Significant haemoglobinopathies: guidelines for screening and diagnosis
British Journal of Haematology, 149, 35–49, doi:10.1111/j.1365-2141.2009.08054.x
British Journal of Haematology, 149, 35–49, doi:10.1111/j.1365-2141.2009.08054.x
Neurologic complications are a major cause of morbidity and mortality in sickle
cell disease (SCD). In children with sickle cell
Sickle cell disease (SCD) affects 12 000–15 000 individuals in the UK. Whilst homozygous SCD (sickle cell anaemia — HbSS)
הנחיות האיגוד הישראלי להמטולוגיה ואונקולוגיה ילדים 2014
Renal disease is one of the most frequent and severe complications experienced by patients with sickle cell disease; its prevalence is
KEY POINTS
KEY POINTS
Patients with b-thalassemia major (TM) and other refractory anemias requiring regular blood transfusions accumulate iron that damages the liver, endocrine system, and most
The purpose of this article is to set forth our approach to diagnosing and managing the
thalassemias, including b-thalassemia intermedia and
Acute chest syndrome describes new respiratory symptoms and findings, often severe and progressive, in a child with sickle cell disease and
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