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Journal Abstract Search

139 related items for PubMed ID: 17339199

  • 1. Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene.
    Zdebska E, Iolascon A, Spychalska J, Perrotta S, Lanzara C, Smolenska-Sym G, Koscielak J.
    Haematologica; 2007 Mar; 92(3):427-8. PubMed ID: 17339199
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  • 2. Heterozygosity of CDAN II (HEMPAS) gene may be detected by the analysis of erythrocyte membrane glycoconjugates from healthy carriers.
    Zdebska E, Mendek-Czajkowska E, Ploski R, Woêniewicz B, Koscielak J.
    Haematologica; 2002 Feb; 87(2):126-30. PubMed ID: 11836161
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  • 3. Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and III.
    Zdebska E, Gołaszewska E, Fabijańska-Mitek J, Schachter H, Shalev H, Tamary H, Sandström H, Wahlin A, Kościelak J.
    Br J Haematol; 2001 Sep; 114(4):907-13. PubMed ID: 11564084
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  • 4. [Diagnosis and genetics of congenital dyserythropoietic anemias (CDA)].
    Rössler J, Havers W.
    Klin Padiatr; 2000 Sep; 212(4):153-8. PubMed ID: 10994542
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  • 5. Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis.
    Fukuda MN.
    Baillieres Clin Haematol; 1993 Jun; 6(2):493-511. PubMed ID: 8043936
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  • 6. Short report: erythrocyte membranes from a patient with congenital dyserythropoietic anaemia type I (CDA-I) show identical, although less pronounced, glycoconjugate abnormalities to those from patients with CDA-II (HEMPAS).
    Zdebska E, Woźniewicz B, Adamowicz-Salach A, Kościelak J.
    Br J Haematol; 2000 Sep; 110(4):998-1001. PubMed ID: 11054095
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  • 8. Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search.
    Gasparini P, Miraglia del Giudice E, Delaunay J, Totaro A, Granatiero M, Melchionda S, Zelante L, Iolascon A.
    Am J Hum Genet; 1997 Nov; 61(5):1112-6. PubMed ID: 9345103
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  • 9. 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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  • 11. 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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  • 12. A case of congenital dyserythropoietic anemia type II associated with hemochromatosis.
    Tamura H, Matsumoto G, Itakura Y, Terai H, Ikebuchi K, Mitarai T, Isoda K.
    Intern Med; 1992 Mar; 31(3):380-4. PubMed ID: 1611191
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  • 13. [Morphological studies of erythrocytes in congenital dyserythropoietic anemia type II].
    Koehler M, Schmidt-Riese L, Brandeis WE.
    Acta Haematol Pol; 1990 Mar; 21(2):144-52. PubMed ID: 2131714
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  • 14. Glycophorin A in two patients with congenital dyserythropoietic anemia type I and type II is partly unglycosylated.
    Zdebska E, Adamczyk-Popławska M, Kościelak J.
    Acta Biochim Pol; 2000 Mar; 47(3):773-9. PubMed ID: 11310976
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  • 15. Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): where are we now?
    Denecke J, Marquardt T.
    Biochim Biophys Acta; 2009 Sep; 1792(9):915-20. PubMed ID: 19150496
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  • 17. Congenital dyserythropoietic anemia type II: serologic and morphologic family study.
    Ricci P, Baccarani M, Biagini G, Preda P, Tomasini I, Zucchelli P, Tura S.
    Nouv Rev Fr Hematol (1978); 1979 Sep; 21(2):197-207. PubMed ID: 514807
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  • 19. [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 Sep; 77(1052):631-8. PubMed ID: 3916299
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  • 20. Decreased band 3 anion transport activity and band 3 clusterization in congenital dyserythropoietic anemia type II.
    De Franceschi L, Turrini F, del Giudice EM, Perrotta S, Olivieri O, Corrocher R, Mannu F, Iolascon A.
    Exp Hematol; 1998 Aug; 26(9):869-73. PubMed ID: 9694508
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