|1.||Chen, Zhizhong: 2 articles (11/2014 - 08/2014)|
|2.||Li, Youqiong: 2 articles (11/2014 - 08/2014)|
|3.||Qin, Guifang: 2 articles (11/2014 - 08/2014)|
|4.||Zhao, Lin: 2 articles (11/2014 - 08/2014)|
|5.||Xu, Xiangmin: 2 articles (03/2010 - 07/2008)|
|6.||Chhabra, Sanjeev: 1 article (02/2016)|
|7.||Das, Reena: 1 article (02/2016)|
|8.||Sharma, Aman: 1 article (02/2016)|
|9.||Kaur Sachdeva, Ravinder: 1 article (02/2016)|
|10.||Sharma, Prashant: 1 article (02/2016)|
|1.||beta-Thalassemia (Cooley's Anemia)
03/01/1977 - "Improved techniques in hemoglobin A2 quantification remain the best approach for detecting beta-thalassemia heterozygotes."
02/01/2016 - "Effect of antiretroviral therapy on hemoglobin A2 values can have implications in antenatal beta-thalassemia screening programs."
11/01/2010 - "Patients with beta-thalassemia trait usually have elevated levels of hemoglobin A2."
03/01/2010 - "Sandwich ELISA for hemoglobin A2 quantification and identification of beta-thalassemia carriers."
09/01/2008 - "Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of beta-thalassemia."
11/01/2000 - "Hemoglobin A2 (alpha2delta2), which is present at low concentration (1-2%) in the circulating red cells of normal individuals, has two important features that merit its study, i.e., it inhibits polymerization of sickle HbS and its elevated concentration in some thalassemias is a useful clinical diagnostic. "
10/01/2015 - "Automated high performance liquid chromatography and Capillary electrophoresis are used to quantitate the proportion of Hemoglobin A2 (HbA2 ) in blood samples order to enable screening and diagnosis of carriers of β-thalassemia. "
07/01/2015 - "We firstly established the link between KLF1 mutations and relatively elevated hemoglobin A2 (HbA2 ) and HbF levels, along with lower mean corpuscular volume (MCV) and mean corpuscular hemoglobin (MCH) values in a group of α-thalassemia carriers. "
01/01/2015 - "Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening."
11/01/2014 - "[Analysis of thalassemia gene profiling of hemoglobin A2 as 2.5%-3.5%]."
08/19/1980 - "Quantitation of hemoglobin A2 in alpha thalassemia trait by microcolumn chromatography."
09/01/2015 - "Hemoglobin A2 values in sickle cell disease patients quantified by high performance liquid chromatography and the influence of alpha thalassemia."
09/01/1995 - "Where there is microcytosis, normal values, together with normal hemoglobin A2 and serum ferritin concentrations, are likely to indicate alpha-thalassemia trait."
12/01/2010 - "The standard diagnostic marker for beta-thalassemia is elevation of the hemoglobin A2 (HbA2) level (>3·5%), while low mean corpuscular volume (MCV<80) and mean cell hemoglobin (MCH<27) with a normal HbA2 level indicate alpha-thalassemia carrier. "
02/01/2007 - "In Ontario, Canada, beta-thalassemia is easily detected through measurement of hemoglobin A2, but most laboratories do not do exhaustive DNA investigations for alpha-thalassemia. "
12/01/1980 - "Kindred studies demonstrate a correlation of the degree of anemia, microcytosis, and elevated hemoglobin A2 levels in affected family members (r = 0.318 P < 0.004, r = 0.525 P < 0.001, r = 0.416 P < 0.0015, respectively). "
08/01/2006 - "without microcytic anemia) increase of hemoglobin A2 (HbA2). "
06/01/1982 - "There was no statistically significant difference between the two groups with respect to the degree of anemia, severity of hemolysis, or hemoglobin A2 levels. "
07/01/2008 - "In this family, all seven heterozygotes with this mutation presented with moderate anemia, jaundice, splenomegaly and elevated hemoglobin A2 levels. "
01/01/2000 - "A 55-year-old man was admitted to our hospital because of leukocytosis and microcytic anemia with hypochromia, target cells, and increased levels of hemoglobin A2 and hemoglobin F. "
|5.||Hypochromic Anemia (Chlorosis)
01/01/2013 - "Hemoglobin A2 Higher than 3.5 percent was reported as 3.5%.The prevalence of beta-thassemia minor with high hemoglobin A2 and microcytic hypochromic anemia was 3.5% (P-value). "
01/01/2006 - "The prevalence of beta-thassemia trait with high hemoglobin A2 and microcytic hypochromic anemia was 3.4% (307/8918). "
03/01/1962 - "Hemoglobin A2 analysis in hypochromic anemias."
08/01/2014 - "The proband female presented with microcytic hypochromic anemia(hemoglobin 71 g/L, mean corpuscular volume 52.4 fl, mean corpuscular hemoglobin 16.1 pg), and hemoglobin A2 1.4%. "
01/01/1978 - "A 6-year-old child of northern European ancestry was found to have microcytic, hypochromic anemia with an elevated level of hemoglobin A2 and an unbalanced pattern of globin chain synthesis characteristic of beta-thalassemia trait. "
|2.||Fetal Hemoglobin (Hemoglobin F)
|6.||beta-Globins (beta Globin)