Global ETD Search
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Showing 1 to 4 of 4 for “"HAEMOLYTIC DISEASE OF THE NEWBORN"”.
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Congenital haemolytic disease (haemolytic disease of the newborn): a study of 157 cases, with special reference to the morbid anatomy and morbid histology of the disease process and to the pathogenesis of kernicterus
Congenital haemolytic disease is a disease complex which may easily be separated into three more or less distinct clinical entities. These are:
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Enzyme-linked immunosorbent assay for red cell antibody quantitation.
The aim of the project was to develop a solid phase enzyme-linked immunosorbent assay (ELISA) for the quantitation of red cell antibodies of any specificity. Binding of negatively charged reagent red blood cells (RBC) was achieved in microplate precoated with poly-L lysine (PLL). The optimum …
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Electrolyte changes during exchange transfusion in the newborn
In infants suffering from haemolytic disease of the newborn death from cardiac failure consequent upon prolonged anoxia can occur within the first twenty-four hours of life. If the infants survive this period the anoxia is relieved as blood oxygenation mechanisms become more efficient. …