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Results 1-10 of 11 (Search time: 0.001 seconds).
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Issue DateTitleAuthor(s)
1-Jan-2014Red cell indices and formulas used in differentiation of β-thalassemia trait from iron deficiency in Thai school childrenSakorn Pornprasert; Auttapon Panya; Manoo Punyamung; Jintana Yanola; Chatpat Kongpan
1-Aug-2012Hb A2/E levels found in co-inheritance with the α-thalassemia-1- SEA/ type deletion and either Hb e or β-thalassemiaSakorn Pornprasert; Kallayanee Treesuwan; Manoo Punyamung; Kunyakan Kongthai
1-Jan-2016Development of hemoglobin typing control materials for laboratory investigation of thalassemia and hemoglobinopathiesSakorn Pornprasert; Monthathip Tookjai; Manoo Punyamung; Panida Pongpunyayuen; Kanokwan Jaiping
28-Mar-2018Proficiency testing program for hemoglobin E, A<inf>2</inf>and F analysis in Thailand using lyophilized hemoglobin control materialsSakorn Pornprasert; Monthathip Tookjai; Manoo Punyamung; Panida Pongpunyayuen; Kallayanee Treesuwan
12-Mar-2018HbE Level and Red Cell Parameters in Heterozygous HbE With and Without α<sup>0</sup>-Thalassemia TraitSakorn Pornprasert; Monthathip Tookjai; Manoo Punyamung; Panida Pongpunyayuen
21-Mar-2018Hematological Analysis in Thai Samples with Deletional and Nondeletional HbH DiseasesSakorn Pornprasert; Nur Afsan Salaeh; Monthathip Tookjai; Manoo Punyamung; Panida Pongpunyayuen; Kallayanee Treesuwan
1-Jan-2015Detection of Hb Constant Spring (HBA2: C.427T&gt;C) Heterozygotes in Combination with β-Thalassemia or Hb e Trait by Capillary ElectrophoresisSakorn Pornprasert; Supansa Saoboontan; Manoo Punyamung
1-Jan-2015Red cell indices and formulas used in differentiation of β-thalassemia trait from iron deficiency in Thai AdultsSoontharee Plengsuree; Manoo Punyamung; Jintana Yanola; Siriporn Nanta; Kanokwan Jaiping; Kritsanee Maneewong; Sanchai Wongwiwatthananukit; Sakorn Pornprasert
1-Jun-2015Detection of Compound Heterozygous of Hb Constant Spring and Hb Q-Thailand by Capillary Electrophoresis and High Performance Liquid ChromatographySakorn Pornprasert; Manoo Punyamung
1-Jan-2019A formula to identify potential cases of β-thalassemia/HbE disease among patients with absent HbA, HbE &gt;75% and HbF between 5 and 15%Sakorn Pornprasert; Monthathip Tookjai; Manoo Punyamung; Kanyakan Kongthai