Background: Hereditary hemochromatosis (HH) is an autosomal recessive disorder of iron metabolism caused by mutations in the HFE gene. Objectives: The aim of this study was to determine the occurrence of C282Y and H63D mutations among β–thalassemia ...
Abed, Abdalla +2 more
core
Functional alterations of neutrophils from β-thalassemia patients exposed to Pythium insidiosum: An ex vivo study. [PDF]
Sangsiwarit P +6 more
europepmc +1 more source
Outcomes with luspatercept in patients with β-thalassemia: a systematic review and meta-analysis. [PDF]
Babiker N +9 more
europepmc +1 more source
Liver iron concentration and renal dysfunction in β-thalassemia: a case series and exploratory clinical observations. [PDF]
Kabbara F +8 more
europepmc +1 more source
Elevated Hemoglobin A<sub>2</sub>: A Molecular Revisited, and Implications to β-Thalassemia Screening. [PDF]
Singha K +8 more
europepmc +1 more source
Genotype distribution and identification of rare variants in α/β-thalassemia in chengdu: including the first report of HBA1:c.300+48C > G. [PDF]
Liu X +7 more
europepmc +1 more source
Crohn's disease and ulcerative colitis in β-thalassemia major: A report of two cases and a brief review of the literature. [PDF]
Amin TA +10 more
europepmc +1 more source
Cognitive Performance in Transfusion-Dependent Adults with β-Thalassemia in Bulgaria: A Case-Control Study. [PDF]
Babacheva V +4 more
europepmc +1 more source
Growth Profile and Endocrine Dysfunction in Children Aged 2-10 Years With Transfusion-Dependent β-Thalassemia Major. [PDF]
Tripathi A +5 more
europepmc +1 more source
Determinants of retinal and choriocapillaris microvascular alterations in pediatric β-thalassemia: an OCTA study. [PDF]
Amin MR, Youssef MM, Ali AA, Hassan LM.
europepmc +1 more source

