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Stem Cell Research|January 4, 2019
An integration-free iPSC line (MUSIi008-A) derived from a patient with severe hemolytic anemia carrying compound heterozygote mutations in KLF1 gene for disease modelingPonthip Potirat, Methichit Wattanapanitch, Vip Viprakasit, et al.
Scientific Reports|June 25, 2021
An urgent need for improving thalassemia care due to the wide gap in current real-life practice and clinical practice guidelinesSupachai Ekwattanakit, Chattree Hantaweepant, Archrob Khuhapinant, et al.
Advances in Hematology|October 11, 2012
Association of xmn I polymorphism and hemoglobin e haplotypes on postnatal gamma globin gene expression in homozygous hemoglobin eSupachai Ekwattanakit, Yuwarat Monteerarat, Suchada Riolueang, et al.
Journal of Pediatric Hematology/Oncology|March 7, 2003
Homozygous hemoglobin Tak causes symptomatic secondary polycythemia in a Thai boyVoravarn S Tanphaichitr, Vip Viprakasit, Gavivann Veerakul, et al.
Hemoglobin|October 31, 2002
Hb G-Makassar [beta6(A3)Glu-->Ala; codon 6 (GAG-->GCG)]: molecular characterization, clinical, and hematological effectsVip Viprakasit, Aranya Wiriyasateinkul, Benjamas Sattayasevana, et al.
The Cochrane Database of Systematic Reviews|November 2, 2016
Hydroxyurea for reducing blood transfusion in non-transfusion dependent beta thalassaemiasWai Cheng Foong, Jacqueline J Ho, C Khai Loh, et al.
British Journal of Haematology|May 25, 2002
Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of alpha thalassaemia (--MED/(alpha)TSaudi(alpha))Vip Viprakasit, Sarah Green, Sue Height, et al.
Hematology/Oncology and Stem Cell Therapy|July 26, 2012
Intersite validations of the pixel-wise method for liver R2* analysis in transfusion-dependent thalassemia patients: a more accessible and affordable diagnostic technologyPairash Saiviroonporn, Vip Viprakasit, Kleebsabai Sanpakit, et al.
American Journal of Hematology|March 12, 2013
Treating iron overload in patients with non-transfusion-dependent thalassemiaAli T Taher, Vip Viprakasit, Khaled M Musallam, et al.
Blood Reviews|February 20, 2018
A paradigm shift on beta-thalassaemia treatment: How will we manage this old disease with new therapies?Maria Domenica Cappellini, John B Porter, Vip Viprakasit, et al.
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