- Effects of α-tocopherol on hemolysis and oxidative stress markers on red blood cells in β-thalassemia major
-
Sovira N, Lubis M, Wahidiyat PA, Suyatna FD, Gatot D, Bardosono S, Sadikin M
- KMID: 2504934
- Clin Exp Pediatr.
- 2020 Aug;63(8):314-320.
- doi: 10.3345/cep.2019.00542
Background: The accumulation of unpaired α-globin chains in patients with β-thalassemia major may clinically create ineffective erythropoiesis, hemolysis, and chronic anemia. Multiple blood transfusions and iron overload cause cellular oxidative... -
- CITED
-
- Close
- SHARE
-
- Close
- FVIII inhibitor surveillance in children with hemophilia A in Indonesia: a report from the Indonesian Pediatric Hematology-Oncology Working Group
-
Chozie NA, Gatot D, Sudarmanto B, Susanah S, Purnamasari R, Widjajanto PH, Nugroho S, Rasiyanti O, Puspitasari D, Riza M, Shanty Larasati MC, Adiyanti SS, Saraswati MC, Primacakti F, on behalf of the Pediatric Hematology-Oncology Working Group of the Indonesian Pediatric Society
- KMID: 2537550
- Blood Res.
- 2022 Dec;57(4):272-277.
- doi: 10.5045/br.2022.2022153
Background Factor VIII (FVIII) inhibitor diagnosis and surveillance in Indonesia are challenging owing to geographic conditions and the lack of laboratory facilities nationwide for inhibitor assays. This study aimed to determine... -
- CITED
-
- Close
- SHARE
-
- Close
