Results 121 to 130 of about 26,664 (228)
General health of beta-thalassemia major patients in Gorgan, Iran [PDF]
Background and Objective: Thalassemias is the most common inherited disease in the world. This study was designed to assess general health of patients with beta-thalassemia major in Gorgan, northern Iran. Materials and Methods: This descriptive study was
Mirbehbahani NB +3 more
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American Journal of Hematology, Volume 101, Issue 9, Page 2430-2434, September 2026.
Ferras Alashkar +10 more
wiley +1 more source
Genetic analysis of beta-thalassemia major and beta-thalassemia intermedia in Brazil [PDF]
The development of methodologies to identify the molecular lesions responsible for different types of beta-thalassemia has made it possible to correlate these data with clinical and hematological severity.
Kerbauy, J +7 more
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Breathless: Beta Thalassemia Major
Vassiliki Katsi +3 more
openaire +3 more sources
Non-invasive prenatal diagnosis of beta-thalassemia disease using digital PCR
IntroductionTo evaluate the performance of digital polymerase chain reaction (dPCR) as a non-invasive prenatal test (NIPT) for assessing the risk of the fetus being affected by beta-thalassemia major and beta-thalassemia/Hb E disease.MethodsThis cross ...
Chalit Tangwerapornpong +7 more
doaj +1 more source
Serum lipid profiles in patients with beta-thalassemia major and intermedia in southern Iran [PDF]
BACKGROUND: Beta-thalassemia is considered to be the most frequent hereditary blood disorder worldwide. Lipid abnormalities have been detected in different types of beta-thalassemia.
Behrang Samadi +4 more
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Endocrine complications in patients with major β-thalassemia
Background: Endocrine complications in patients with major β –thalassemia related to iron overload that the most important cause of mortality and morbidity in this patients.This study evaluate prevalence of endocrine complications in major ...
Parastoo Rostami +2 more
doaj
Evaluation of Antioxidant Status in Beta Thalassemia Major Patients in Sabah [PDF]
: In beta thalassemia major severe haemolysis and repeated blood transfusions lead to excess iron deposition in various body tissues. This secondary iron overload is thought to be responsible for peroxidative tissue injury and subsequent oxidative stress.
M Z Hoque +3 more
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Introduction: Children with beta thalassemia are on regular blood transfusions, which could result in iron deposition in the liver causing decreased synthesis of Vitamin D-25OH.
Anil Kumar Shrestha +10 more
doaj +1 more source
Metabolic abnormalities in patients with beta thalassemia major [PDF]
Objective: To assess the metabolic abnormalities in patients with beta thalassemia major. Methodology: It was a cross-sectional study conducted at Department of Pathology in collaboration with Department of Orthopedic Surgery, Sharif Medical and Dental
Salma Haq, Farooq Azam Khan, Maria Aslam
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