Results 281 to 290 of about 1,975,307 (342)

THALASSEMIA-HEMOGLOBIN C DISEASE IN WHITE SIBLINGS

Pediatrics, 1956
Two white sisters of Italian parentage in whom thalassemia-hemoglobin C disease was found, have been presented. This is the third report of such cases and the first in white individuals. This disease produces a microcytic anemia which is usually mild but which may be severe. Splenomegaly may or may not be present.
M, ERLANDSON, C H, SMITH, I, SCHULMAN
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SICKLE CELL-HEMOGLOBIN C DISEASE

Annals of Internal Medicine, 1955
Excerpt Recent studies have shown that sickle hemoglobin can be differentiated electrophoretically from normal adult hemoglobin,1, 2and have also demonstrated the existence of a new abnormal hemogl...
E F, HAYS, R L, ENGLE
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Clinical presentation of sickle cell-hemoglobin C disease

The Journal of Pediatrics, 1986
Early symptoms were observed in a representative sample of 166 children with sickle cell-hemoglobin C disease diagnosed at birth. Symptoms were uncommon in the first year of life; in approximately 50% specific symptoms had developed by 5 years, but 22% remained without specific symptoms to 10 years.
S, Williams, G H, Maude, G R, Serjeant
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