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American Journal of Hematology|January 24, 2018
A prospective analysis for prevalence of complications in Thai nontransfusion-dependent Hb E/β-thalassemia and α-thalassemia (Hb H disease)Supachai Ekwattanakit, Noppadol Siritanaratkul, Vip Viprakasit
European Journal of Haematology|August 2, 2003
Dinucleotide deletion in -alpha3.7 allele causes a severe form of alpha+ thalassaemiaVip Viprakasit, Helena Ayyub, Alison May
European Journal of Haematology|December 14, 2005
Hb Woodville, a rare alpha-globin variant, caused by codon 6 mutation of the alpha1 geneVip Viprakasit, Worrawut Chinchang, Pipat Chotimarat
Mediterranean Journal of Hematology and Infectious Diseases|September 14, 2023
Justification of Universal Iron Supplementation for Infants 6-12 months in Regions with a High Prevalence of ThalassemiaPhakatip Sinlapamongkolkul, Pacharapan Surapolchai, Vip Viprakasit
British Journal of Haematology|March 21, 2014
Current approach to iron chelation in childrenYesim Aydinok, Antonis Kattamis, Vip Viprakasit
Genes|September 23, 2022
Common Single Nucleotide Polymorphism of TMPRSS6, an Iron Regulation Gene, Associated with Variable Red Blood Cell Indices in Deletional α-Globin GenotypesThidarat Suksangpleng, Waraporn Glomglao, Vip Viprakasit
Hematology (Amsterdam, Netherlands)|August 4, 2017
Interaction between Hb E and Hb Yala (HBB:c.129delT); a novel frameshift beta globin gene mutation, resulting in Hemoglobin E/β0 thalassemiaSupachai Ekwattanakit, Suchada Riolueang, Vip Viprakasit
Pediatric Blood & Cancer|June 2, 2022
Bone mineral density in primarily preadolescent children with hemoglobin E/β-thalassemia with different severities and transfusion requirementsPairunyar Nakavachara, Praewvarin Weerakulwattana, Julaporn Pooliam, et al.
Clinical and Translational Science|April 14, 2026
Thailand's Emerging Role in the Cell and Gene Therapy Revolution: A Review of Progress and PotentialVip Viprakasit, Warut Tulalamba, Thidarat Suksangpleng, et al.
Pediatric Blood & Cancer|December 27, 2019
Early development of decreased β-cell insulin secretion in children and adolescents with hemoglobin H disease and its relationship with levels of anemiaPairunyar Nakavachara, Worarat Kajchamaporn, Julaporn Pooliam, et al.
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