Normal hemostatic parameters in children and young adults with α-thalassemia diseases
© 2016 Elsevier Ltd Thalassemia intermedia (TI), a non-transfusion dependent thalassemia, is divided into α-thalassemia, such as HbH disease, and β-thalassemia diseases, such as HbE/β+ thromboembolism (TE) in TI has been mostly reported in β-thalassemia diseases with incidence rates of 3.9–29%. The...
Saved in:
Main Authors: | Nongnuch Sirachainan, Ampaiwan Chuansumrit, Praguywan Kadegasem, Werasak Sasanakul, Pakawan Wongwerawattanakoon, Lalita Mahaklan |
---|---|
Other Authors: | Mahidol University |
Format: | Article |
Published: |
2018
|
Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/41080 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Mahidol University |
Similar Items
-
Aspirin resistance in children and young adults with splenectomized thalassemia diseases
by: Nongnuch Sirachainan, et al.
Published: (2018) -
Increased endothelial activation in α-thalassemia disease
by: Pankamol Sirivadhanakul, et al.
Published: (2020) -
The Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia
by: Ampaiwan Chuansumrit, et al.
Published: (2020) -
Combined chelation therapy with daily oral deferiprone and twice-weekly subcutaneous infusion of desferrioxamine in children with β-thalassemia: 3-year experience
by: Duantida Songdej, et al.
Published: (2018) -
New mathematical formula for differentiating thalassemia trait and iron deficiency anemia in thalassemia prevalent area: A study in healthy school-age children
by: Nongnuch Sirachainan, et al.
Published: (2018)