Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population

References

• Kar R, Rao S, Srinivas UM, Mishra P, Pati HP. Clinico-hematological profile of hereditary spherocytosis: experience from a tertiary care center in North India. Hematology. 2009;14(3):164–7.
   PubMed Web of Science ®Google Scholar
• Perrotta S, Gallagher PG, Mohandas N. Hereditary spherocytosis. Lancet. 2008;372(9647):1411–26.
   PubMed Web of Science ®Google Scholar
• Gallagher PG, Forget BG. Hereditary Spherocytosis, elliptocytosis and related disorders. In: , Beutler E, editor. Williams hematology. 6th ed. New York: McGraw-Hill; 2001. p. 503–18.
   Google Scholar
• Becker PS, Lux SE. Disorders of the red cell membrane. In: , Nathan D, Oski F, editors. Hematology of infancy and childhood. Philadephia, PA: WB Saunders; 1993. p. 529–605.
   Google Scholar
• Lux SE, Becker PS. Disorders of the red cell membrane skeleton, hereditary spherocytosis and hereditary elliptocytosis. In: The metabolic basis of inherited disease. 6th ed. New York: McGraw-Hill; 1989. p. 170–7.
   Google Scholar
• Tse WT, Lux SE. Hereditary spherocytosis and hereditary elliptocytosis. In: , Scriver C R, Beaudet A L, Sly W S, Valle D, editors. The metabolic and molecular bases of inherited disease. Vol. III. New York: McGraw-Hill; 2001. p. 4665–711.
   Google Scholar
• del Giudice MiragliaE, Iolascon A, Pinto L, Nobili B, Perrotta S. Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis. Br J Haematol. 1994;88:52–5.
   PubMed Web of Science ®Google Scholar
• Delaunay J. Genetic disorders of the red cell membrane. Crit Rev Oncol Hematol. 1995;19:79–110.
   PubMed Web of Science ®Google Scholar
• Rocha S, Costa E, Rocha-Pereira P, Ferrira F, Cleto E, Barbot J, et al.. Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients. Br J Haematol. 2010;149(5):785–94.
   PubMed Web of Science ®Google Scholar
• Dodge JT, Mitchell C, Hanahan DJ. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes. Arc Biochem Biophys. 1963;100:119–30.
   PubMed Web of Science ®Google Scholar
• Fairbanks G, Steck TL, Wallach DF. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971;10:2606–17.
   PubMed Web of Science ®Google Scholar
• Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227:680–5.
   PubMed Web of Science ®Google Scholar
• Agre P, Casella JF, Zinkham WH, McMillan C, Bennett V. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis. Nature. 1985;314:380–3.
   PubMed Web of Science ®Google Scholar
• King MJ, Bhrens J, Rogers C, Flynn C, Greenwood D, Chambers K. Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anemia. Br J Haematol. 2000;111(3):942–3.
   Web of Science ®Google Scholar
• Young KL, Han IC, Sung SP. Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis. J Korean Med Sci. 2000;15:284–8.
   PubMed Web of Science ®Google Scholar
• Saad ST, Costa FF, Vicentim DL, Salles TS, Pranke PH. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil. Br J Haematol. 1994;88:295–9.
   PubMed Web of Science ®Google Scholar
• del Giudice MiragliaE, Iolascon A, Pinto L, Nobili B, Perrotta S. Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis. Br J Haematol. 1994;88:52–5.
   PubMed Web of Science ®Google Scholar
• Jarolim P, Murray JL, Rubin HL, Taylor WM, Prchal JT, Ballas SK. Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency. Blood. 1996;88:4366–74.
   PubMed Web of Science ®Google Scholar
• Tshilolo L, Kagambega F, Sztern B, Vertongen F, Gulbis B. Hereditary spherocytosis: one year study of erythrocyte membrane proteins. Rev Med Brux. 1998;19(5 Pt 1):417–23.
   PubMedGoogle Scholar
• Ricard MP, Gilsanz F, Millan I. Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases. Haematologica. 2000;85:994–5.
   PubMed Web of Science ®Google Scholar
• Savvides P, Shalev O, John KM, Lux SE. Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis. Blood. 1993;82:2953–60.
   PubMed Web of Science ®Google Scholar
• Agre P, Asimos A, Casella JF, McMillan C. Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis. N Eng J Med. 1986;315:1579.
   PubMed Web of Science ®Google Scholar
• Premetis E, Stamoulakatou A, Loukopoulos D. Erythropoiesis: hereditary spherocytosis in Greece: collective data on a large number of patients. Hematology. 1999;4:361–6.
   PubMedGoogle Scholar
• Mariani M, Bacellini W, Vercellati C, Marcello P, Fermo E, Pedotti P, et al.. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect. Haematologica. 2008;93(9):1310–7.
   PubMed Web of Science ®Google Scholar
• Cynober T, Mohandas N, Tchernia G. Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity. J Lab Clin Med. 1996;12:259–69.
   Google Scholar
• Rocha S, Rebelo I, Costa E, Catarino C, Belo L, Castro EB. Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis. Eur J Haematol. 2005;74:374–80.
   PubMed Web of Science ®Google Scholar
• Sanchez-Lopez JY, Camacho AL, Magana MT, Ibarra B, Perea FJ. Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis. Blood Cells Mol Dis. 2003;31:357–9.
   PubMed Web of Science ®Google Scholar
• Yawata Y, Kanzak A, Yawata A. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population. Int J Hematol. 2000;71:118–35.
   PubMed Web of Science ®Google Scholar