|1.||Alkindi, Salam: 2 articles (11/2011 - 01/2010)|
|2.||Al Zadjali, Shoaib: 2 articles (11/2011 - 01/2010)|
|3.||Krishnamoorthy, Rajagopal: 2 articles (11/2011 - 01/2010)|
|4.||Daar, Shahina: 2 articles (11/2011 - 01/2010)|
|5.||Gravell, David: 2 articles (11/2011 - 01/2010)|
|6.||Balgir, R S: 2 articles (11/2008 - 12/2005)|
|7.||Souza, Renata Andréia Volpe: 1 article (10/2015)|
|8.||Souza, Bruna Maria Bereta de: 1 article (10/2015)|
|9.||Carlos, Aline Menezes: 1 article (10/2015)|
|10.||Martins, Paulo Roberto Juliano: 1 article (10/2015)|
|1.||beta-Thalassemia (Cooley's Anemia)
01/01/2012 - "In six patients, the Hb D traits were clinically symptomatic and behaved like those of thalassemia intermedia. "
01/01/2012 - "The heterozygous form of Hb D is clinically silent, but coinheritance of Hb D with Hb S or beta-thalassemia produces clinically significant conditions like thalassemia intermedia of moderate severity. "
04/01/2005 - "Hemoglobin D/beta-thalassemia and beta-thalassemia major in a Saudi family."
01/01/1979 - "Combinations of a Hb S heterozygosity with a heterozygosity for a Hb D-type of variant, for either one of two types of beta-thalassemia, two types of alpha beta- thalassemia, and five types of HPFH are discussed, and data are compared with those obtained for Hb S homozygotes. "
07/01/2000 - "With the rAAV constructs and hematopoietic stem cell (HSC) culture systems in hand, we are currently attempting to cure the mouse model of beta-thalassemia [C57BL/6- Hbbth/Hbbth, Hb(d-minor)] by HSC transplantation (HST) as well as by gene therapy. "
07/01/1961 - "Hemoglobinopathies in north India--1 hemoglobin D trait and hemoglobin D thelassemia."
04/01/2005 - "Although, compound heterozygous for Hb D/beta-thalassemia has been well described in the literature, our report emphasizes the importance of careful analysis of the electrophoresis results and the usefulness of molecular studies in premarital screening and other screening hemoglobinopathy programs."
10/01/2015 - "These findings corroborated of the National Neonatal Screening Program for diagnosing sickle cell disease and Hb C, Hb D, Hb E and β-thal hemoglobinopathies."
10/01/2008 - "Basic diagnosis of hemoglobinopathies can be performed by analysis of erythrocyte indices as well as by the separation and quantification of the common hemoglobin (Hb) fractions Hb A(2), Hb S, Hb C, Hb D, Hb E, and Hb F. "
10/01/1978 - "There were 72 cases of hemoglobinopathy: 65 thalassemia trait, four sickle-thalassemia, and one each of Hb D-thalassemia, sickle-C disease, and sickle-cell anemia. "
01/01/2011 - "Hematological studies of the family members showed that thalassemia which caused the mutations and Hb D were in the trans position."
07/01/2015 - "Serendipity: A Rare Discovery of Haemoglobin D-Iran in An Indian Female During Routine Antenatal Screening for β-Thalassemia."
07/01/2012 - "Hemoglobin D exist in four form; HbD trait, HbD-thalassemia, HbD sickle cell and HbD homozygous. "
11/01/2011 - "In a region such as Oman, where several genetic conditions of the red blood cell coexist (α- and β-thalassemia, Hb S, Hb D, Hb E) in significant frequencies, it is crucial to decipher the molecular basis of these atypical forms of β(+) thalassemias, especially in a genetic counseling setting."
01/01/2010 - "The overall carrier frequency of βTT was 4.05% and reinforces the differential frequency of β-thalassemia trait in schoolchildren from Delhi and Mumbai and the higher incidence of hemoglobin D in Punjabis as reported previously. "
|4.||Sickle Cell Anemia (Hemoglobin S Disease)
01/01/2009 - "To study the multi centric origin of this variant which is causing sickle cell disease in association with Hb S [beta6(A3)Glu-->Val, GAG>GTG], we have examined the haplotype of the Hb D allele in different populations. "
01/01/2013 - "Sickle cell hemoglobin D disease (HbSD) is a rare variant of sickle cell disease (SCD). "
07/01/2010 - "Sickle cell hemoglobin D disease is a rare variant of sickle cell disease. "
11/01/2008 - "Hemoglobin D after a red-cell exchange for sickle-cell disease."
08/01/2000 - "Homozygous Hb C and Hb S (sickle cell disease) produce significant clinical manifestations, whereas Hb E and Hb D homozygotes may be mildly symptomatic. "
|5.||Sickle Cell Trait
01/01/2003 - "Of 1064 couples aged 14-60 years recruited from the Public Health Laboratory, 49 had beta-thalassaemia trait, 69 had sickle-cell trait, 2 had haemoglobin D trait, 2 had haemoglobin C trait and 1 had high persistent fetal haemoglobin. "
08/01/1998 - "The incidence of haemoglobinopathies within the screened population was 2.62%, and comprised 0.69% beta thalassaemia trait, 1.22% sickle cell trait, 0.43% haemoglobin C trait and 0.26% haemoglobin D trait. "
01/01/1978 - "A case of sickle cell Hb D disease is reported in a young Iranian male, the father of whom carried an AS sickle cell trait and the mother an AD trait. "
01/01/2012 - "β-Thalassemia trait was found in 10.38%, Hb E [β26(B8)Glu→Lys] trait in 4.30%, sickle cell trait in 1.12%, borderline Hb A(2) value 0.73%, low Hb A(2) 0.68% and Hb D trait 0.37%. "
12/01/2005 - "Most common hemoglobinopathies observed out of 1015 cases were: sickle cell trait (29.8%), sickle cell disease (7.5%), sickle cell-beta-thalassemia (1.7%), beta-thalassemia trait (18.2%), thalassemia major (5.3%), thalassemia intermedia (0.9%), Hb E trait (0.9%), Hb E disease (0.3%), E-beta-thalassemia (0.7%), Hb D trait (0.2%) and SD disease (0.2%). "
|2.||Fetal Hemoglobin (Hemoglobin F)
|5.||hemoglobin D Punjab
|1.||Transplantation (Transplant Recipients)