Noun:

थॅलेसेमिया,

thalassaemias's Usage Examples:

provide some genetic resistance to malaria including sickle cell disease, thalassaemias, glucose-6-phosphate dehydrogenase, and possibly others.

Homozygote α0 thalassaemias, where numerous γ4 but no α-globins occur at all (referred to as Hb.

Consequences included natural selection for sickle-cell disease, thalassaemias, glucose-6-phosphate dehydrogenase deficiency, Southeast Asian ovalocytosis.

Both these phenomena occur in thalassaemias, with blood transfusion therapy being the major cause of iron overload.

haemoglobin synthesis in reticulocytes (immature red blood cells) and thalassaemias (inherited blood disorders).

recognition of his pioneering work on the clinical and molecular basis of the thalassaemias, and fundamental contributions to the unravelling of their heterogeneity.

these phenomena occur in thalassaemias, with blood transfusion therapy being the major cause of iron overload in thalassaemia major and increased GI absorption.

was awarded the Royal Medal by the Royal Society for his work on the thalassaemias.

specifically the haemoglobinopathies of sickle cell disease and the thalassaemias and other genetic modifiers.

elucidating the many forms of molecular pathology that may underlie thalassaemias, and for his leadership in promoting the application of molecular genetics.

"Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias".

provide genetic resistance to malaria, including sickle cell disease, thalassaemias and glucose-6-phosphate dehydrogenase.