The genetic heterogeneity of hereditary transthyretin amyloidosis in a sample of the Brazilian population

Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe

(2016) Yesim Parman et al.   CURRENT OPINION IN NEUROLOGY

Genotype and Phenotype of Transthyretin Cardiac Amyloidosis

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

A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK

(2015) A S Carr et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments

(2015) Yoshiki Sekijima   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Transthyretin Asp38Tyr: a new mutation associated to a late onset neuropathy

(2015) Carolina Lavigne Moreira et al.   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

Description of transthyretin S50A, S52P and G47A mutations in familial amyloidosis polyneuropathy

(2013) Alejandra González-Duarte et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

Guideline of transthyretin-related hereditary amyloidosis for clinicians

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

Structure-Based Analysis of A19D, a Variant of Transthyretin Involved in Familial Amyloid Cardiomyopathy

(2013) Priscila Ferreira et al.   PLoS One

Regional differences and similarities of familial amyloidotic polyneuropathy (FAP) presentation in Brazil

(2012) Márcia Waddington Cruz   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

Vitreal deposits in Val71Ala transthyretin amyloidosis

(2012) D. Suan et al.   INTERNAL MEDICINE JOURNAL

Clinical and electrophysiological correlates of TTRala71 amyloid neuropathy

(2010) Wilson Marques Jr et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

Penetrance estimation of TTR familial amyloid polyneuropathy (type I) in Brazilian families

(2009) M. A. C. Saporta et al.   EUROPEAN JOURNAL OF NEUROLOGY

On the Origin of the Transthyretin Val30Met Familial Amyloid Polyneuropathy

(2008) C. Zaros et al.   ANNALS OF HUMAN GENETICS