[HTML][HTML] Challenges of Iron Chelation in Thalassemic Children
A Adramerina, M Economou - Thalassemia Reports, 2024 - mdpi.com
Thalassemia treatment still relies on supportive care, mainly including blood transfusion and
iron chelation therapy. Iron chelation is considered the main factor responsible for the …
iron chelation therapy. Iron chelation is considered the main factor responsible for the …
[PDF][PDF] Iron Chelators in The Management of Hereditary Hemochromatosis
FU Onuigwe, RA Odeh, NJ Uchechukwu… - Elite Journal of …, 2024 - kiu.ac.ug
Hereditary Hemochromatosis (HH) is a genetic disorder characterized by abnormal iron
metabolism, leading to excessive iron absorption and deposition in various organs. This iron …
metabolism, leading to excessive iron absorption and deposition in various organs. This iron …
A Study of Serum Levels of Ferritin, Hepatic and Renal functions in Beta-Thalassemia Major (BTM) Patients Treated With Deferasirox (DFX) Tablets, Desferioxamine …
SM Mekkey, MA Ameen… - Al-Mustaqbal Journal of …, 2024 - mjpms.uomus.edu.iq
A category of inherited blood illnesses known as beta-thalassemias are defined by
abnormalities in the synthesis of hemoglobin beta chains, which can result in a wide range …
abnormalities in the synthesis of hemoglobin beta chains, which can result in a wide range …
Μεταβολικό προφίλ ετεροζυγωτών β-θαλασσαιμίας στον πληθυσμό της Χαλκιδικής
Μ Παπαγεωργίου - repo.lib.duth.gr
Περίληψη Η παρούσα μεταπτυχιακή διπλωματική εργασία επικεντρώνεται στην μελέτη της
θαλασσαιμίας και τον τρόπο που αυτή επηρεάζει το μεταβολικό προφίλ ετεροζυγωτών …
θαλασσαιμίας και τον τρόπο που αυτή επηρεάζει το μεταβολικό προφίλ ετεροζυγωτών …