Hemoglobinopathies, including β-thalassemia and sickle cell disease (SCD), are common
genetic blood disorders. Endocrine disorders are frequent manifestations of organ damage …

Background The progression of osteoporosis (OP) can dramatically increase the risk of
fractures, which seriously disturb the life of elderly individuals. Specific protein 1 (SP1) is …

Objectives To determine the incidence of SP1 polymorphism in the COLIA1 gene and its
correlation to bone mineral density in patients with beta-thalassemia major (TM) …

Objective The objective of this study was to determine the frequency of transforming growth
factor beta 1 (TGFβ1) C-509T gene polymorphism and its relation to bone complications in …

Amaç: D vitamini, immün sistemdeki etkilerinin yanında kemik sağlığında önemli role
sahiptir. Çalışmamızda HIV-enfekte hastalarda D vitamini eksikliğinin sıklığını ve kemik …

Bone destruction by specialized multinuclear cells, osteoclasts, is important for physiological
processes of bone remodeling and tooth eruption. Osteoclasts are also critical contributors …

Objectives The objective of this article is to study the association of COLIA1 gene
polymorphism with osteoporosis in thalassemia major. Background Beta-thalassemia is a …

Objectives To determine the incidence of SP1 polymorphism in the COLIA1 gene and its
correlation to bone mineral density in patients with beta-thalassemia major (TM) …

Thalassemia Major is an inherited blood disorder which leads to ineffective erythropoiesis,
bone marrow expansion, and skeletal deformity. In the last two decades the survival of the …

Thalassemia Major is an inherited blood disorder which leads to ineffective erythropoiesis,
bone marrow expansion, and skeletal deformity. In the last two decades the survival of the …