Correlation of oxidative stress with serum trace element levels and antioxidant enzyme status in Beta thalassemia major patients: a review of the literature
Beta thalassemia major is an inherited disease resulting from reduction or total lack of beta
globin chains. Patients with this disease need repeated blood transfusion for survival. This …
globin chains. Patients with this disease need repeated blood transfusion for survival. This …
Review of endocrine complications in transfusion-dependent thalassemia
Beta thalassemia is an inherited genetic disorder that often leads to transfusion
dependence. One of the significant issues that these patients face is increased iron …
dependence. One of the significant issues that these patients face is increased iron …
Sodium, magnesium, calcium, manganese, iron, copper, and zinc in serums of beta thalassemia major patients
Thalassemia major is the most severe form of thalassemia and occurs with the impaired
synthesis of β-globin which causes the accumulation of unpaired alpha globin chain …
synthesis of β-globin which causes the accumulation of unpaired alpha globin chain …
Increased zinc and albumin but lowered copper in children with transfusion-dependent thalassemia
Background Measurements of copper and zinc in transfusion-dependent thalassemia (TDT)
show contradictory results. Aim of the study To examine serum levels of these minerals in …
show contradictory results. Aim of the study To examine serum levels of these minerals in …
Using LIBS as a diagnostic tool in pediatrics beta-thalassemia
J Alsharnoubi, Y Nassef, RF Fahmy, M Gamal - Lasers in Medical Science, 2021 - Springer
Beta-thalassemia major is a common inherited single-gene disorder. Thalassemic patients
are at risk of changes in some important trace elements. To detect alteration of iron, copper …
are at risk of changes in some important trace elements. To detect alteration of iron, copper …
[PDF][PDF] Hubungan Kepatuhan Konsumsi Kelasi Besi Terhadap Pertumbuhan Anak Dengan Thalassemia
M Syobri, FL Mustofa, N Triswanti - Jurnal Ilmiah Kesehatan Sandi …, 2020 - academia.edu
Abstrak Penyakit Thalassemia di Indonesia termasuk dalam kelompok negara yang berisiko
tinggi. Salah satu penyakit genetik yang tersering di dunia adalah penyakit thalasemia …
tinggi. Salah satu penyakit genetik yang tersering di dunia adalah penyakit thalasemia …
Effect of zinc supplementation on serum antibody titers to heat shock protein 27 in patients with thalassemia major
E Ghahramanlu, A Banihashem, NZ Mirhossini… - …, 2014 - Taylor & Francis
Objective This current study was conducted to determine the effect of zinc supplementation
on antibody titers to heat shock protein 27 (anti-HSP27) in patients with beta-thalassemia …
on antibody titers to heat shock protein 27 (anti-HSP27) in patients with beta-thalassemia …
Relationship between serum ferritin and zinc levels in patients with major thalassemia
Background In thalassemia patients, reduced zinc absorption results from increased serum
iron due to repeated blood transfusions, increased iron absorption due to ineffective …
iron due to repeated blood transfusions, increased iron absorption due to ineffective …
[PDF][PDF] Serum Trace Elements (Zinc, Copper and Magnesium) in Iraqi Patients with Thalassemia Major Receiving Desferrioxamine and its Relation with Growth State.
Z Naji - Iraqi Journal of Medical Sciences, 2012 - iasj.net
Background Patients with β-thalassemia major (TM) require periodic blood transfusion and
iron-chelating therapy for all their life and they frequently show complications like trace …
iron-chelating therapy for all their life and they frequently show complications like trace …
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 …