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Journal Abstract Search

134 related items for PubMed ID: 7055536

  • 1.
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  • 2. Incomplete glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (CDA II).
    Mawby WJ, Tanner MJ, Anstee DJ, Clamp JR.
    Br J Haematol; 1983 Oct; 55(2):357-68. PubMed ID: 6615729
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  • 3. Proteolytic dissection of band 3 protein from human erythrocyte in congenital dyserythropoietic anemia type II.
    Sansone G, Scartezzini P, Baldi M, Forni GL, Veneziano G.
    Pathologica; 1981 Oct; 73(1026):623-8. PubMed ID: 7312435
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  • 4. Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMP AS).
    Baines AJ, Banga JP, Gratzer WB, Linch DC, Huehns ER.
    Br J Haematol; 1982 Apr; 50(4):563-74. PubMed ID: 7066206
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  • 6. Glycolipids and glycopeptides of red cell membranes in congenital dyserythropoietic anaemia type II (CDA II).
    Zdebska E, Anselstetter V, Pacuszka T, Krauze R, Chełstowska A, Heimpel H, Kościelak J.
    Br J Haematol; 1987 Jul; 66(3):385-91. PubMed ID: 3620357
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  • 7. Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia.
    Pothier B, Morlé L, Alloisio N, Ducluzeau MT, Féo C, Blanchard D, Cartron JP, Garbarz M, Chaveroche I, Boivin P.
    Br J Haematol; 1987 Jul; 66(3):393-400. PubMed ID: 3620358
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  • 8. Alterations of globin chain synthesis and of red cell membrane proteins in congenital dyserythropoietic anemia I and II.
    Alloisio N, Jaccoud P, Dorleac E, Morle L, Philippe N, Margueritte G, Bryon PA, Delaunay J.
    Pediatr Res; 1982 Dec; 16(12):1016-21. PubMed ID: 6185913
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  • 9. Congenital dyserythropoietic anaemia (CDA) with severe gout, rare Kell phenotype and erythrocyte, granulocyte and platelet membrane reduplication: a new variant of CDA type II.
    Lowenthal RM, Marsden KA, Dewar CL, Thompson GR.
    Br J Haematol; 1980 Feb; 44(2):211-20. PubMed ID: 7378299
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  • 12. Decreased glycosylation of band 3 and band 4.5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II.
    Scartezzini P, Forni GL, Baldi M, Izzo C, Sansone G.
    Br J Haematol; 1982 Aug; 51(4):569-76. PubMed ID: 7104237
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  • 13. Congenital dyserythropoietic anaemia type II (HEMPAS): a family study.
    McCann SR, Firth R, Murray N, Temperley IJ.
    J Clin Pathol; 1980 Dec; 33(12):1197-201. PubMed ID: 7451666
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  • 14. [Changes in erythrocyte membrane protein in congenital dyserythropoietic anemia type II (C.D.A.II, HEMPAS)].
    Scartezzini P, Forni GL, Baldi M, Veneziano G, Baffico M.
    Pathologica; 1985 Dec; 77(1052):631-8. PubMed ID: 3916299
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  • 17. Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS).
    Denecke J, Kranz C, Nimtz M, Conradt HS, Brune T, Heimpel H, Marquardt T.
    Glycoconj J; 2008 May; 25(4):375-82. PubMed ID: 18166993
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  • 18. Abnormal fatty acid composition of erythrocyte glycosphingolipids in congenital dyserythropoietic anemia type II.
    Bouhours JF, Bouhours D, Delaunay J.
    J Lipid Res; 1985 Apr; 26(4):435-41. PubMed ID: 4009062
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  • 19. Defective glycosylation of erythrocyte membrane glycoconjugates in a variant of congenital dyserythropoietic anemia type II: association of low level of membrane-bound form of galactosyltransferase.
    Fukuda MN, Masri KA, Dell A, Thonar EJ, Klier G, Lowenthal RM.
    Blood; 1989 Apr; 73(5):1331-9. PubMed ID: 2495036
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  • 20. Studies of ineffective erythropoiesis and peripheral haemolysis in congenital dyserythropoietic anaemia type II.
    Barosi G, Cazzola M, Stefanelli M, Ascari E.
    Br J Haematol; 1979 Oct; 43(2):243-50. PubMed ID: 508633
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