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Journal Abstract Search

255 related items for PubMed ID: 9009444

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  • 3. 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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  • 4. Congenital dyserythropoietic anemias: epidemiology, clinical significance, and progress in understanding their pathogenesis.
    Heimpel H.
    Ann Hematol; 2004 Oct; 83(10):613-21. PubMed ID: 15278299
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  • 5. 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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  • 6. [Localized gene of the rare "Norrland disease". CDA-III blood disease with dominant heredity].
    Sandström H, Wahlin A.
    Lakartidningen; 1999 Jan 27; 96(4):343-7. PubMed ID: 10024825
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  • 7. Congenital dyserythropoietic anemias.
    Marks PW, Mitus AJ.
    Am J Hematol; 1996 Jan 27; 51(1):55-63. PubMed ID: 8571938
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  • 10. Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapy.
    Goede JS, Benz R, Fehr J, Schwarz K, Heimpel H.
    Ann Hematol; 2006 Sep 27; 85(9):591-5. PubMed ID: 16767397
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  • 11. Advances in the understanding of the congenital dyserythropoietic anaemias.
    Wickramasinghe SN, Wood WG.
    Br J Haematol; 2005 Nov 27; 131(4):431-46. PubMed ID: 16281933
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  • 12. [Morphological studies of erythrocytes in congenital dyserythropoietic anemia type II].
    Koehler M, Schmidt-Riese L, Brandeis WE.
    Acta Haematol Pol; 1990 Nov 27; 21(2):144-52. PubMed ID: 2131714
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  • 13. [Congenital dyserythropoietic anemia type II: a case report and literature review].
    Li Y, Zhao X, Zhou K, Li Y, Li JP, Ye L, Peng GX, Fan HH, Jing LP, Zhang L, Zhang FK.
    Zhonghua Xue Ye Xue Za Zhi; 2012 Apr 27; 33(4):270-3. PubMed ID: 22781715
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  • 16. Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.
    Bianchi P, Fermo E, Vercellati C, Boschetti C, Barcellini W, Iurlo A, Marcello AP, Righetti PG, Zanella A.
    Hum Mutat; 2009 Sep 27; 30(9):1292-8. PubMed ID: 19621418
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  • 17. 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 Sep 27; 47(3):773-9. PubMed ID: 11310976
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  • 18. 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 27; 92(3):427-8. PubMed ID: 17339199
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  • 19. Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II).
    Iolascon A, Miraglia del Giudice E, Perrotta S, Granatiero M, Zelante L, Gasparini P.
    Blood; 1997 Nov 15; 90(10):4197-200. PubMed ID: 9354691
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  • 20. [Favorable effect of splenectomy on anemia in 3 siblings with type II congenital dyserythropoietic anemia (HEMPAS). (Ultrastructural changes in erythrocytes after splenectomy)].
    Chrobák L, Spacek J.
    Vnitr Lek; 1997 Oct 15; 43(10):635-8. PubMed ID: 9601875
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