DYSFUNCTION OF THE RED BLOOD CELL MEMBRANE IN HEREDITARY SPHEROCYTOSIS
- 1 February 1968
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 14 (2), 99-104
- https://doi.org/10.1111/j.1365-2141.1968.tb01479.x
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Concomitant Alterations of Sodium Flux and Membrane Phospholipid Metabolism in Red Blood Cells: Studies in Hereditary Spherocytosis*Journal of Clinical Investigation, 1967
- Formation of membranes by repeating unitsArchives of Biochemistry and Biophysics, 1967
- Metabolic dependence of the critical hemolytic volume of human erythrocytes: relationship to osmotic fragility and autohemolysis in hereditary spherocytosis and normal red cells.Journal of Clinical Investigation, 1966
- Erythrocyte lipid loss in hereditary spherocytosis.Journal of Clinical Investigation, 1966
- Adenosine Triphosphate Metabolism in Hereditary Spherocytosis*Journal of Clinical Investigation, 1965
- Increased Cell Membrane Permeability in the Pathogenesis of Hereditary Spherocytosis *Journal of Clinical Investigation, 1964
- Biological TransportAnnual Review of Biochemistry, 1963
- EFFECTS OF SULFHYDRYL INHIBITION ON RED BLOOD CELLS. I. MECHANISM OF HEMOLYSIS*Journal of Clinical Investigation, 1962
- SODIUM TRANSPORT ACROSS THE SURFACE MEMBRANE OF RED BLOOD CELLS IN HEREDITARY SPHEROCYTOSIS 1Journal of Clinical Investigation, 1957
- The rate of sodium extrusion from human erythrocytesThe Journal of Physiology, 1953