COVID-19 and β-thalassemia: in lieu of evidence and vague nexus
HM Al-Kuraishy, MH Mazhar Ashour, HM Saad… - Annals of …, 2024 - Springer
Abstract Coronavirus disease 19 (COVID-19) is an infectious disease caused by severe
acute respiratory coronavirus 2 (SARS-CoV-2) causing acute systemic disorders and multi …
acute respiratory coronavirus 2 (SARS-CoV-2) causing acute systemic disorders and multi …
Evaluation of regulatory T cells frequency and FoxP3/GDF-15 gene expression in β-thalassemia major patients with and without alloantibody; correlation with serum …
N Shokrgozar, N Amirian, R Ranjbaran… - Annals of …, 2020 - Springer
Abstract β-thalassemia major is one of the most common hematologic disorders in the world.
It causes severe anemia and patients require regular blood transfusions, which causes …
It causes severe anemia and patients require regular blood transfusions, which causes …
Alteration of trace elements and T-cell subsets in patients with β-thalassemia major: influence of high ferritin level
Alteration of trace elements and T-cell subsets in patients... : The Egyptian Journal of
Haematology Alteration of trace elements and T-cell subsets in patients with β-thalassemia …
Haematology Alteration of trace elements and T-cell subsets in patients with β-thalassemia …
Study of serum leptin in children with beta thalassemia: Correlation with iron overload
AbstractBackground: Beta thalassemia is a hereditary blood dis-order with defective beta
chain formation. ß-thalassemia is a major public health problem in Egypt. Patients with multi …
chain formation. ß-thalassemia is a major public health problem in Egypt. Patients with multi …
Evaluation of Immune System Alterations in Children with β-Thalassemia Major: Single-Center Egyptian Study
MR Beshir, MB Abd-Alaziz, WI Ismail… - Zagazig University …, 2024 - zumj.journals.ekb.eg
Background: Beta-thalassemia is an inherited haemoglobin disorder that is common in the
Middle East and Africa. Various studies have attributed the increased susceptibility to …
Middle East and Africa. Various studies have attributed the increased susceptibility to …
ESTIMATION OF SOME IMMUNOLOGICAL PARAMETERS IN SPLENECTOMIZED AND NON-SPLENECTOMIZED THALASSEMIC PATIENTS.
MAD Saleh, MA Saleh… - Biochemical & Cellular …, 2020 - search.ebscohost.com
Thalassemia is a genetic disorder of hemoglobin production, patient with thalassemia major
and some intermediate needed regular blood transfusion for correction of anemia to keep …
and some intermediate needed regular blood transfusion for correction of anemia to keep …