K. Torcharus

发表

Deferiprone (GPO‐L‐ONE®) monotherapy reduces iron overload in transfusion‐dependent thalassemias: 1‐year results from a multicenter prospective, single arm, open label, dose escalating phase III pediatric study (GPO‐L‐ONE; A001) from Thailand

Prapat Suriyaphol, A. Chuansumrit, J. Pooliam, 2013, American journal of hematology.

Moyamoya disease and protein S deficiency: a case report.

J. Laothamatas, K. Torcharus, A. Charuvanij, 1997, Pediatric neurology.

Red blood cell alloimmunization and other transfusion‐related complications in patients with transfusion‐dependent thalassemia: A multi‐center study in Thailand

P. Charoenkwan, A. Tantiworawit, P. Surapolchai, 2022, Transfusion.

Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots

V. Viprakasit, S. Chamnanvanakij, Punyanuch Jindatanmanusan, 2014, Annals of clinical biochemistry.

Original article. Efficacy of intravenous dexamethasone for the prevention of vomiting associated with intrathecal chemotherapy and ketamine sedation in children: a randomized, double-blinded, crossover, placebocontrolled trial

S. Charuluxananan, C. Traivaree, C. Komoltri, 2011 .

Factors affecting health-related quality of life in Thai children with thalassemia

K. Indaratna, A. Riewpaiboon, I. Nuchprayoon, 2010, BMC blood disorders.

Economic burden of beta-thalassemia/Hb E and beta-thalassemia major in Thai children

K. Indaratna, A. Riewpaiboon, I. Nuchprayoon, 2010, BMC Research Notes.

Effect of different transfusion regimens on craniofacial appearance and dentition in severe thalassemic children.

K. Torcharus, Varangkanar Jirarattanasopa, Phakatiti Hooncharoen, 2009, The Southeast Asian journal of tropical medicine and public health.

High transfusion in children with beta-thalassemia/Hb E: clinical and laboratory assessment of 18 cases.

T. Sriphaisal, P. Arnutti, K. Torcharus, 1993, Southeast Asian Journal of Tropical Medicine and Public Health.

Use of the gel test to follow up chimerism in ABO mismatched bone marrow transplantation patient: a case report.

O. Nathalang, T. Sriphaisal, P. Arnutti, 2005, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Health-related quality of life in Thai thalassemic children treated with iron chelation.

K. Torcharus, Tidarat Pankaew, 2011, The Southeast Asian journal of tropical medicine and public health.

Deferiprone (GPO‐L‐ONE®) monotherapy reduces iron overload in transfusion‐dependent thalassemias: 1‐year results from a multicenter prospective, single arm, open label, dose escalating phase III pediatric study (GPO‐L‐ONE; A001) from Thailand

A. Chuansumrit, J. Pooliam, S. Srichairatanakool, 2013, American journal of hematology.