Cargando…
Use of Drugs for ATTRv Amyloidosis in the Real World: How Therapy Is Changing Survival in a Non-Endemic Area
Background: Over the past decade, three new drugs have been approved for the treatment of hereditary amyloid transthyretin (ATTRv) polyneuropathy. The aim of this work was to analyze whether current therapies prolong survival for patients affected by ATTRv amyloidosis. Methods: The study was conduct...
Autores principales: | Russo, Massimo, Gentile, Luca, Di Stefano, Vincenzo, Di Bella, Gianluca, Minutoli, Fabio, Toscano, Antonio, Brighina, Filippo, Vita, Giuseppe, Mazzeo, Anna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146901/ https://www.ncbi.nlm.nih.gov/pubmed/33925301 http://dx.doi.org/10.3390/brainsci11050545 |
Ejemplares similares
-
Machine Learning for Early Diagnosis of ATTRv Amyloidosis in Non-Endemic Areas: A Multicenter Study from Italy
por: Di Stefano, Vincenzo, et al.
Publicado: (2023) -
Advances in Treatment of ATTRv Amyloidosis: State of the Art and Future Prospects
por: Russo, Massimo, et al.
Publicado: (2020) -
TTR-FAP: a single-center experience in Sicily, an Italian endemic area
por: Mazzeo, Anna, et al.
Publicado: (2015) -
Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP):
A Single-Center Experience in Sicily, an Italian Endemic Area
por: Mazzeo, Anna, et al.
Publicado: (2015) -
Is 99mTc-diphosphonate uptake the earliest sign of cardiac amyloidosis development in asymptomatic Glu89Gln transthyretin gene mutation carriers?
por: Minutoli, Fabio, et al.
Publicado: (2015)