Guideline of transthyretin-related hereditary amyloidosis for clinicians

Transthyretin amyloidosis is a progressive and eventually fatal disease primarily characterized by sensory, motor, and autonomic neuropathy and/or cardiomyopathy. Given its phenotypic unpredictability and variability, transthyretin amyloidosis can be difficult to recognize and manage. Misdiagnosis i...

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Bibliographic Details
Main Author: Ando, Y. (author)
Other Authors: Coelho, T. (author), Berk, J. (author), Cruz, M. (author), Ericzon, B. (author), Ikeda, S. (author), Lewis, W. (author), Obici, L. (author), Planté-Bordeneuve, V. (author), Rapezzi, C. (author), Said, G. (author), Salvi, F. (author)
Format: article
Language:eng
Published: 2014
Subjects:
Amyloidosis
Polyneuropathy
Cardiomyopathy
Oculoleptomeningeal
Transthyretin
Liver transplant
Genetics
Online Access:http://hdl.handle.net/10400.16/1608
Country:Portugal
Oai:oai:repositorio.chporto.pt:10400.16/1608

Internet

http://hdl.handle.net/10400.16/1608

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