Hereditary spherocytosis: Diagnostic and anaemia-associated aberrations of ghost proteins
Author:
Publisher
Informa UK Limited
Subject
Clinical Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/00365519409086515
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4. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
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1. Linkage of typically cytosolic peroxidases to erythrocyte membrane – A possible mechanism of protection in Hereditary Spherocytosis;Biochimica et Biophysica Acta (BBA) - Biomembranes;2020-03
2. Elevated levels of redox regulators, membrane-bound globin chains, and cytoskeletal protein fragments in hereditary spherocytosis erythrocyte proteome;European Journal of Haematology;2011-07-26
3. Aregenerative anemia and erythrocytes hemighosts: a case report;Annales de biologie clinique;2011-07
4. Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients;British Journal of Haematology;2010-03-21
5. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations;Blood Cells, Molecules, and Diseases;2007-05
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