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Browsing by Author Worrawut Chinchang

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Showing results 1 to 10 of 10
Issue DateTitleAuthor(s)
1-Dec-2004Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constants Spring (Hb CS/CS): A case reportVip Viprakasit; Gavivann Veerakul; Kleebsabai Sanpakit; Bunchoo Pongtanakul; Worrawut Chinchang; Voravarn S. Tanphaichitr; Mahidol University
1-Aug-2005Clinical phenotypes and molecular diagnosis in a hitherto interaction of Hb E/β thalassemia syndrome (β<sup>E</sup>/ β<sup>-31, A→G</sup>)Nassawee Vathana; Vip Viprakasit; Kleebsabi Sanpakit; Worrawut Chinchang; Gavivann Veerakul; Voravarn Tanphaichitr; Mahidol University
1-Mar-2004Co-inheritance of Hb Pak Num Po, a Novel α1 Gene Mutation, and α<sup>0</sup>Thalassemia Associated with Transfusion-Dependent Hb H DiseaseVip Viprakasit; Voravarn S. Tanphaichitr; Gavivann Veerakul; Worrawut Chinchang; Siripan Petrarat; Parichat Pung-Amritt; Douglas R. Higgs; Mahidol University; University of Oxford; John Radcliffe Hospital
1-May-2004Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with β thalassemiaVip Viprakasit; Voravarn S. Tanphaichitr; Worrawut Chinchang; Pakarat Sangkla; Mitchell J. Weiss; Douglas R. Higgs; Mahidol University
1-Jan-2007Further identification of Hb G-Coushatta [β22(B4)Glu→Ala (GAA→GCA)] in Thailand by the polymerase chain reaction-single-strand conformation polymorphism technique and by amplification refractory mutation system-polymerase chain reactionWorrawut Chinchang; Vip Viprakasit; Mahidol University
1-Jan-2006Hb Woodville, a rare α-globin variant, caused by codon 6 mutation of the α1 geneVip Viprakasit; Worrawut Chinchang; Pipat Chotimarat; Mahidol University; Yala Hospital
1-Jan-2005Identification of the novel signal peptide mutation, antithrombin-Siriraj causes type-I antithrombin deficiency in Thai patientsYingyong Chinthammitr; Worrawut Chinchang; Theera Ruchutrakool; Vip Viprakasit; Mahidol University; Leiden University Medical Center - LUMC
1-Nov-2005Molecular analysis of unknown β-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with β-thalassemias and β-globin variantsWorrawut Chinchang; Vip Viprakasit; Parichat Pung-Amritt; Voravarn S. Tanphaichitr; Pa Thai Yenchitsomanus; Mahidol University
1-Jul-2004Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorderVip Viprakasit; Prin Vathesathokit; Worrawut Chinchang; Kalaya Tachavanich; Parichat Pung-Amritt; Victoria L.C. Wimhurst; Pa Thai Yenchitsomanus; Alison T. Merryweather-Clarke; Voravarn S. Tanphaichitr; Mahidol University; Weatherall Institute of Molecular Medicine
16-Aug-2005A rare association of α<sup>0</sup>-thalassemia (--<sup>SEA</sup>) and an initiation codon mutation (ATG→A-G) of the α2 gene causes Hb H disease in ThailandVip Viprakasit; Worrawut Chinchang; Waraporn Glomglao; Voravarn S. Tanphaichitr; Mahidol University