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Results 31-40 of 48 (Search time: 0.005 seconds).
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Issue DateTitleAuthor(s)
1-Oct-2010Diagnosis of thalassemia on dried blood spot samples by high performance liquid chromatographySakorn Pornprasert; Chutharat Kasemrad; Kanyakan Sukunthamala
1-Jul-2008Analysis of real-time SYBR-polymerase chain reaction cycle threshold for diagnosis of the α-thalassemia-1 Southeast Asian type deletion: Application to carrier screening and prenatal diagnosis of Hb Bart's hydrops fetalisSakorn Pornprasert; Kanyakan Sukunthamala; Jittraporn Sacome; Arunee Phusua; Rattika Saetung; Torpong Sanguansermsri; Pranee Leechanachai
2-Jan-2019A Case Report of Compound Heterozygosity for β<sup>0</sup>/β<sup>+</sup>-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'<inf>2</inf> SampleNutjeera Intasai; Ampai Phasit; Sitthichai Panyasai; Sakorn Pornprasert
1-Jan-2019Development of suitable external quality control material for G6PD deficiency screening with the fluorescent spot testNattasit Pienthai; Panida Pongpunyayuen; Chedtapak Ruengdit; Sakorn Pornprasert
3-Sep-2019Analysis of Deletional Hb H Diseases in Samples with Hb A<inf>2</inf>-Hb H and Hb A<inf>2</inf>-Hb Bart’s on Capillary ElectrophoresisKunyakan Khongthai; Chedtapak Ruengdit; Sitthichai Panyasai; Sakorn Pornprasert
1-Jan-2019False-positive result of immunochromatographic (IC) strip test for the diagnosis of α-thalassemia in samples with autoantibodiesPatcharapong Pantiya; Saowanit Chairatanapiwong; Dararat Dankai; Sarayut Nualkeaw; Kanokwan Jaiping; Panthong Singboottra; Sakorn Pornprasert
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
16-Jul-2019Validation of Microarray for the Simultaneous Detection of Common α- and β-Thalassemia Gene MutationsSakorn Pornprasert; Rinradee Anurak; Chedtapak Ruengdit; Nattasit Pienthai; Monthathip Tookjai; Manoo Punyamung; Panida Pongpunyayuen
1-Jan-2020Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation --<sup>SEA</sup>/--<sup>CR</sup>, a novel α<sup>0</sup>-thalassemia deletionChedtapak Ruengdit; Sitthichai Panyasai; Naowarat Kunyanone; Worawich Phornsiricharoenphant; Chumpol Ngamphiw; Sissades Tongsima; Orapan Sripichai; Serge Pissard; Sakorn Pornprasert
3-May-2020Association of Hb A<inf>2</inf> Variants with Several Forms of α- and β-Thalassemia in ThailandSitthichai Panyasai; Sakorn Pornprasert