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Publications by Claudio Tinoco Mesquita
Cardiomyopathy Related to Transthyretin Val30met Mutation in Hereditary Systemic Amyloidosis
ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR
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Widespread Cardiac and Vasomotor Autonomic Dysfunction in Non-Val30Met Hereditary Transthyretin Amyloidosis
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The V122I Mutation in Hereditary Transthyretin-Mediated Amyloidosis Is Significantly Associated With Polyneuropathy
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Hereditary ATTR Amyloidosis With Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)
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Identifying Mixed Phenotype: Evaluating the Presence of Polyneuropathy in Patients With Hereditary Transthyretin-Mediated Amyloidosis With Cardiomyopathy
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Fibroblasts Endocytose and Degrade Transthyretin Aggregates in Transthyretin-Related Amyloidosis
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Cardiac Findings and Events Observed in an Open-Label Clinical Trial of Tafamidis in Patients With Non-Val30Met and Non-Val122Ile Hereditary Transthyretin Amyloidosis
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Tafamidis for Autonomic Neuropathy in Hereditary Transthyretin (ATTR) Amyloidosis: A Review
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An Unusual Case of Hereditary Transthyretin‐related Amyloidosis and Ulcerative Colitis in a Young Indian Girl
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Mutation in Gelsolin Gene in Finnish Hereditary Amyloidosis
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