FREQUENCY OF BETA THALASSEMIA TRAIT AMONG THE HEALTHY INDIVIDUALS - A SINGLE CENTRE STUDY
Pakistan Armed Forces Medical Journal, 2018 Objective: To determine the frequency of beta thalassemia trait among the asymptomatic healthy individuals. Study Design: Cross sectional study. Place and Duration of Study: This was carried out at Pakistan Air Force (PAF) Hospital Lahore from ...
Muhammad Arif Sadiq +3 more
doaj
Is there an association of giardiasis with beta-thalassemia minor? [PDF]
, 2010 Beta–thalassemia minor is a symptomless carrier state of a hemoglobinopathy which predisposes to bacterial infections. We report three cases presenting with giardiasis, a parasitic infection of gastrointestinal tract caused by Giardia lamblia.
Jafri, Wasim +2 more
core +1 more source
Pre-Natal Diagnosis of beta – Thalassemia by Chorionic Villous Sampling
Journal of Rawalpindi Medical College, 2009 Background: To promote the utility of Chorionic Villous Sampling (CVS) for pre-natal diagnosis of beta thalassemia in at risk population and to highlight its demographic area distribution and effect of consanguinity.
Shazia Syed,
doaj
Comparison of the effects of lecture and booklet methods on awareness and attention of parents of children with Thalassemia major [PDF]
, 2008 چکیده: زمینه و هدف: تالاسمی از مهمترین بیماریهای ژنتیک است که مشکلات زیادی برای بیماران مبتلا ایجاد کرده است. با آموزش والدین می توان از بروز مشکلات جبران ناپذیر و عوارض خطرناک این بیماری پیشگیری و یا آنها را به حداقل رساند.
Delaram, Masoumeh. +8 more
core
Splenectomy in β‐thalassemia patients: Practices and risks in a nationwide study
HemaSphere, Volume 10, Issue 5, May 2026.
Audrey Benoit +194 more
wiley +1 more source
Frequency of T lymphocyte subsets in major beta-thalassemia patients and the influencing factors [PDF]
, 2013 زمینه و هدف: از راهکارهای رایج درمانی در بیماران تالاسمی تزریق خون های مکرر و درمان دفع آهن است. عوارض عفونی از مشکلات جدی در بیماران تالاسمی به حساب می آید که می تواند ناشی از ناهنجاری های ایمیونولوژیکی باشد.
Beshkar, Pezhman. +6 more
core
Microalbuminuria as Predictor of Early Glomerular Injury in Children and Adolescents with Sickle Cell Anaemia at Muhimbili National Hospital Dar es Salaam, Tanzania 2012 [PDF]
, 2012 Microalbuminuria (MA) is the earliest marker of various diseases affecting the renal system. Its relevance in children and adolescents with sickle cell anaemia (SCA), who are known to be prone to renal complications, has not been fully explored in our ...
Christopher, Richard
core
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