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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Dades bibliogràfiques
Autors principals: Ando, Yukio, Coelho, Teresa, Berk, John L, Cruz, Márcia Waddington, Ericzon, Bo-Göran, Ikeda, Shu-ichi, Lewis, W David, Obici, Laura, Planté-Bordeneuve, Violaine, Rapezzi, Claudio, Said, Gerard, Salvi, Fabrizio
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2013
Matèries:
Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3584981/
https://ncbi.nlm.nih.gov/pubmed/23425518
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-8-31
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