Asp58Ala is the Predominant Mutation of theTTRGene in Korean Patients with Hereditary Transthyretin-Related Amyloidosis

Left Ventricular Structure and Function in Transthyretin-Related Versus Light-Chain Cardiac Amyloidosis

(2014) Candida Cristina Quarta et al.   CIRCULATION

Guideline of transthyretin-related hereditary amyloidosis for clinicians

(2013) Yukio Ando et al.   Orphanet Journal of Rare Diseases

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

Consensus statement on the definition of orthostatic hypotension, neurally mediated syncope and the postural tachycardia syndrome

(2011) Roy Freeman et al.   AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL

Carpal tunnel syndrome as an initial manifestation in a case of transthyretin-related familial amyloid polyneuropathy with a novel A120T mutation

(2011) S. Koyama et al.   CLINICAL NEUROLOGY AND NEUROSURGERY

Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathy

(2010) Kana Tojo et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

Transthyretin-related amyloidoses and the heart: a clinical overview

(2010) Claudio Rapezzi et al.   Nature Reviews Cardiology

Recommendations for the Evaluation of Left Ventricular Diastolic Function by Echocardiography

(2009) S. F. Nagueh et al.   European Journal of Echocardiography