Results 21 to 30 of about 920,848 (226)
Correlation between Serum Ferritin, Serum Cystatin C, and Renal Function in Children with β Thalassemia Major [PDF]
Majalah Kedokteran Bandung, 2019 Renal dysfunction caused by iron overload is characterized by an increase in ferritin and cystatin C levels. The objective of this study was to determine the correlation between ferritin, cystatin C, and renal function in children with β thalassemia major.
Suci Saptyuni Permadi +2 more
openaire +2 more sources
Alpha and beta-Thalassemia mutations in Hubei area of China
BMC Medical Genetics, 2020 Background Thalassemia is a group of inherited hemoglobic disorders resulting from defects in the synthesis of one or more of the hemoglobin chains, which is one of the most prevalent inherited disorders in southern China.
Yaowu Zhu +4 more
doaj +1 more source
Immunity to Pneumococcal Vaccine in Splenectomized β-Thalassemia Patients [PDF]
American Journal of Immunology, 2012 Problem statement: Splenectomy is accompanied by a lifelong risk of overwhelming post splenectomy infection, mainly caused by encapsulated bacteria such as Streptococcus pneumoniae. The mortality rate in those infected patients remains high. Therefore the pneumococcal polysaccharide vaccine has been recommended.
openaire +1 more source
Protein C and Protein S Levels in β-Thalassemia Major Patients in Erbil, Kurdistan Region
Cellular and Molecular Biology, 2020 Oxygen is transported in the blood through red blood cells and a protein called hemoglobin. The protein consists of two alpha and two beta chains. The lack of any of these chains is caused by the malfunction of the genes that produce them, and can lead to a genetic disease called thalassemia.
Tareefa Kakakhan, Hadi +2 more
openaire +3 more sources
, 2023 β-thalassemia mutations identified among 2,555 at-risk couples for β-thalassemia diseases including β0- thalassemia (2,479 alleles) and β+-thalassemia (224 alleles) and unknown (24 alleles).
Supawadee Yamsri (15295465) +6 more
core +1 more source
, 2023 Beta-thalassemia is a genetic blood disorder represented by anomalies in hemoglobin’s beta chain production. Most hemoglobin defects are a result of mutations of the structural β-globin gene.
Sima Alkilani (14586205) +1 more
core +1 more source
Alpha-Hemoglobin Stabilizing Protein Gene Polymorphism (rs4499252 A/G) and its Association with Beta-Thalassemia Major in Iraqi Patients [PDF]
Archives of Razi Institute, 2022 Beta thalassemia (β-thalassemia) major is a genetic disorder of hemoglobin production that results in a diminished rate of synthesis of one or more of the globin chains causing variable degrees of anemia.
M Adnan Khalaf +3 more
doaj +1 more source
A Comparison of Intelligence Quotient in Children with and without β-Thalassemia Major
Galen Medical Journal, 2015 Background: Thalassemia is the most common hemoglobinopathy worldwide. Children with β-thalassemia major have several risk factors for cognitive problems. The aim of this study is to evaluate intelligence quotient in children with β-thalassemia major and healthy counterparts using Wechsler Intelligence Scale.
Samaneh Homayouni Meymandi +2 more
openaire +2 more sources
β-THALASSEMIA TRAIT MENGGUNAKAN ELEKTROFORESIS MIKROKAPILER
INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY, 2018 Thalassemia is a genetic disorder disease which spread in the different parts of the world, including Indonesia. The incidence of β-thalassemia trait in Indonesia is between 3−8%. The objective of this study is to know the incidence of β-thalassemia trait in studentswho performed medical check-up, which obtain by using capilary electrophoresis, to ...
Nuryanti Nuryanti +2 more
openaire +2 more sources
Hematological Parameters in Individuals with Beta Thalassemia Trait in South Sumatra, Indonesia
Anemia, 2022 Background. β-Thalassemia has a very wide clinical variation, depending on the severity of the patient’s condition. Individuals with β-thalassemia traits are usually asymptomatic; however, laboratory examination will show mild anemia with microcytic ...
Dian Puspita Sari +5 more
doaj +1 more source