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23. [Molecular aspects of erythrocyte membrane disorders]. Saad ST; Costa FF Rev Assoc Med Bras (1992); 1994; 40(3):216-24. PubMed ID: 7787875 [No Abstract] [Full Text] [Related]
24. Grandeur in the red blood cell. Young LE Hosp Pract (Off Ed); 1984 Oct; 19(10):16-7, 20, 22. PubMed ID: 6434556 [No Abstract] [Full Text] [Related]
25. Disorders of red cell membrane skeleton: an overview. Palek J Prog Clin Biol Res; 1984; 159():177-89. PubMed ID: 6382324 [No Abstract] [Full Text] [Related]
26. [Cytoskeleton anomalies in disorders of red cell membrane proteins]. Kanzaki A; Wada H; Yawata Y Rinsho Ketsueki; 1991 Jun; 32(6):573-9. PubMed ID: 1832469 [TBL] [Abstract][Full Text] [Related]
27. Combination of hereditary elliptocytosis and hereditary spherocytosis. Aksoy M; Erdem S; Dincol G; Erdogan G; Cilingiroglu K; Dincol K Clin Genet; 1974; 6(1):46-50. PubMed ID: 4426130 [No Abstract] [Full Text] [Related]
28. Partial deficiency of protein 4.1 in hereditary elliptocytosis. Lambert S; Zail S Am J Hematol; 1987 Nov; 26(3):263-72. PubMed ID: 3674005 [TBL] [Abstract][Full Text] [Related]
29. Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis. Delaunay J; Alloisio N; Morle L; Baklouti F; Dalla Venezia N; Maillet P; Wilmotte R Ann Genet; 1996; 39(4):209-21. PubMed ID: 9037349 [TBL] [Abstract][Full Text] [Related]
30. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity]. Eber SW Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935 [TBL] [Abstract][Full Text] [Related]
31. Recent progress in studies on red cell membrane disorders. Yawata Y Nihon Ketsueki Gakkai Zasshi; 1988 Dec; 51(8):1360-71. PubMed ID: 3073612 [No Abstract] [Full Text] [Related]
32. Disorders of red cell membrane. An X; Mohandas N Br J Haematol; 2008 May; 141(3):367-75. PubMed ID: 18341630 [TBL] [Abstract][Full Text] [Related]
33. [Hereditary elliptocytosis with detection of a membrane protein defect of erythrocytes]. Hochhaus A; Wutke K; Meyer M Z Gesamte Inn Med; 1988 Mar; 43(5):128-9. PubMed ID: 3388917 [TBL] [Abstract][Full Text] [Related]
34. Hemolytic anemias due to disorders of red cell membrane skeleton. Bossi D; Russo M Mol Aspects Med; 1996 Apr; 17(2):171-88. PubMed ID: 8813717 [TBL] [Abstract][Full Text] [Related]
35. Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency. Conboy J; Mohandas N; Tchernia G; Kan YW N Engl J Med; 1986 Sep; 315(11):680-5. PubMed ID: 3755799 [TBL] [Abstract][Full Text] [Related]
36. 4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis. Perrotta S; Iolascon A; Polito R; d'Urzo G; Conte ML; Miraglia del Giudice E Haematologica; 1999 Jul; 84(7):660-2. PubMed ID: 10406914 [No Abstract] [Full Text] [Related]
37. Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis. Gallagher PG; Forget BG Blood Cells Mol Dis; 1997 Dec; 23(3):417-21. PubMed ID: 9446757 [No Abstract] [Full Text] [Related]
38. The structural organization of skeletal proteins influences lipid translocation across erythrocyte membrane. Mohandas N; Rossi M; Bernstein S; Ballas S; Ravindranath Y; Wyatt J; Mentzer W J Biol Chem; 1985 Nov; 260(26):14264-8. PubMed ID: 4055777 [TBL] [Abstract][Full Text] [Related]