Results 111 to 120 of about 5,832,501 (223)

Association between Alpha- Klotho Protein, Calcium, and Phosphate concentrations in Adult Iraqi Patients with Beta-Thalassemia Major

مجلة كلية الطب
Background: Beta-thalassemia major is a prevalent global condition characterized by a rapid breakdown of red blood cells. Regular blood transfusions can give rise to problems such as cardiovascular disease, diabetes, osteoporosis, and renal disorders ...
Ahmed J. Kadhim, Hedef D. El-Yaseen, Ali M. Jawad   +2 more
doaj   +1 more source

Frequency and Levels of Autoantibodies Among Women of Reproductive Age with Beta-Thalassemia Major: A Case-Control Study [PDF]

Journal of Mazandaran University of Medical Sciences
Background and purpose: Beta-thalassemia is an inherited haematological disorder, and patients may experience alterations and dysregulation of immune responses as a result of regular blood transfusions and iron overload.
Mehrshad Shams, Tamana Eskandari, Muhammad Malekian, Nilofar Dehghan, Hossein Jalali, Hossein Karami, Mohammad Naderisoraki, Hadi DarvishKhezri, Hossein Asgarian-Omran, Mohsen Tehrani, Saeid Taghiloo   +10 more
doaj  

Beta Thalassemia Major

, 2002
Beta Thalassemia ...
Lawrence, Christine
core  

Beta-thalassemia intermedia: an overview

, 2008
Thalassemias are inherited anemias characterized by decreased or absent globin chain synthesis and by ineffective erythropoesis. They are classified according to the defective globin chain and to the clinical severity.
A. Inati, A. Taher, M.D. Cappellini, F. El Rassi   +3 more
core   +2 more sources

An Investigation of Group-Based Mobile Learning on Stress, Anxiety, Depression, and Pain Among Beta-Thalassemia Major Patients: A Randomized Control Trial

Objective: Beta-thalassemia major (B-TM) is an inherited hematological disease that affects nearly 300 million people worldwide. This study aimed to evaluate the effects of group-based mobile learning on stress, anxiety, depression, and pain among beta ...
Mahsa Imanian, Ali Dehghani, Leili Mosalanejad   +2 more
core   +1 more source

Deferoxamine in thalassemia major.

, 1995
Comment on: Survival in medically treated patients with homozygous beta-thalassemia. [N Engl J Med. 1994] Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major.
CAZZOLA, MARIO, LOCATELLI, FRANCO, De Stefano P.   +2 more
core  

Breathless: Beta Thalassemia Major

The American Journal of Medicine, 2017
Vassiliki Katsi, Georgios Georgiopoulos, Georgia Vogiatzi, Dimitrios Tousoulis   +3 more
openaire   +3 more sources

The Evaluation of serum fucose and fucose related parameters in beta- thalassemia major

Zanco Journal of Medical Sciences
Background and objective: Beta-thalassemia syndrome is characterized by either absent or lower-than-normal production of the beta-globin chain in hemoglobin, which can cause various health problems.
Heba Hasan Jalal, Bakhtiar Muhialdin Ahmad   +1 more
doaj   +1 more source

Curcumin Therapy Reduces Iron Overload and Oxidative Stress in Beta-Thalassemia: Findings from a Meta-Analytic Study

The risk of anemia and iron overload is a global concern in beta (β)-thalassemia. The β-thalassemia primary treatment includes blood transfusion and iron chelation therapy; however, both are associated with risks such as anemia, iron depletion,
Perpetua Modjadji, Kabelo Mokgalaboni, Wendy N. Phoswa, Sogolo L. Lebelo   +3 more
core   +1 more source

Endocrine complications in patients with major β-thalassemia

Iranian South Medical Journal, 2011
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, Gisoo Hatami, Afshin Shirkani   +2 more
doaj