Citations (14)
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Read on this site (7)
Chedtapak Ruengdit, Manoo Punyamung, Pinyaphat Khamphikham, Panida Pongpunyayuen, Nutjeera Intasai & Sakorn Pornprasert. (2021) 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 Thalassemia. Hemoglobin 45:5, pages 309-313.
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Soontharee Plengsuree, Manoo Punyamung, Jintana Yanola, Siriporn Nanta, Kanokwan Jaiping, Kritsanee Maneewong, Sanchai Wongwiwatthananukit & Sakorn Pornprasert. (2015) Red Cell Indices and Formulas Used in Differentiation of β-Thalassemia Trait from Iron Deficiency in Thai Adults. Hemoglobin 39:4, pages 235-239.
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Sitthichai Panyasai, Kanokwan Jaiping & Sakorn Pornprasert. (2015) Elevated Hb A2 Levels in a Patient with a Compound Heterozygosity for the (β+) −31 (A > G) and (β0) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene. Hemoglobin 39:4, pages 292-295.
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Sakorn Pornprasert, Auttapon Panya, Manoo Punyamung, Jintana Yanola & Chatpat Kongpan. (2014) Red Cell Indices and Formulas Used in Differentiation of β-Thalassemia Trait from Iron Deficiency in Thai School Children. Hemoglobin 38:4, pages 258-261.
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Sakorn Pornprasert, Kallayanee Treesuwan, Manoo Punyamung & Kunyakan Kongthai. (2012) Hb A2/E Levels Found in Co-Inheritance with the α-Thalassemia-1 – –SEA/ Type Deletion and Either Hb E or β-Thalassemia. Hemoglobin 36:4, pages 381-387.
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Sakorn Pornprasert, Sitthichai Panyasai, Kanyakan Kongthai & Kallayanee Treesuwan. (2012) Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-Thalassemia Codon 17 (A>T) in a Thai Patient. Hemoglobin 36:3, pages 265-269.
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Sakorn Pornprasert, Chutharat Kasemrad & Kanyakan Sukunthamala. (2010) Diagnosis of Thalassemia on Dried Blood Spot Samples by High Performance Liquid Chromatography. Hemoglobin 34:5, pages 486-494.
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Articles from other publishers (7)
Chedtapak Ruengdit, Manoo Punyamung, Nutjeera Intasai & Sakorn Pornprasert. (2023) Single-tube multiplex real-time PCR with EvaGreen and high-resolution melting analysis for diagnosis of α0-thalassemia--SEA,--THAI, and--CR type deletions. PLOS ONE 18:11, pages e0293838.
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Pitchaporn Rungsee, Kanyakan Kongthai & Sakorn Pornprasert. (2017) Detection of the common South-East Asian β0-thalassemia mutations in samples with borderline HbA2 levels. Clinical Chemistry and Laboratory Medicine (CCLM) 55:1, pages e17-e20.
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Siew Leng Kho, Kek Heng Chua, Elizabeth George & Jin Ai Mary Anne Tan. (2015) A novel gap-PCR with high resolution melting analysis for the detection of α-thalassaemia Southeast Asian and Filipino β0-thalassaemia deletion. Scientific Reports 5:1.
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Watcharee Prasing & Sakorn Pornprasert. (2014)
Measurement of HbA
2
by Capillary Electrophoresis for Diagnosing β-thalassemia/HbE Disease in Patients With Low HbF
. Laboratory Medicine 45:3, pages 226-230.
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Sakorn Pornprasert, Thanatcha Wiengkum, Sarinee Srithep, Isarapong Chainoi, Panthong Singboottra & Sanchai Wongwiwatthananukit. (2011) Detection of α-thalassemia-1 Southeast Asian and Thai Type Deletions and β-thalassemia 3.5-kb Deletion by Single-tube Multiplex Real-time PCR with SYBR Green1 and High-resolution Melting Analysis. Annals of Laboratory Medicine 31:3, pages 138-142.
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Sitthichai Panyasai, Kanyakan Sukunthamala, Kanokwan Jaiping, Sanchai Wongwiwatthananukit, Panthong Singboottra & Sakorn Pornprasert. (2011) Interference of Hemoglobin Hope on β-Thalassemia Diagnosis by the Capillary Electrophoresis Method. American Journal of Clinical Pathology 136:1, pages 14-18.
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Sakorn Pornprasert & Kanyakan Sukunthamala. (2010) SYTO9 and SYBR GREEN1 with a high-resolution melting analysis for prenatal diagnosis of β0-thalassemia/hemoglobin-E. European Journal of Haematology 85:5, pages 424-429.
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