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Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|April 27, 2026
Compound Heterozygosity for Hb Queens Park (α32(B13)Met→Lys) and α-thalassemia Found in Northern ThailandMoe Moe Paing, Chedtapak Ruengdit, Manoo Punyamung, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 21, 2022
Diagnosis of α0-thalassemia Chiang Rai (--CR) deletion by melt curve analysis in Northern ThailandChedtapak Ruengdit, Pinyaphat Khamphikham, Manoo Punyamung, et al.
Hemoglobin|July 3, 2014
Red cell indices and formulas used in differentiation of β-thalassemia trait from iron deficiency in Thai school childrenSakorn Pornprasert, Auttapon Panya, Manoo Punyamung, et al.
Hemoglobin|May 6, 2025
Characterization of HbH Disease Caused by Compound Heterozygotes α+-Thalassemia 3.7 kb Deletion and a Large Novel α0-Thalassemia DeletionChedtapak Ruengdit, Manoo Punyamung, Kritsanee Maneewong, et al.
Clinical Chemistry and Laboratory Medicine|November 28, 2017
Proficiency testing program for hemoglobin E, A2 and F analysis in Thailand using lyophilized hemoglobin control materialsSakorn Pornprasert, Monthathip Tookjai, Manoo Punyamung, et al.
Clinical Chemistry and Laboratory Medicine|January 10, 2024
A comparative evaluation of the analytical performances of premier resolution-high-performance liquid chromatography (PR-HPLC) with capillary zone electrophoresis (CZE) assays for the detection of hemoglobin variants and the quantitation of HbA0, A2, E, and FSirikwan Laksap, Suphisara Suanboon, Manoo Punyamung, et al.
Hemoglobin|February 10, 2022
Multiplex Quantitative Real-Time Polymerase Chain Reaction and High-Resolution Melting Analysis for Identification of a Couple At-Risk of Having a Newborn with Severe ThalassemiaChedtapak Ruengdit, Manoo Punyamung, Pinyaphat Khamphikham, et al.
Hemoglobin|May 26, 2020
Proficiency Testing Program for Hb E (HBB: c.79G>A) Screening in Thailand Using Lyophilized Hb E Control MaterialsSakorn Pornprasert, Sirithorn Surajinda, Panida Pongpunyayuen, et al.
Hemoglobin|August 23, 2024
The First Thai Case of Nondeletional HbH Disease Caused by Compound Heterozygosity for α-Thalassemia-1 Chiang Rai (--CR) Type Deletion with Hb Constant SpringDuantida Songdej, Praguywan Kadegasem, Nongnuch Sirachainan, et al.
Laboratory Medicine|January 19, 2018
Hematological Analysis in Thai Samples With Deletional and Nondeletional HbH DiseasesSakorn Pornprasert, Nur-Afsan Salaeh, Monthathip Tookjai, et al.
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