366 related articles for article (PubMed ID: 11259161)
21. A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.
Jenkins PB; Abou-Alfa GK; Dhermy D; Bursaux E; Féo C; Scarpa AL; Lux SE; Garbarz M; Forget BG; Gallagher PG
J Clin Invest; 1996 Jan; 97(2):373-80. PubMed ID: 8567957
[TBL] [Abstract][Full Text] [Related]
22. Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy.
Li Y; Lu L; Li J
Cell Biochem Biophys; 2016 Sep; 74(3):365-71. PubMed ID: 27557951
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Flow cytometric measurement (H-1 Technicon) of microcytic and hyperchromic red cell populations in pediatric patients affected by hereditary spherocytosis (HS).
Ialongo P; Vignetti M; Cigliano G; Amadori S; Mandelli F
Haematologica; 1989; 74(6):547-53. PubMed ID: 2628236
[TBL] [Abstract][Full Text] [Related]
25. [Contribution of the spleen to the lipid metabolism in plasma and red cells. On hereditary spherocytosis and hereditary high red cell membrane phosphatidylcholine hemolytic anemia].
Sugihara T; Otsuka A; Yawata Y
Rinsho Ketsueki; 1989 Aug; 30(8):1248-55. PubMed ID: 2601042
[TBL] [Abstract][Full Text] [Related]
26. [Hereditary spherocytosis -- prevalence of erythrocyte membrane protein deficiency].
Granjo E; Manata P; Torres N; Rodrigues L; Ferreira F; Bauerle R; Quintanilha A
Acta Med Port; 2003; 16(2):65-9. PubMed ID: 12828006
[TBL] [Abstract][Full Text] [Related]
27. Abnormal membrane protein of red blood cells in hereditary spherocytosis.
Jacob HS; Ruby A; Overland ES; Mazia D
J Clin Invest; 1971 Sep; 50(9):1800-5. PubMed ID: 5564386
[TBL] [Abstract][Full Text] [Related]
28. Elevated levels of redox regulators, membrane-bound globin chains, and cytoskeletal protein fragments in hereditary spherocytosis erythrocyte proteome.
Saha S; Ramanathan R; Basu A; Banerjee D; Chakrabarti A
Eur J Haematol; 2011 Sep; 87(3):259-66. PubMed ID: 21575061
[TBL] [Abstract][Full Text] [Related]
29. [Erythrocyte indexes in hereditary spherocytosis].
Eberle SE; Sciuccati G; Bonduel M; Díaz L; Staciuk R; Torres AF
Medicina (B Aires); 2007; 67(6 Pt 2):698-700. PubMed ID: 18422060
[TBL] [Abstract][Full Text] [Related]
30. Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study.
Mullier F; Lainey E; Fenneteau O; Da Costa L; Schillinger F; Bailly N; Cornet Y; Chatelain C; Dogne JM; Chatelain B
Ann Hematol; 2011 Jul; 90(7):759-68. PubMed ID: 21181161
[TBL] [Abstract][Full Text] [Related]
31. Increased erythrocyte Ca2+ content in hereditary spherocytosis.
Feig SA; Bassilian S
Pediatr Res; 1975 Dec; 9(12):928-31. PubMed ID: 127974
[TBL] [Abstract][Full Text] [Related]
32. Abnormal phosphoenolpyruvate transport in erythrocytes of hereditary spherocytosis.
Ideguchi H; Hamasaki N; Ikehara Y
Acta Biol Med Ger; 1981; 40(4-5):555-8. PubMed ID: 7315102
[TBL] [Abstract][Full Text] [Related]
33. Erythrocyte energy metabolism in hereditary spherocytosis.
Reed CF; Young LE
J Clin Invest; 1967 Jul; 46(7):1196-204. PubMed ID: 6027083
[TBL] [Abstract][Full Text] [Related]
34. [Study of erythrocyte ion permeability in hereditary spherocytosis: contribution to its diagnosis].
Merino A; Vives Corrons L; Aguilar i Bascompte JL; Berga L; Reverter JC
Sangre (Barc); 1987; 32(3):323-32. PubMed ID: 2443989
[No Abstract] [Full Text] [Related]
35. Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis.
Crisp RL; Maltaneri RE; Vittori DC; Solari L; Gammella D; Schvartzman G; García E; Rapetti MC; Donato H; Nesse A
Ann Hematol; 2016 Oct; 95(10):1595-601. PubMed ID: 27465156
[TBL] [Abstract][Full Text] [Related]
36. Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning role.
Ingrosso D; D'Angelo S; Perrotta S; d'Urzo G; Iolascon A; Perna AF; Galletti P; Zappia V; Miraglia del Giudice E
Br J Haematol; 1996 Apr; 93(1):38-41. PubMed ID: 8611472
[TBL] [Abstract][Full Text] [Related]
37. Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).
Jarolim P; Rubin HL; Liu SC; Cho MR; Brabec V; Derick LH; Yi SJ; Saad ST; Alper S; Brugnara C
J Clin Invest; 1994 Jan; 93(1):121-30. PubMed ID: 8282779
[TBL] [Abstract][Full Text] [Related]
38. Induction of band 3 aggregation in erythrocytes results in anti-band 3 autoantibody binding to the carbohydrate epitopes of band 3.
Ando K; Kikugawa K; Beppu M
Arch Biochem Biophys; 1997 Mar; 339(1):250-7. PubMed ID: 9056256
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. [Measurement of phospholipids in erythrocytes, plasma and platelets in a patient with hereditary spherocytosis].
César JM; Fernández I; Navarro JL
Sangre (Barc); 1989 Aug; 34(4):300-2. PubMed ID: 2772783
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
