eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | thalassemia |
| Comorbidity | C0019196|hepatitis c |
| Sentences | 9 |
| PubMedID- 23414443 | Natural history of hepatitis c in thalassemia major: a long-term prospective study. |
| PubMedID- 23082485 | Hepcidin levels and iron status in beta-thalassemia major patients with hepatitis c virus infection. |
| PubMedID- 23412560 | hepatitis c in patients with beta-thalassemia major. |
| PubMedID- 24282420 | The prevalence of chronic hepatitis c infection in patients with beta thalassemia major is 18%, particularly because of blood transfusion before hcv serological testing (1, 5). |
| PubMedID- 23293194 | Conclusion: young beta thalassemia patients with active hepatitis c infection may have hepatic cirrhosis or fibrosis at young age when accompanied with hepatic siderosis. |
| PubMedID- 22180419 | Il28b polymorphisms influence stage of fibrosis and spontaneous or interferon-induced viral clearance in thalassemia patients with hepatitis c virus infection. |
| PubMedID- 21845061 | Effect of hepatic iron concentration and viral factors in chronic hepatitis c-infected patients with thalassemia major, treated with interferon and ribavirin. |
| PubMedID- 23489382 | Transient elastography in hepatitis c virus-infected patients with beta-thalassemia for assessment of fibrosis. |
| PubMedID- 22500658 | The incidence of hepatitis c in patients with thalassemia after screening in blood transfusion centers: a fourteen-year study. |
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