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Gallagher PG, Glader B. Hereditary spherocytosis, hereditary elliptocytosis, and other disorders associated with abnormalities of the erythrocyte membrane.
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Imaging of the diffusion of single band 3 molecules on normal and mutant erythrocytes. Integral protein linkage and the bilayerskeletal separation energy in red blood cells. Biophys J. Structures of the spectrin-ankyrin interaction binding domains. The structure of the ankyrin-binding site of beta-spectrin reveals how tandem spectrin-repeats generate unique ligand-binding properties. Protein 4. Blood Cell Molecules Dis. Biochem J. Ipsaro JJ, Mondrag A. Red Cells, Iron and erythropoiesis structural basis for spectrin recognition by ankyrin.
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Hydrogen ion dynamics in human red blood cells. J Physiol. Temperature -and hydrationdependent internal dynamics of stripped human erythrocyte vesicles studied by incoherent neutron scattering. Biochim Biophys Acta. Erythrocyte membrane protein analysis by sodium dodecyl sulphate-capillary gel electrophoresis in the diagnosis of hereditary spherocytosis.
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Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population. Int J Hematol. Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4. Partial splenectomy for hereditary spherocytosis. Pediatr Clin N Am. High frequency of de novo mutations in ankyrin gene ANK1 in children with hereditary spherocytosis. J Pediatr. Frequent de novo monoallelic expression of beta-spectrin gene SPTB in children with hereditary spherocytosis and isolated spectrin deficiency.
Erythrocyte membrane protein destabilization versus clinical outcome in Portuguese Hereditary Spherocytosis patients. Variable clinical severity of hereditary spherocytosis: Relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis. Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation.
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Esferocitosis hereditaria: de la biogénesis a la patogénesis.
Skip to search form Skip to main content You are currently offline. Some features of the site may not work correctly. La esferocitosis hereditaria es la anemia hemolitica congenita mas frecuente en la poblacion caucasica. Tiene una amplia variabilidad clinica y desde el punto de vista hematologico se caracteriza por anemia y presencia de esferocitos en la lamina periferica. Su base fisiopatologica esta determinada por el defecto de algunas de las proteinas que conforman la membrana eritrocitaria, por el efecto del bazo sobre los hematies anomalos y otros factores. View PDF.
2012, Número 4
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