Zobrazeno 1 - 10
of 45
pro vyhledávání: '"major ß-thalassemia"'
Autor:
R Salah Noori, M Abdul-RedhaIsmaiel
Publikováno v:
Archives of Razi Institute, Vol 77, Iss 1, Pp 187-198 (2022)
Reduction or total lack of beta-globin chains caused by a congenital disease called ß-thalassemia major is one of the lives threatening diseases. Patients who suffer from ß-thalassemia need a repeated blood transfusion for survival. The repeated bl
Externí odkaz:
https://doaj.org/article/c0c12aba63604a7a81cd5c78f60f9d93
Autor:
Davarani, Esmat Rezabeigi1, Takaloo, Fatemeh Mohseni2, Vahidnia, Azar1, Daneshi, Salman3, Davarani, Maryam Rezabeigi4, Khanjani, Narges5, Hushmandi, Kiavash6, Raei, Mehdi7
Publikováno v:
Archives of Hygiene Sciences. Autumn2020, Vol. 9 Issue 4, p265-274. 10p.
Autor:
Salah Noori R; College of Science for Women, University of Babylon, Babylon, Iraq., Abdul-RedhaIsmaiel M; College of Science for Women, University of Babylon, Babylon, Iraq.
Publikováno v:
Archives of Razi Institute [Arch Razi Inst] 2022 Feb 28; Vol. 77 (1), pp. 187-198. Date of Electronic Publication: 2022 Feb 28 (Print Publication: 2022).
Autor:
Hashemi, A.1, Ordooei, M.1, Golestan, M.2, Akhavan Ghalifaf, M.3, Mahmoudabadi, F.3, Arefinia, M.3, Amanat, M.3, Purshamsi, F.3, Afkhami, M.3
Publikováno v:
Iranian Journal of Pediatric Hematology & Oncology. Mar2012, Vol. 2 Issue 1, p53-56. 4p.
Autor:
R, Salah Noori, M, Abdul-RedhaIsmaiel
Publikováno v:
Arch Razi Inst
Reduction or total lack of beta-globin chains caused by a congenital disease called ß-thalassemia major is one of the lives threatening diseases. Patients who suffer from ß-thalassemia need a repeated blood transfusion for survival. The repeated bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c4d45204d57fcf96f302e8839fe5665
https://pubmed.ncbi.nlm.nih.gov/35891728
https://pubmed.ncbi.nlm.nih.gov/35891728
Autor:
Javad Ghaffari, Koorosh Vahidshahi, Mehrnoosh Kosaryan, Zahra Soltantooyeh, Mohadese Mohamadi
Publikováno v:
Medicinski Glasnik, Vol 8, Iss 2, Pp 192-196 (2011)
Aim To investigate the humeral immune markers in patients with ß-thalassemia major (TM). Methods In this historical – cohort study (August to December 2007), the case group consisted of 34 TM patients and the control group included the same number
Externí odkaz:
https://doaj.org/article/48076e080434455c803425d1c8727aa3
Autor:
Shafiei, Alireza1, Kajiyazdi, Mohammad2, Ehsani, Mohammadali2, Shahgholi, Elham2, Aghabekloo, Saman3 saman.beglou@gmail.com
Publikováno v:
Journal of Clinical & Basic Research. 2022, Vol. 6 Issue 2, p21-28. 8p.
Publikováno v:
Polycyclic Aromatic Compounds. 2023, Vol. 43 Issue 3, p2770-2787. 18p.
Autor:
KARAKAŞ, Zeynep1 zeynepkar@hotmail.com, YILMAZ, Yasin1,2, ÇELİK, Dolay Damla3, ANNAYEV, Agageldi4, KURUCA, Serap ERDEM3
Publikováno v:
Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi. 2020, Vol. 83 Issue 4, p373-377. 5p.
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 1 (2014)
Patients with major ß-thalassemia require multi-transfusions for survival. They are at a high risk for blood transfusion transmitted infections, particularly with Hepatitis B virus (HBV), Hepatitis C virus (HCV) and Human immunodeficiency virus (HIV
Externí odkaz:
https://doaj.org/article/d73351e108a94e82ade1914f9c35a3a9