Results 181 to 190 of about 2,697,911 (252)

HFE Gene Mutations Among β-Thalassemia Intermediate and β-Thalassemia Minor Individuals in Gaza Strip, Palestine

open access: yes, 2009
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]

open access: yesPLoS One
Sangsiwarit P   +6 more
europepmc   +1 more source

Outcomes with luspatercept in patients with β-thalassemia: a systematic review and meta-analysis. [PDF]

open access: yesAnn Hematol
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]

open access: yesAnn Hematol
Kabbara F   +8 more
europepmc   +1 more source

Elevated Hemoglobin A<sub>2</sub>: A Molecular Revisited, and Implications to β-Thalassemia Screening. [PDF]

open access: yesJ Clin Lab Anal
Singha K   +8 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]

open access: yesMed Int (Lond)
Amin TA   +10 more
europepmc   +1 more source

Cognitive Performance in Transfusion-Dependent Adults with β-Thalassemia in Bulgaria: A Case-Control Study. [PDF]

open access: yesNeurol Int
Babacheva V   +4 more
europepmc   +1 more source

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