Variable clinical severity of hereditary spherocytosis: Relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis
- 1 September 1990
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 117 (3) , 409-416
- https://doi.org/10.1016/s0022-3476(05)81081-9
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding.Journal of Clinical Investigation, 1987
- Inheritance Pattern and Clinical Response to Splenectomy as a Reflection of Erythrocyte Spectrin Deficiency in Hereditary SpherocytosisNew England Journal of Medicine, 1986
- Hereditary SpherocytosisAnnals of Surgery, 1986
- Partial deficiency of erythrocyte spectrin in hereditary spherocytosisNature, 1985
- A Genetic Defect in the Binding of Protein 4.1 to Spectrin in a Kindred with Hereditary SpherocytosisNew England Journal of Medicine, 1982
- Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosisBlood, 1982
- Deficient Red-Cell Spectrin in Severe, Recessively Inherited SpherocytosisNew England Journal of Medicine, 1982
- Splenectomy in Hematologic DisordersNew England Journal of Medicine, 1972
- Red cell survival studies in hereditary spherocytosisJournal of Clinical Investigation, 1970
- Hereditary spherocytosisThe American Journal of Medicine, 1955