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Match | Type | Why |
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Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected]. | Academic Article |
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Clinical approach to genetic testing in amyloid cardiomyopathy: from mechanism to effective therapies. | Academic Article |
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Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review. | Academic Article |
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Amyloid Cardiomyopathy: Disease on the Rise. | Academic Article |
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Light Chain Testing Abnormalities Among Patients With Transthyretin Amyloid Cardiomyopathy Referred for Technetium-99m Pyrophosphate Imaging. | Academic Article |
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Molecular Imaging of Primary Amyloid Cardiomyopathy | Grant |
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Molecular Imaging of Primary Amyloid Cardiomyopathy | Grant |
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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 |
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Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS). | Academic Article |
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Efficacy of Tafamidis in Patients With Hereditary and Wild-Type Transthyretin Amyloid Cardiomyopathy: Further Analyses From ATTR-ACT. | Academic Article |
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"A Phase 3, Randomized, Double-Blind, Placebo-controlled Study of the Efficacy and Safety of AG10 in Subjects with Symptomatic Transthyretin Amyloid Cardiomyopathy" | Grant |
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A Randomised, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of GSK2998728 in Subjects with Transthyretin Amyloid Cardiomyopathy, FAC204650 | Grant |
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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 |
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Familial wild-type transthyretin cardiomyopathy. | Academic Article |
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Cardiac amyloidosis: An update on pathophysiology, diagnosis, and treatment. | Academic Article |
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