Search Results (57)
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Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected].Academic Article Why?
Clinical approach to genetic testing in amyloid cardiomyopathy: from mechanism to effective therapies.Academic Article Why?
Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review.Academic Article Why?
Amyloid Cardiomyopathy: Disease on the Rise.Academic Article Why?
Light Chain Testing Abnormalities Among Patients With Transthyretin Amyloid Cardiomyopathy Referred for Technetium-99m Pyrophosphate Imaging.Academic Article Why?
Molecular Imaging of Primary Amyloid CardiomyopathyGrant Why?
Molecular Imaging of Primary Amyloid CardiomyopathyGrant Why?
Diflunisal treatment is associated with improved survival for patients with early stage wild-type transthyretin (ATTR) amyloid cardiomyopathy: the Boston University Amyloidosis Center experience.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?
Efficacy of Tafamidis in Patients With Hereditary and Wild-Type Transthyretin Amyloid Cardiomyopathy: Further Analyses From ATTR-ACT.Academic Article Why?
"A Phase 3, Randomized, Double-Blind, Placebo-controlled Study of the Efficacy and Safety of AG10 in Subjects with Symptomatic Transthyretin Amyloid Cardiomyopathy"Grant Why?
A Randomised, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of GSK2998728 in Subjects with Transthyretin Amyloid Cardiomyopathy, FAC204650Grant Why?
An Open-Label Extension and Safety Monitoring Study of Acoramidis (AG10) in Participants with Symptomatic Transthyretin Amyloid Cardiomyopathy Who Completed the Phase 3 ATTRibute-CM Trial (AG10-301)Grant Why?
Familial wild-type transthyretin cardiomyopathy.Academic Article Why?
Cardiac amyloidosis: An update on pathophysiology, diagnosis, and treatment.Academic Article Why?
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  • Amyloid
  • Cardiomyopathy
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