Diagnostic challenges in hereditary transthyretin amyloidosis with polyneuropathy: avoiding misdiagnosis of a treatable hereditary neuropathy

Detalles Bibliográficos
Autores principales: Cortese, Andrea, Vegezzi, Elisa, Lozza, Alessandro, Alfonsi, Enrico, Montini, Alessandra, Moglia, Arrigo, Merlini, Giampaolo, Obici, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of Neurology, Neurosurgery, and Psychiatry 2017
Materias:
PostScript
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529976/
https://www.ncbi.nlm.nih.gov/pubmed/28188196
http://dx.doi.org/10.1136/jnnp-2016-315262

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529976/
https://www.ncbi.nlm.nih.gov/pubmed/28188196
http://dx.doi.org/10.1136/jnnp-2016-315262

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