Results 121 to 130 of about 607,752 (259)
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
Beta Thalassemia and Chronic Myeloid Leukemia: Dual Diagnosis Under the Microscope
International Journal of Laboratory Hematology, EarlyView.
Paige Muir +3 more
wiley +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
The Longitudinal Effect of APOL1 Risk Alleles on Sickle Cell Anemia‐Associated Kidney Function
American Journal of Hematology, Volume 101, Issue 6, Page 1341-1350, June 2026.ABSTRACT Progressive kidney injury is a major cause of morbidity and mortality in sickle cell anemia (SCA). The high risk APOL1 G1/G2 variants contribute to the development of kidney disease in individuals of African ancestry, including those with SCA.
Sara R. Rashkin +7 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.Graphical abstract summarizing a case of new‐onset HFrEF associated with profound microcytic anemia, highlighting severe anemia as a potential reversible trigger of acute cardiac decompensation. ABSTRACT Severe microcytic anemia may serve as a potentially reversible precipitating factor in heart failure with reduced ejection fraction (HFrEF). This case
Annabel Ricci +5 more
wiley +1 more source
HemaSphere, Volume 10, Issue 6, June 2026.Abstract Thalassemia and sickle cell disease (SCD) are among the most common monogenic disorders worldwide. They cause chronic hemolytic anemia, the consequences and prognosis of which vary considerably depending on the genetic characteristics of patients and the healthcare system in their country of residence.
Mariane de Montalembert +19 more
wiley +1 more source
Arthritis in beta‐thalassemia minor [PDF]
Arthritis & Rheumatism, 1983 L, Górriz +3 more
openaire +2 more sources
Síndromes talassêmicas diagnosticadas no Hospital Universitário - 1980 a 2004 [PDF]
, 2004 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Taneja, Atul Kumar
core
Compound Heterozygosity for Hemoglobin S and Hemoglobin LuLu Island
American Journal of Hematology, Volume 101, Issue 7, Page 1440-1442, July 2026.
Dana Lewis +4 more
wiley +1 more source