Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ebrahim Miri-Moghadam"'
Publikováno v:
Iranian Journal of Pathology, Vol 16, Iss 4, Pp 354-361 (2021)
Background & Objective: Epithelial-Mesenchymal transition (EMT) is known to be a possible mechanism in tumor progression; however, there is insufficient evidence to support the contribution of this process in human cancers. The present study aimed to
Externí odkaz:
https://doaj.org/article/bd60eed47b214ec98347c310d34227da
Publikováno v:
Annals of Global Health, Vol 87, Iss 1 (2021)
Background: Blood transfusion is a traditional treatment for β-thalassemia (β-thal) that improves the patients’ anemia and lifespan, but it may lead to iron overload in parenchymal tissue organs and endocrine glands that cause their dysfunctions
Externí odkaz:
https://doaj.org/article/523e3822da984ffb9f001b722ccd1583
Publikováno v:
Hemoglobin. 32(5)
In a recent study, we demonstrated that, in the Iranian province of Sistan-Baluchestan (S-B), the IVS-I-5 (GC) beta-thalassemia (beta-thal) mutation is highly prevalent. In the present article we report the hematological phenotype as measured in 289
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6903592965402af6b74edd1608b38958
https://pubmed.ncbi.nlm.nih.gov/18932068
https://pubmed.ncbi.nlm.nih.gov/18932068
Autor:
Peyman, Eshghi, Azita, Zadeh-Vakili, Armin, Rashidi, Ebrahim, Miri-Moghaddam, Ebrahim, Miri-Moghadam
Publikováno v:
Hemoglobin. 32(4)
Iran, a country located on the "thalassemia belt", is an area with an unusually high prevalence of beta-thalassemia (thal). The gene frequency of thalassemia shows great variation within Iran from one area to another. The purpose of this study was to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8137d645f5f8a815f45e2141160dcd9
https://pubmed.ncbi.nlm.nih.gov/18654889
https://pubmed.ncbi.nlm.nih.gov/18654889