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Gender Disparities in Psychological Disturbances and Quality of Life Among Adolescent and Adult Patients with Thalassemia: A Review
Thalassemia is a chronic disease caused by impaired globin chain synthesis, leading to
ineffective erythropoiesis, hemolysis, and chronic anemia. The treatment of patients with …
ineffective erythropoiesis, hemolysis, and chronic anemia. The treatment of patients with …
The toxic influence of excess free iron on red blood cells in the biophysical experiment: an in vitro study
Iron is needed for life‐essential processes, but free iron overload causes dangerous clinical
consequences. The study of the role of red blood cells (RBCs) in the influence of excess free …
consequences. The study of the role of red blood cells (RBCs) in the influence of excess free …
Anemia and Its Determinants among Male and Female Adolescents in Southern Ethiopia: A Comparative Cross‐Sectional Study
Background. Adolescent anemia is a major public health problem worldwide. Adolescents
(10–19 years) are at an increased risk of develo** anemia due to increased iron demand …
(10–19 years) are at an increased risk of develo** anemia due to increased iron demand …
Determinant factors of children's blood lead levels in Java, Indonesia
Introduction Lead poisoning contributes to a significant burden of disease as a toxic
substance found in air, soil, and water. In Indonesia, the risk of exposure is high due to the …
substance found in air, soil, and water. In Indonesia, the risk of exposure is high due to the …
Diagnostic Modalities in Detecting Cardiovascular Complications of Thalassemia
Thalassemia major is the most common monogenetic disorder worldwide, manifested as
chronic hemolytic anemia. This condition leads to the need for chronic blood transfusion to …
chronic hemolytic anemia. This condition leads to the need for chronic blood transfusion to …
Correlation between plasma biochemical parameters and cardio-hepatic iron deposition in thalassemia major patients
Abstract Introduction Major Thalassemia patients suffer from iron overload and organ
damage, especially heart and liver damage. Early diagnosis and treatment with a chelator …
damage, especially heart and liver damage. Early diagnosis and treatment with a chelator …
[HTML][HTML] Iron overload and liver function in patients with beta thalassemia major: A cross sectional study
A Faruqi, T Zafar, S Subuctageen… - Pakistan Journal of …, 2024 - pmc.ncbi.nlm.nih.gov
Objective: In thalassemia major, repeated blood transfusions result in iron overload causing
organ damage. The objective of this study was assessment of liver enzymes in patients with …
organ damage. The objective of this study was assessment of liver enzymes in patients with …
Korelasi Feritin dengan Sitokin Proinflamasi pada Pasien Talasemia Beta Di Kota Samarinda Kalimantan Timur
Introduction: Ferritin is a routine parameter used in the evaluation of iron overload in
thalassemia patients. Excess iron causes the formation of ROS, resulting in an oxidative …
thalassemia patients. Excess iron causes the formation of ROS, resulting in an oxidative …
[PDF][PDF] Spectrum of HBB gene variants and major endocrine complications in thalassemia patients of Pakistan
Objective: To determine the molecular characterisation of beta-thalassemia major patients,
pattern of major endocrine complications and its association with haemoglobin subunit beta …
pattern of major endocrine complications and its association with haemoglobin subunit beta …
[PDF][PDF] Correlation of Serum Ferritin Level with Heart T2 MRI in Transfusion Dependent Thalassemia: a Systematic Review and Meta-Analysis
Background: Cardiac complications in patients with transfusion-dependent thalassemia
(TDT) are one of the ma-jor causes of mortality in these patients which annually impose …
(TDT) are one of the ma-jor causes of mortality in these patients which annually impose …