Hepatocellular carcinoma in adult thalassemia patients: an expert opinion based on current evidence

Beta-thalassemia represents a heterogeneous group of haemoglobin inherited disorders, among the most common genetic diseases in the world, frequent in the Mediterranean basin. As beta-thalassemia patients’ survival has increased over time, previously unknown complications are observed with increasin...

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Detalles Bibliográficos
Autores principales: Mangia, Alessandra, Bellini, Davide, Cillo, Umberto, Laghi, Andrea, Pelle, Giuseppe, Valori, Vanna Maria, Caturelli, Eugenio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398335/
https://www.ncbi.nlm.nih.gov/pubmed/32746786
http://dx.doi.org/10.1186/s12876-020-01391-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398335/
https://www.ncbi.nlm.nih.gov/pubmed/32746786
http://dx.doi.org/10.1186/s12876-020-01391-z

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