Cargando…
Diagnostic challenges in hereditary transthyretin amyloidosis with polyneuropathy: avoiding misdiagnosis of a treatable hereditary neuropathy
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: | |
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 |
Ejemplares similares
-
Misdiagnoses of transthyretin amyloidosis: a clinical and electrodiagnostic study
por: Cortese, Andrea, et al.
Publicado: (2015) -
Lymphomatosis cerebri: a treatable cause of rapidly progressive dementia
por: Samani, Amit, et al.
Publicado: (2015) -
Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10
por: Carosi, Laura, et al.
Publicado: (2015) -
An n-of-one RCT for intravenous immunoglobulin G for inflammation in hereditary neuropathy with liability to pressure palsy (HNPP)
por: Vrinten, Charlotte, et al.
Publicado: (2016) -
Respiratory support in a population-based ALS cohort: demographic, timing and survival determinants
por: Chio, Adriano, et al.
Publicado: (2022)