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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Detalhes bibliográficos
Autor principal: Ando, Y. (author)
Outros Autores: 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)
Formato: article
Idioma:eng
Publicado em: 2014
Assuntos:
Amyloidosis
Polyneuropathy
Cardiomyopathy
Oculoleptomeningeal
Transthyretin
Liver transplant
Genetics
Texto completo:http://hdl.handle.net/10400.16/1608
País:Portugal
Oai:oai:repositorio.chporto.pt:10400.16/1608

Texto Completo

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

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