Zobrazeno 1 - 10
of 874
pro vyhledávání: '"Major Beta-Thalassemia"'
Autor:
Carsote, Mara1 (AUTHOR) carsote_m@hotmail.com, Vasiliu, Cristina2 (AUTHOR), Trandafir, Alexandra Ioana3 (AUTHOR), Albu, Simona Elena2 (AUTHOR), Dumitrascu, Mihai-Cristian2 (AUTHOR) carsote_m@hotmail.com, Popa, Adelina4 (AUTHOR), Mehedintu, Claudia5 (AUTHOR), Petca, Razvan-Cosmin6 (AUTHOR), Petca, Aida2 (AUTHOR), Sandru, Florica4 (AUTHOR)
Publikováno v:
Diagnostics (2075-4418). Aug2022, Vol. 12 Issue 8, p1921-N.PAG. 29p.
Autor:
Mohammadreza Rafati, Hossein Karami, Bita Lashtoo-Aghaee, Bahareh Lashtoo-Aghaee, Mojdeh Dabirian, Razieh Avan
Publikováno v:
Caspian Journal of Internal Medicine, Vol 13, Iss 1, Pp 61-69 (2022)
Background: Beta-thalassemia major patients typically require chronic transfusion and iron-chelating agents to reduce serum iron overload. Osveral® is an available Iranian brand name of deferasirox used by majority of thalassemic patients. The aim o
Externí odkaz:
https://doaj.org/article/23b091471b5d41bfb74bfc4191fcc45a
Akademický článek
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Autor:
Maaloul, I., Laaroussi, O., Jedidi, I., Sfaihi, L., Kmiha, S., Kamoun, T., Aloulou, H., Hachicha, M.
Publikováno v:
In Transfusion clinique et biologique February 2018 25(1):14-18
Publikováno v:
Journal of Tropical Life Science, Vol 6, Iss 1, Pp 10-14 (2016)
Major beta thalassemia (MBT) is a hereditary disease which synthesies defects in beta chains of haemoglobin, it is causes red blood cell destruction and the symptoms of anemia. Red blood cell destruction, frequent blood transfusion and low adherence
Externí odkaz:
https://doaj.org/article/48c570cf7b024b4796f2d888ab6853eb
Autor:
Riyanti, Eriska1, Achmad, Muhammad Harun2 harunachmader@gmail.com, Safari, Mieke Hemiawati3, Gartika, Meirina1, Ramadhany, Yunita Feby4
Publikováno v:
Systematic Reviews in Pharmacy. 2020, Vol. 11 Issue 4, p268-274. 7p. 6 Charts.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Mara Carsote, Cristina Vasiliu, Alexandra Ioana Trandafir, Simona Elena Albu, Mihai-Cristian Dumitrascu, Adelina Popa, Claudia Mehedintu, Razvan-Cosmin Petca, Aida Petca, Florica Sandru
Publikováno v:
Diagnostics, Vol 12, Iss 8, p 1921 (2022)
Beta-thalassemia (BTH), a recessively inherited haemoglobin (Hb) disorder, causes iron overload (IO), extra-medullary haematopoiesis and bone marrow expansion with major clinical impact. The main objective of this review is to address endocrine compo
Externí odkaz:
https://doaj.org/article/bbcfaaa875284180a776d6dec9360cf1
Autor:
Shahramian, I.1, Noori, N. M.2 dr_noori_cardio@yahoo.com, Teimouri, A.3, Akhlaghi, E.4, Sharafi, E.5
Publikováno v:
Iranian Journal of Pediatric Hematology & Oncology. 2015, Vol. 5 Issue 1, p11-17. 7p.
Publikováno v:
Journal of Agromedicine and Medical Sciences (AMS), Vol 4, Iss 1, Pp 18-24 (2018)
Repeated blood transfusions in patient with Major Beta Thalassemia leads to iron overload marks by the increased of serum ferritin levels. Free iron caused the change of H2O2 to oxidants by fenton reaction and caused oxidative stress. These oxidants
Externí odkaz:
https://doaj.org/article/ccd4dca5dd12484cad1be89af18a40a8