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Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|April 1, 2015
Detection of compound heterozygous of hb constant spring and hb q-Thailand by capillary electrophoresis and high performance liquid chromatographySakorn Pornprasert, Manoo PunyamungClinical Laboratory|January 14, 2014
Criteria for detection of alpha-thalassemia-1 Thai type deletion in routine laboratorySakorn Pornprasert, Manoo Punyamung, Kallayanee TreesuwanHemoglobin|April 18, 2015
Detection of Hb Constant Spring (HBA2: c.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb E Trait by Capillary ElectrophoresisSakorn Pornprasert, Supansa Saoboontan, Manoo PunyamungIndian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|July 21, 2025
Alpha-Thalassemia Caused by ααIVSI-1(AGGT> AGAT) (HBA1: c.95 + 1G > A) Mutation and its Combinations with Other Forms of Thalassemia or Hemoglobinopathy in Northern ThailandSakorn Pornprasert, Chedtapak Ruengdit, Manoo Punyamung, et al.Plos One|November 6, 2023
Single-tube multiplex real-time PCR with EvaGreen and high-resolution melting analysis for diagnosis of α0-thalassemia--SEA,--THAI, and--CR type deletionsChedtapak Ruengdit, Manoo Punyamung, Nutjeera Intasai, et al.Laboratory Medicine|September 22, 2018
A Formula to Identify Potential Cases of β-Thalassemia/HbE Disease Among Patients With Absent HbA, HbE >75% and HbF Between 5 and 15Sakorn Pornprasert, Monthathip Tookjai, Manoo Punyamung, et al.Hemoglobin|May 9, 2012
Hb 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, et al.Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|October 30, 2018
HbE Level and Red Cell Parameters in Heterozygous HbE With and Without α0-Thalassemia TraitSakorn Pornprasert, Monthathip Tookjai, Manoo Punyamung, et al.Laboratory Medicine|May 14, 2026
Hemoglobin Hekinan II (HBA1:c.84G>T): an electrophoretically silent α-globin variant missed by routine screening in northern ThailandMoe Theingi, Chedtapak Ruengdit, Manoo Punyamung, et al.Clinical Chemistry and Laboratory Medicine|May 22, 2015
Development of hemoglobin typing control materials for laboratory investigation of thalassemia and hemoglobinopathiesSakorn Pornprasert, Monthathip Tookjai, Manoo Punyamung, et al.Pageof 3