Phenotypic profile of Ile68Leu transthyretin amyloidosis: an underdiagnosed cause of heart failure

A new staging system for cardiac transthyretin amyloidosis

(2017) Julian D Gillmore et al.   EUROPEAN HEART JOURNAL

Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths

(2017) Esther González-López et al.   EUROPEAN HEART JOURNAL

Transthyretin V122I (pV142I)* cardiac amyloidosis: an age-dependent autosomal dominant cardiomyopathy too common to be overlooked as a cause of significant heart disease in elderly African Americans

(2017) Joel N. Buxbaum et al.   GENETICS IN MEDICINE

Amyloid heart disease: genetics translated into disease-modifying therapy

(2017) Brett W Sperry et al.   HEART

Reply

(2017) Mathew S. Maurer et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Val122Ile mt-ATTR Has a Worse Survival Than wt-ATTR Cardiac Amyloidosis

(2017) Avinainder Singh et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Genotype and Phenotype of Transthyretin Cardiac Amyloidosis

(2016) Mathew S. Maurer et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Natural History of Wild-Type Transthyretin Cardiac Amyloidosis and Risk Stratification Using a Novel Staging System

(2016) Martha Grogan et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Cardiac amyloidosis: the great pretender

(2015) Claudio Rapezzi et al.   HEART FAILURE REVIEWS

The Amyloidogenic V122I Transthyretin Variant in Elderly Black Americans

(2015) C. Cristina Quarta et al.   NEW ENGLAND JOURNAL OF MEDICINE

Amyloid Cardiomyopathy in Hereditary Transthyretin V30M Amyloidosis - Impact of Sex and Amyloid Fibril Composition

(2015) Sandra Arvidsson et al.   PLoS One

The myocardial contraction fraction is superior to ejection fraction in predicting survival in patients with AL cardiac amyloidosis

(2014) Amanda Tendler et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

Online Registry for Mutations in Hereditary Amyloidosis Including Nomenclature Recommendations

(2014) Dorota M. Rowczenio et al.   HUMAN MUTATION

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

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

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

Heart complications in familial transthyretin amyloidosis: impact of age and gender

(2010) Rolf Hörnsten et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS