Search Results (30)
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Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected].Academic Article Why?
Amyloid Cardiomyopathy: Disease on the Rise.Academic Article Why?
Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review.Academic Article Why?
Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS).Academic Article Why?
Familial wild-type transthyretin cardiomyopathy.Academic Article Why?
Cardiac amyloidosis: An update on pathophysiology, diagnosis, and treatment.Academic Article Why?
Amyloidotic cardiomyopathy: multidisciplinary approach to diagnosis and treatment.Academic Article Why?
Matrix metalloproteinases and their tissue inhibitors in cardiac amyloidosis: relationship to structural, functional myocardial changes and to light chain amyloid deposition.Academic Article Why?
The diagnosis and typing of cardiac amyloidosis.Academic Article Why?
Can 99mTc-Pyrophosphate Aid in Early Detection of Cardiac Involvement in Asymptomatic Variant TTR Amyloidosis?Academic Article Why?
Circulating matrix metalloproteinases and tissue inhibitors of metalloproteinases in cardiac amyloidosis.Academic Article Why?
Direct tissue evaluation via immunofluorescence: in the diagnosis of hereditary transthyretin cardiac amyloidosis.Academic Article Why?
Homozygosity for the V122I mutation in transthyretin is associated with earlier onset of cardiac amyloidosis in the African American population in the seventh decade of life.Academic Article Why?
Identification of Transthyretin Cardiac Amyloidosis Using Serum Retinol-Binding Protein 4 and a Clinical Prediction Model.Academic Article Why?
Nuclear tracers for transthyretin cardiac amyloidosis: time to bone up?Academic Article Why?
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