Showing results (61-70 of 155) with videos related to

Sort By:
Pageof 16
The Southeast Asian Journal of Tropical Medicine and Public Health|March 28, 2009
Development of a comprehensive red blood cell enzymopathy laboratory in Thailand: the study of normal activity in eight erythroenzymes in ThaisKalaya Tachavanich, Vip Viprakasit, Parichat Pung-Amritt, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|August 30, 2005
Argininosuccinate synthetase deficiency: mutation analysis in 3 Thai patientsPornswan Wasant, Vip Viprakasit, Chantragan Srisomsap, et al.
Annals of Clinical Biochemistry|August 1, 2013
Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spotsPunyanuch Jindatanmanusan, Suchada Riolueang, Waraporn Glomglao, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|March 28, 2009
Clinical and hematological phenotype of homozygous hemoglobin E: revisit of a benign condition with hidden reproductive riskKalaya Tachavanich, Vip Viprakasit, Worawut Chinchang, et al.
International Journal of Cardiology|July 10, 2017
Detection of cardiac iron overload with native magnetic resonance T1 and T2 mapping in patients with thalassemiaRungroj Krittayaphong, Shuo Zhang, Pairash Saiviroonporn, et al.
Blood|January 13, 2004
Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemiaVip Viprakasit, Voravarn S Tanphaichitr, Worrawut Chinchang, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|May 12, 2012
Inter-site validations of the Pixel-Wise method for cardiac T2* analysis in transfusion-dependent Thai thalassemia patientsPairash Saiviroonporn, Vip Viprakasit, Adisak Maneesai, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|July 22, 2006
Dengue hemorrhagic fever in patients with thalassemiaBunchoo Pongtanakul, Nattee Narkbunnam, Gavivann Veerakul, et al.
British Journal of Haematology|March 5, 2003
De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemiaVip Viprakasit, Alexa M J Kidd, Helena Ayyub, et al.
Pageof 16