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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | BMC Gastroenterol |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2020
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7398335/ https://ncbi.nlm.nih.gov/pubmed/32746786 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12876-020-01391-z |
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