Results 101 to 110 of about 36,735 (203)
Therapeutic Value of Silymarin as Iron Chelator in Children with Beta Thalassemia with Iron Overload
Mediterranean Journal of Hematology and Infectious Diseases, 2014 Beta thalassemia is an inherited hemoglobin disorder resulting in chronic hemolytic anemia. The most common treatment for thalassemia is blood transfusion which is necessary to provide the patients with healthy red blood cells containing normal ...
adel abd elhaleim hagag
doaj
Untreated Thalassemia Associated With Facial and Dental Changes in Adulthood
eJHaem, Volume 7, Issue 4, August 2026.
Miranda Lin, Ivana Ho, Richard C. Godby
wiley +1 more source
Khyber Medical University Journal, 2018 OBJECTIVE: To determine the frequency of beta thalassemia trait in pregnant anemic patients attending Khyber Teaching Hospital, Peshawar, Pakistan. METHODS: This descriptive cross sectional study was conducted in Gynecology and Obstetrics Department of ...
Maimoona Qadir, Sohail Amir
doaj
International Research Journal of Modernization in Engineering Technology and Science, 2023 openaire +1 more source
Prenatal Diagnosis of Compound Heterozygous Beta-Thalassemia: A Report of Two Cases. [PDF]
CureusJha S +4 more
europepmc +1 more source
How I manage luspatercept in transfusion-dependent beta-thalassemia. [PDF]
HemaspherePanzieri DL +5 more
europepmc +1 more source
Osteoporosis risk in alpha and beta thalassemia: An age- and sex-specific retrospective cohort study. [PDF]
Arch OsteoporosHsu YS, Tseng SC, Chao TF, Chen KH.
europepmc +1 more source
Behind the splenomegaly: a parasitic twist in siblings with beta thalassemia trait. [PDF]
BMC PediatrAli A +4 more
europepmc +1 more source
Evaluation of heart rate variability in pediatric patients with beta thalassemia major: Cross-sectional study. [PDF]
World J Clin PediatrSorour EA +5 more
europepmc +1 more source