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6.345  Articles
1 of 635 pages  |  10  records  |  more records»
Objectives: To determine the frequency of endocrine disorders in Beta-Thalassemia Major (BTM) patients presenting for Endocrine Evaluation to the Department of Diabetes, Endocrinology and Metabolic Diseases, Hayatabad Medical Complex, Peshawar, Pakistan, ... see more

 
The clinical severity of beta-thalassemia disease ranges from mild to severe clinical manifestations, including beta-thalassemia major that requires more than six transfusions per year and is classified as transfusion dependant thalassemia (TDT). The pres... see more

Carrier screening for early detection of thalassemia in the general population needs a careful approach, especially in areas with limited health services. Various erythrocyte indices have been introduced as options for the first stage; however, ... see more

Objective: To observe the role of Mentzer index for differentiating iron deficiency anemia (IDA) and beta thalassemia trait (ß TT) in pregnant women.Methods: This cross-sectional study was conducted in Gynaecology & Obstetrics Department of Nishtar Me... see more

Beta-thalassemia major (BTM) is difficult to treat chronic disease, causing physical and psychological burdens for the patient. Several studies have confirmed a decrease in physical activity and depression in thalassemia patients, but limited studies exam... see more

Thalassemia is a chronic disease with long-term treatment that increases the potential for impact on physical, cognitive, and psychological conditions. About 80% of patients with major thalassemia have at least one psychiatric disorder, depression is one ... see more

Beta major thalassemia was characterized by severe hereditary hemolytic anemia and suffered from retardation in growth, and facial skeletal alteration also narrower arches. The purpose of this research was to obtain data on intermolar width in the 9-14 ye... see more

Thalassemia beta major is a hereditary hemolytic anemia disease with various grades of severity, which can be found with no or less globin chain qualitative synthesis. The patient often experiences hepatosplenomegaly, growth retardation and bone disorder ... see more

Beta major thalassemia is a genetically inherited blood disorder due to a genetic mutation on the polypeptide chains of hemoglobin which is manifested in the growth and development of the tooth. The objectives of the investigation were to obtain differenc... see more

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