|1.||Fucharoen, Supan: 16 articles (01/2015 - 01/2002)|
|2.||Sanchaisuriya, Kanokwan: 15 articles (01/2015 - 01/2002)|
|3.||Fucharoen, Goonnapa: 15 articles (01/2015 - 01/2002)|
|4.||Li, Dong-Zhi: 5 articles (09/2013 - 01/2010)|
|5.||Liao, Can: 5 articles (09/2013 - 01/2007)|
|6.||Viprakasit, Vip: 4 articles (08/2015 - 02/2002)|
|7.||Li, Ru: 4 articles (09/2013 - 01/2010)|
|8.||Xie, Xing-Mei: 4 articles (09/2013 - 01/2010)|
|9.||Zhou, Jian-Ying: 4 articles (09/2013 - 01/2010)|
|10.||Fucharoen, S: 4 articles (10/2003 - 02/2001)|
04/01/2014 - "The study provides basic epidemiological information about Hb CS as well as other forms of thalassemia for a specific group of an ethnic minority in Vietnam. "
04/01/2015 - "Slightly decreased MCV and CH are suggestive of α-thalassemia 2, Hb CS, and Hb E heterozygotes whereas the increased Rbc counts are obvious in α-thalassemia 1 and β-thalassemia. "
01/01/2015 - "Hb CS is commonly found in combination with other thalassemias among Southeast Asian populations. "
01/01/2015 - "To evaluate the efficiency of Hb CS determination by HPLC, blood samples from 578 subjects were analyzed using an automated cell analyzer for hematological parameters, automated HPLC for Hb identification, and polymerase chain reaction (PCR) for α-thalassemia (α-thal) and Hb CS confirmation. "
01/01/2015 - "Detection of Hb Constant Spring (HBA2: c.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb E Trait by Capillary Electrophoresis."
06/01/2010 - "This study was aimed to establish a method of PCR combination with PCR-RFLP for detecting the South-East Asian (SEA) deletion type alpha-thalassemia 1 and non-deletion mutation of Hb Constant Spring (CS), and to investigate the application value of this method. "
12/01/2005 - "This study aims to determine the different types of deletional alpha-thalassemia and Hemoglobin Constant Spring (HbCS), and their frequency in Malays, Chinese and Indians in Malaysia. "
01/01/2015 - "There were 27 cases found as positive for alpha-thalassemia including alpha-thalassemia-1 carriers, South East Asian type, alpha-thalassemia-1 carriers, Thai deletion type, HbH and Hb constant spring, which were 18, 2, 3, and 2 cases, respectively. "
08/01/2010 - "Hemoglobin Constant Spring (HbCS) is the most common nondeletional alpha-thalassemia variant causing HbH disease, making its detection crucial in populations at risk. "
08/01/2010 - "Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional alpha-thalassemia mutations."
|3.||beta-Thalassemia (Cooley's Anemia)
08/01/2012 - "Beta-thalassemia trait also significantly decreased the expression of HbH, Hb Constant Spring when present, and HbA(2) , with levels as low as 3.6% on high-performance liquid chromatography (HPLC). "
04/15/2010 - "Hb CS-H disease combined with beta-thalassemia--a case report."
09/01/2007 - "Hematological findings confirm the mild thalassemia intermedia phenotypes for pure homozygous Hb CS and homozygous Hb CS with Hb E heterozygote and Hb E homozygote. "
09/01/2007 - "Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis."
11/01/2005 - "These cases included 5 cases of Hb H disease, 5 cases of Hb H with Hb Constant Spring (CS), 9 cases of beta-thalassemia/Hb E disease and 1 case of beta-thalassemia major. "
|4.||Hydrops Fetalis (Fetal Edema)
01/01/2015 - "Our study highlights the significance of watchful observation using a serial ultrasound method and care of pregnant women who have fetuses found to carry Hb H/Hb CS disease during pregnancy, to guard against the occurrence of fetal hydrops. "
01/01/2015 - "Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family."
01/01/2015 - "Here, we describe one case with Hb H/Hb CS disease that presented with fetal anemia and fetal hydrops, known as Hb H (β4) hydrops fetalis. "
06/15/2005 - "In a parallel study, P falciparum invasion was investigated in density-fractionated RBCs from healthy subjects and from individuals with inherited RBC abnormalities affecting primarily hemoglobin (Hb) or the RBC membrane (thalassemias, hereditary ovalocytosis, xerocytosis, Hb CC, and Hb CS). "
|4.||Hemoglobin Constant Spring
|5.||DNA (Deoxyribonucleic Acid)
|7.||hemoglobin Quong Sze
|9.||Terminator Codon (Termination Codon)
|10.||hemoglobin Q Thailand