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6. [Studies on the protein composition of red-cell membrane in hereditary spherocytosis (author's transl)]. Mazo E; Fernández J; Zubizarreta A; Rocha E Sangre (Barc); 1979; 24(4):376-88. PubMed ID: 483115 [No Abstract] [Full Text] [Related]
7. [Alteration of erythrocyte membrane proteins in a family with hereditary spherocytosis]. Inoue F; Matsuyama R; Yoneyama S Nihon Ketsueki Gakkai Zasshi; 1989 Nov; 52(7):1122-7. PubMed ID: 2618557 [TBL] [Abstract][Full Text] [Related]
8. Recent advances in the understanding of the erythrocyte membrane. Lam SK; Quah TC J Singapore Paediatr Soc; 1991; 33(3-4):140-8. PubMed ID: 1812330 [TBL] [Abstract][Full Text] [Related]
9. Higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 in hereditary spherocytosis (HS). Ayala S; Besson I; Aymerich M; Berga L; Vives Corrons JL Int J Hematol; 1995 Jul; 62(1):53-4. PubMed ID: 7670008 [No Abstract] [Full Text] [Related]
10. [Rheological properties of erythroblasts and erythrocytes in congenital spherocytosis]. Leblond PF; Lacelle PL; Weed RI Nouv Rev Fr Hematol; 1971; 11(4):537-46. PubMed ID: 4257429 [No Abstract] [Full Text] [Related]
14. Update on the clinical spectrum and genetics of red blood cell membrane disorders. Gallagher PG Curr Hematol Rep; 2004 Mar; 3(2):85-91. PubMed ID: 14965483 [TBL] [Abstract][Full Text] [Related]
15. Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis. King MJ; Telfer P; MacKinnon H; Langabeer L; McMahon C; Darbyshire P; Dhermy D Cytometry B Clin Cytom; 2008 Jul; 74(4):244-50. PubMed ID: 18454487 [TBL] [Abstract][Full Text] [Related]
16. The erythrocyte membrane abnormality of hereditary spherocytosis. Zail SS Br J Haematol; 1977 Nov; 37(3):305-10. PubMed ID: 146514 [No Abstract] [Full Text] [Related]
17. A new dimension in red cell morphology: a study of spherocytosis. Neser ML S Afr Med J; 1968 Dec; 42(47):Suppl:2-12. PubMed ID: 5719978 [No Abstract] [Full Text] [Related]
19. The red cell membrane in hemolytic anemia. Cooper RA; Shattil SJ Mod Treat; 1971 May; 8(2):329-51. PubMed ID: 4940517 [No Abstract] [Full Text] [Related]
20. Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis. Marík T; Kselíková M; Bíbr B; Brabec V; Lener J Folia Haematol Int Mag Klin Morphol Blutforsch; 1983; 110(1):81-5. PubMed ID: 6192057 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]