...Zhara A. Al-Ali; Rana K. Fallatah; Esra A. Aljaffer; Eman R. Albukhari; Neriman Sadek Al-Ali; Ziyad T. Al-Ghannam; Reem Sayeb Al-Atrash; Ahmed Alsuliman; Chittibabu Vatte Disease severity of sickle cell anemia is highly variable, and it is commonly accepted that fetal hemoglobin (HbF) levels play...

... or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Fetal hemoglobin Hemoglobinopathies Hereditary persistence of fetal hemoglobin...

... -Thalassemia Fetal Hemoglobin Thalassemia intermedia Acta haemat. 61: 27-32 (1979) Hematological and Hemoglobin Synthesis Studies in a Family with Thalassemia Trait J. Pagnier, K. P. E. Amegnizin, D. Labié and M. Hayat Institut de Pathologie Moléculaire Inserm U-15, Laboratoire Associé au CNRS n° 85...

.... Hemoglobin Istanbul Fetal hemoglobin Splenectomy Short Communications Acta haemat. 61: 295-297 (1979) Differences between Individuals with Hemoglobins Istanbul and Saint-Étienne {a2fi2 92F8 H is Gin)1 Muzaffer Aksoy and Sakir Erdem Section of Hematology, Internal Clinic of Istanbul Medical School, £apa...

...David S. Chudwin; Donald L. Rucknagel; Aaron P. Scholnik; Thomas A. Waldmann; Robert McIntire Fetal hemoglobin (HbF) concentrations were measured by a radial immunodiffusion assay in 233 patients with various malignancies. In 96 of these, α-fetoprotein (AFP) was also measured by radioimmunoassay...

... evaluations and 317 fetal hemoglobin (Hb F) determinations are presented. The data show that the Hb F levels are the highest in patients with haplotypes 3/3 and the lowest in those with haplotypes 20/20. This is reflected in differences in total hemoglobin, PCV value, and RBC counts, which are the lowest...

...K.L. Bourantas; I. Georgiou; K. Seferiadis Six sickle cell/β-thalassemia patients (3 males and 3 females) were treated with 500 U/kg body weight human recombinant erythropoietin (h-rEPO) along with 300 mg/day iron sulfate in two phases, for a period of 90 days. Fetal hemoglobin (HbF) was assayed...

... of a single A nucleotide within the exon 1, at codon 18, of the β-globin gene) associated with a deletion of the δβ-globin gene region, in a patient exhibiting high persistence of fetal hemoglobin. The novel mutation causes a frameshift with the generation of a UGA stop codon. Analysis of the parent’s DNA...

... patients dying before adulthood [ 5 ]. The reasons for this clinical diversity are not clear. In several previous studies, the interaction of sickle cell anemia and α-thalassemia [ 6, 7 ], the level of fetal hemoglobin [ 8 ], as well as the β s -globin gene haplotypes were considered as potential...