|1.||Higgins, Trefor N: 3 articles (09/2015 - 03/2009)|
|2.||Rahimi, Zohreh: 3 articles (01/2011 - 04/2006)|
|3.||Mashon, Ranjeet S: 2 articles (01/2015 - 01/2010)|
|4.||Dass, Jasmita: 2 articles (09/2014 - 10/2013)|
|5.||Abdulrahman, Mahera: 2 articles (01/2013 - 01/2013)|
|6.||Belhoul, Khawla M: 2 articles (01/2013 - 01/2013)|
|7.||Saxena, R: 2 articles (07/2012 - 10/2007)|
|8.||Estey, Mathew P: 1 article (09/2015)|
|9.||Barakauskas, Vilte: 1 article (09/2015)|
|10.||Bordeleau, Pierre: 1 article (09/2015)|
03/15/1997 - "The present report described the hematologic and molecular study of the second case of Hb D-Punjab associated with a beta zero-thalassemia found in Spain and the first case in which the mutations have been identified at molecular level. "
01/01/2015 - "We present the diagnostic utility of high performance liquid chromatography (HPLC) in differential diagnosis between the Hb D-Punjab homozygote and the Hb D-Punjab/β-thalassemia (β-thal) genotype. "
01/01/2015 - "Coinheritance of Hb D-Punjab and β-thalassemia: diagnosis and implications in prenatal diagnosis."
01/01/2013 - "Compound heterozygosity for Hb D-Punjab [β121(GH4)Glu→Gln, GAA>CAA] /β-thalassemia (β-thal) must be carefully differentiated from homozygous Hb D-Punjab in premarital screening. "
07/01/2012 - "Here we present a case of HbD Punjab with α 3.7 kb deletion and IVS-1-5 β-thalassemia across a family. "
01/01/2010 - "In a study of sickle cell hemoglobinopathies, we detected the Hb D-Punjab mutation in 25 subjects from 11 unrelated Agharia families. "
09/01/2015 - "HPLC and electrophoresis suggested a complex α- and β-chain hemoglobinopathy with presumptive identification of the beta Hb variant as Hb D-Punjab. "
07/01/2015 - "Regarding hemoglobinopathies, 7% were classified as α-chain variants and 93% as β-chain variants with HbS (46%), HbE (16%), HbD Punjab (8%) and HbC (7%) traits being the most prevalent. "
02/01/2012 - "A novel double heterozygous, HbD Punjab/HbQ India, hemoglobinopathy."
01/01/1984 - "Hemoglobin SD-Los Angeles is an uncommon sickle hemoglobinopathy. "
|3.||beta-Thalassemia (Cooley's Anemia)
10/01/2007 - "The studies on the parents showed that mother was a compound heterozygote for HbD(Punjab) and HbC while father had beta-thalassemia trait. "
03/01/2015 - "Among them 12 (0.076 %) cases were double heterozygous for Hb-S and beta thalassemia minor (SB+), 2 (0.012 %) cases were double heterozygous for Hb-S and Hb-E (S/HBE), 1 (0.006 %) case was double heterozygous for Hb-S and Hb-D Punjab (S/HBD) and 22 (0.14 %) cases had Hb-S with Hb-F level more than 20 % (SSF). "
07/01/2013 - "Frequency of beta-Thalassemia trait was highest followed by beta-Thalassemia major, HbE trait, HbD Punjab and Hb intermedia. "
03/01/2009 - "HbA(2) was quantified on whole blood samples from patients with and without beta-thalassemia trait and patients heterozygous for HbE, HbS, HbC, and HbD Punjab using the VARIANT II beta-thalassemia (Bio-Rad, Hercules, CA) and Capillarys 2 (Sebia, Norcross, GA). "
04/01/2005 - "The other 2 children have Hb D Punjab traits while 2 other children have beta-thalassemia traits. "
|4.||Sickle Cell Anemia (Hemoglobin S Disease)
09/01/1990 - "Unusual sickle cell disease observed for the first time in Italy: Hb S-Hb D Los Angeles."
01/01/1985 - "[Disease caused by sickle cell anemia and hemoglobin D-Punjab. "
01/01/1984 - "We suggest that children with Hb SD-Los Angeles are at similar risks for the life-threatening complications which characterize sickle cell anemia and should receive the same comprehensive medical care currently recommended for children with Hb SS disease."
01/01/2010 - "We detected 28 subjects carrier for Hb D-Punjab (42.4%), 21 individuals carrier of Hb Q-Iran (31.8%), 12 subjects heterozygous for Hb Setif (18.2%), four cases with sickle cell disease (6.1%), and one case with Hb C (1.5%). "
01/01/2011 - "Hemoglobin S in homozygous state or in combination with one of the structural variants of Hb D-Punjab, Hb O-Arab, Hb C or β-thalassemia mutation results in sickle cell disease (SCD) that is characterized by chronic hemolytic anemia and tissue injury secondary to vasooclusion. "
|5.||Sickle Cell Trait
12/01/1994 - "Blood from subjects with sickle cell trait, Hb S/C disease, and various beta-thalassemias were analyzed by cIEF in < 15 min. cIEF was used to separate Hb S from Hb D-Los Angeles. "
01/01/2009 - "This hemoglobin genotype is associated with a benign clinical course, much like the sickle cell trait; however, its laboratory characteristics are very similar to compound heterozygous hemoglobin S and hemoglobin D-Los Angeles [beta121(GH4)Glu121Gln], which produces severe sickling hemolytic anemia. "
04/01/2013 - "There were 455 cases of β thalassemia trait, 24 β thalassemia major, 20 thalassemia inter-media, 54 sickle cell trait, fivesickle cell disease, 21 double heterozygous β thalassemia-sickle cell trait, nineand 4 Hb D- Punjab heterozygous and homozygous respectively, three Hb D β Thalassemia trait, 20 and 37 Hb E homozygous and heterozygous respectively, three Hb E β Thalassemia trait and four cases of Hb Q India. "
|1.||hemoglobin Q India
|8.||hemoglobin D Punjab
|9.||beta-Globins (beta Globin)