K. Kongthai

Association of Hb Shenyang [α26(B7)Ala→Glu, GCG>GAG, HBA2: c.80C>A (or HBA1)] with Several Types of α-Thalassemia in Thailand

S. Panyasai, Amphai Phasit, K. Kongthai, 2020, Hemoglobin.

A Formula to Identify Potential Cases of β-Thalassemia/HbE Disease Among Patients With Absent HbA, HbE >75% and HbF Between 5 and 15.

Manoo Punyamung, S. Pornprasert, Monthathip Tookjai, 2018, Laboratory medicine.

Detection of beta-thalassemia/hemoglobin E disease in samples which initially were diagnosed as homozygous hemoglobin E.

Y. Hattori, S. Pornprasert, J. Waneesorn, 2013, Clinical laboratory.

Detection of the common South-East Asian β0-thalassemia mutations in samples with borderline HbA2 levels

S. Pornprasert, K. Kongthai, Pitchaporn Rungsee, 2017, Clinical chemistry and laboratory medicine.

Comparison of HbA2, E, F and Red Cell Parameters in Homozygous HbE With and Without &agr;0-Thalassemia Trait

S. Pornprasert, Somkhid Thichak, Chaowanee Wangchauy, 2018, Laboratory medicine.

Quantification of hemoglobin Constant Spring in heterozygote and homozygote by a capillary electrophoresis method

P. Singboottra, S. Pornprasert, J. Waneesorn, 2012, International journal of laboratory hematology.

Comparison Between Capillary Electrophoresis and High Performance Liquid Chromatography for Detection and Quantification of Hb Constant Spring [Hb CS; α142, Term→Gln (TAA>CAA IN α2)]

P. Singboottra, S. Pornprasert, J. Waneesorn, 2011, Hemoglobin.