Cutaneous nerve biomarkers in transthyretin familial amyloid polyneuropathy

Author:

Ebenezer Gigi J.1,Liu Ying1,Judge Daniel P.2,Cunningham Kelly1,Truelove Shaun3,Carter Noel D.1,Sebastian Blessan1,Byrnes Kelly1,Polydefkis Michael1

Affiliation:

1. Department of Neurology; Johns Hopkins University

2. Division of Cardiology; Johns Hopkins University

3. Department of Epidemiology; Johns Hopkins Bloomberg School of Public Health; Baltimore MD

Funder

Pfizer

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference44 articles.

1. Familial amyloid polyneuropathy;Plante-Bordeneuve;Lancet Neurol,2011

2. Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey);Maurer;J Am Coll Cardiol,2016

3. Cardiac findings and events observed in an open-label clinical trial of tafamidis in patients with non-Val30Met and non-Val122Ile hereditary transthyretin amyloidosis;Damy;J Cardiovasc Transl Res,2015

4. Transthyretin cardiac amyloidosis: pathogenesis, treatments, and emerging role in heart failure with preserved ejection fraction;Ton;Clin Med Insights Cardiol,2014

5. Rapid progression of familial amyloidotic polyneuropathy: a multinational natural history study;Adams;Neurology,2015

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