Genotype, echocardiography, and survival in familial transthyretin amyloidosis

Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: The Transthyretin Amyloidosis Cardiac Study (TRACS)

(2012) Frederick L. Ruberg et al.   AMERICAN HEART JOURNAL

THAOS – The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis

(2012) Teresa Coelho et al.   CURRENT MEDICAL RESEARCH AND OPINION

Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective

(2012) C. Rapezzi et al.   EUROPEAN HEART JOURNAL

Development of cardiomyopathy after liver transplantation in Swedish hereditary transthyretin amyloidosis (ATTR) patients

(2011) Sadahisa Okamoto et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant

(2011) P. T. Sattianayagam et al.   EUROPEAN HEART JOURNAL

Significance of the amyloidogenic transthyretin Val 122 Ile allele in African Americans in the Arteriosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) Studies

(2010) Joel Buxbaum et al.   AMERICAN HEART JOURNAL

Transthyretin-related amyloidoses and the heart: a clinical overview

(2010) Claudio Rapezzi et al.   Nature Reviews Cardiology

Cardiac amyloidosis in African Americans: Comparison of clinical and laboratory features of transthyretin V122I amyloidosis and immunoglobulin light chain amyloidosis

(2009) Lawreen H. Connors et al.   AMERICAN HEART JOURNAL

Systemic Cardiac Amyloidoses

(2009) Claudio Rapezzi et al.   CIRCULATION

Unlocking the Mysteries of Diastolic Function

(2008) Steven J. Lester et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY