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Hemoglobin|July 30, 2002
Compound heterozygosity for alpha0-thalassemia (- -THAI) and Hb constant spring causes severe Hb H diseaseVip Viprakasit, Voravarn S TanphaichitrThe Journal of Pediatrics|March 6, 2004
Unusual phenotype of hemoglobin EE with hemoglobin H disease: a pitfall in clinical diagnosis and genetic counselingVip Viprakasit, Voravarn S TanphaichitrThe Southeast Asian Journal of Tropical Medicine and Public Health|October 22, 2009
Rapid flow cytometric test using eosin-5-maleimide for diagnosis of red blood cell membrane disordersKalaya Tachavanich, Voravarn S Tanphaichitr, Wiyakan Utto, et al.Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|October 31, 2002
Early detection of cardiac involvement in beta-thalassemia childrenKritvikrom Durongpisitkul, Siwiluck Kruasukon, Charuwan Kangkagate, et al.Hemoglobin|August 25, 2005
A rare association of alphaO-thalassemia (--SEA) and an initiation codon mutation (ATG-->A-G) of the alpha2 gene causes Hb H disease in ThailandVip Viprakasit, Worrawut Chinchang, Waraporn Glomglao, et al.Hematology (Amsterdam, Netherlands)|June 19, 2004
Identification of Hb Q-India (alpha64 Asp-->His) in ThailandVip Viprakasit, Worrawut Chinchang, Parichat Pung-Amritt, et al.Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|October 31, 2002
Secondary hemophagocytic lymphohistiocytosis in children: an analysis of etiology and outcomeGavivann Veerakul, Kleebsabai Sanpakit, Voravarn S Tanphaichitr, et al.Journal of Pediatric Hematology/Oncology|March 7, 2003
Homozygous hemoglobin Tak causes symptomatic secondary polycythemia in a Thai boyVoravarn S Tanphaichitr, Vip Viprakasit, Gavivann Veerakul, et al.The Southeast Asian Journal of Tropical Medicine and Public Health|April 14, 2006
Validation of osmotic fragility test and dichlorophenol indophenol precipitation test for screening of thalassemia and Hb ESiripakorn Sangkitporn, Somchai Sangkitporn, Areerat Sangnoi, et al.Annals of Hematology|February 9, 2011
Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok NoiVoravarn S Tanphaichitr, Akira Hirono, Parichat Pung-amritt, et al.Pageof 3