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pro vyhledávání: '"Hisham Jeadi"'
Autor:
Hussam Ghoti, Hala Zreid, Israa Ghoti, Arno R. Bourgonje, Arjan Diepstra, Harry van Goor, Irit Avivi, Hisham Jeadi, Larissa E. van Eijk, Günter Weiss
Publikováno v:
EClinicalMedicine, Vol 62, Iss , Pp 102096- (2023)
Summary: Background: COVID-19 has raised special concern for patients with β-thalassemia major (β-TM) due to frequent comorbidities, regular blood transfusions, and iron overload. However, the exact implications of COVID-19 for patients with β-TM
Externí odkaz:
https://doaj.org/article/55f8d4bd1f9b40e68e2be81d9883a3f7
Publikováno v:
Hemoglobin. 41(2)
β-Thalassemia (β-thal) is a very common disease in the Palestinian population of the Gaza Strip. We studied their mutation frequency and clinical features. Thirteen different mutations were identified. The most common mutation was IVS-I-1 (G>A) (HB