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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| 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 |