosis (CA) is a life-threatening disease caused by extracellular deposition of amyloid...
Background: 99mTc-labelled bisphosphonates are used for imaging assessment of patients with transthy...
We investigated the diagnostic accuracy of (99m)Tc-3,3- diphosphono-1,2-propanodicarboxylic acid ((9...
Transthyretin-related cardiac amyloidosis (ATTR) amyloidosis is an aggressive, rapidly progressive, ...
PURPOSE: Cardiac transthyretin-related amyloidosis (ATTR) is a progressive and fatal cardiomyopathy....
Transthyretin cardiac amyloidosis (ATTR) is a rare cardiac protein deposition disease characterized ...
EPS-066 Aim/Introduction: To analyze the influence of the determination of free monoclonal proteins ...
Cardiac amyloidosis (CA) is characterized by extracellular deposition of protein-derived fibrils and...
ObjectivesWe investigated the diagnostic accuracy of 99mTc-3,3-diphosphono-1,2-propanodicarboxylic a...
Cardiac transthyretin-related amyloidosis (ATTR) is a progressive and fatal cardiomyopathy. The diag...
Purpose: Transthyretin (ATTR) amyloidosis is a rare but serious infiltrative disease associated with...
Aims: There has been a paradigm shift in diagnosis of cardiac transthyretin amyloidosis (ATTR) with ...
Purpose: Cardiac transthyretin amyloidosis is a usually fatal form of restrictive cardiomyopathy for...
Objectives: In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aim...