: Cardiac amyloidosis is an infiltrative disorder caused by transthyretin or immunoglobulin free light-chain deposition, which determines clinical disease with similar phenotype but different time course, prognosis and therapy. Multimodality imaging is the cornerstone for disease diagnosis and management. Multimodality imaging has revolutionized the approach to the disease favoring its awareness and simplifying its diagnosis, especially in ATTR cardiac amyloidosis. This describes the different imaging tools, from the traditional to the more novel ones, and highlights the different approach in each different setting (prognosis, subtyping, prognosis, monitoring disease progression, and response to therapy)
Cardiac amyloidosis is a restrictive infiltrative cardiomyopathy burdened by high mortality. The two...
Amyloidosis results from insoluble precursor proteins being deposited in the extracellular compartme...
none5siAdvances in cardiac imaging have resulted in greater recognition of cardiac amyloidosis in ev...
: Cardiac amyloidosis is an infiltrative disorder caused by transthyretin or immunoglobulin free lig...
Amyloidosis is a systemic infiltrative disease, in which unstable proteins misfold, form aggregates ...
Systemic amyloidosis encompasses a debilitating, under-diagnosed but increasingly recognized group o...
Abstract Background Cardiac Amyloidosis (CA) pertains to the cardiac involvement of a group of disea...
Amyloidosis is a progressive infiltrative disease instigated by the extracellular deposition of amyl...
Cardiac amyloidosis (CA) is a disease characterized by the deposition of misfolded protein deposits ...
International audienceAmyloidosis is a severe systemic disease. Cardiac involvement may occur in the...
BACKGROUND Cardiac amyloidosis is a progressive infiltrative disease for which new treatments are...
SummaryAmyloidosis is a severe systemic disease. Cardiac involvement may occur in the three main typ...
ContextAmyloidosis(A) prognosis is determined by cardiac involvement.The main types of A are immunog...
Cardiac amyloidosis is a rare, infiltrative cardiomyopathy that presents with thickened ventricular ...
Cardiac involvement in systemic amyloidosis, due either to immunoglobulin light-chain or transthyret...
Cardiac amyloidosis is a restrictive infiltrative cardiomyopathy burdened by high mortality. The two...
Amyloidosis results from insoluble precursor proteins being deposited in the extracellular compartme...
none5siAdvances in cardiac imaging have resulted in greater recognition of cardiac amyloidosis in ev...
: Cardiac amyloidosis is an infiltrative disorder caused by transthyretin or immunoglobulin free lig...
Amyloidosis is a systemic infiltrative disease, in which unstable proteins misfold, form aggregates ...
Systemic amyloidosis encompasses a debilitating, under-diagnosed but increasingly recognized group o...
Abstract Background Cardiac Amyloidosis (CA) pertains to the cardiac involvement of a group of disea...
Amyloidosis is a progressive infiltrative disease instigated by the extracellular deposition of amyl...
Cardiac amyloidosis (CA) is a disease characterized by the deposition of misfolded protein deposits ...
International audienceAmyloidosis is a severe systemic disease. Cardiac involvement may occur in the...
BACKGROUND Cardiac amyloidosis is a progressive infiltrative disease for which new treatments are...
SummaryAmyloidosis is a severe systemic disease. Cardiac involvement may occur in the three main typ...
ContextAmyloidosis(A) prognosis is determined by cardiac involvement.The main types of A are immunog...
Cardiac amyloidosis is a rare, infiltrative cardiomyopathy that presents with thickened ventricular ...
Cardiac involvement in systemic amyloidosis, due either to immunoglobulin light-chain or transthyret...
Cardiac amyloidosis is a restrictive infiltrative cardiomyopathy burdened by high mortality. The two...
Amyloidosis results from insoluble precursor proteins being deposited in the extracellular compartme...
none5siAdvances in cardiac imaging have resulted in greater recognition of cardiac amyloidosis in ev...