Factor analysis of hepcidin on cardiac iron overload and fibrosis among thalassemia major children
Abstract Background Cardiac iron overload is a common cause of death in thalassemia major and is associated with hepcidin, which is primary iron homeostasis. Therapeutics that could increase hepcidin levels or act as hepcidin agonists might help treat the abnormal iron absorption in individuals with...
Saved in:
Main Authors: | Syarif Rohimi (Author), Bambang Budi Siswanto (Author), Muchtaruddin Mansyur (Author), Djajadiman Gatot (Author), Ina Sutanto (Author), Jacub Pandelaki (Author), Amiliana M. Soesanto (Author), Teddy Ontoseno (Author) |
---|---|
Format: | Book |
Published: |
SpringerOpen,
2024-08-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Hepcidin levels, markers of iron overload, and liver damage in children with beta-thalassemia major
by: Indah Sari, et al.
Published: (2024) -
Hepcidin gene polymorphisms and iron overload in β-thalassemia major patients refractory to iron chelating therapy
by: Parinaz Zarghamian, et al.
Published: (2020) -
Study of Hepcidin Level in Samples of Iraqi Patients With Iron Overload and Iron Deficiency Disorders
by: Dahlia Nayeef AL-Saidi, et al.
Published: (2016) -
Liver iron overload and hepatic function in children with thalassemia major
by: Pustika Amalia Wahidiyat, et al.
Published: (2018) -
Hemostatic abnormalities in children with thalassemia major and liver iron overload
by: Pustika Amalia Wahidiyat, et al.
Published: (2018)