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Journal Abstract Search

404 related items for PubMed ID: 16281933

  • 21. [Atypical congenital dyserythropoietic anemia].
    Schmidt U, Richter HJ, Samandari S.
    Schweiz Med Wochenschr; 1987 Nov 07; 117(45):1776-80. PubMed ID: 3423766
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  • 22. [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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  • 23. Congenital dyserythropoietic anemia type III.
    Sandström H, Wahlin A.
    Haematologica; 2000 Jul 27; 85(7):753-7. PubMed ID: 10897128
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  • 24. Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous Arg1042Trp mutation in codanin-1).
    Tamary H, Offret H, Dgany O, Foliguet B, Wickramasinghe SN, Krasnov T, Rumilly F, Goujard C, Fénéant-Thibault M, Cynober T, Delaunay J.
    Eur J Haematol; 2008 Mar 27; 80(3):271-4. PubMed ID: 18081704
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  • 25. Ineffective erythropoiesis underlies the clinical heterogeneity of congenital dyserythropoietic anemia type II (CDA II).
    Kostaridou S, Polychronopoulou S, Premetis E, Papassotiriou I, Stamoulakatou A, Haidas S.
    Pediatr Int; 2004 Jun 27; 46(3):274-9. PubMed ID: 15151542
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  • 27. [Congenital dyserythropoietic anemia type III. A case report].
    Holm T, Kildahl-Andersen O, Sjo M.
    Tidsskr Nor Laegeforen; 1997 May 20; 117(13):1898-9. PubMed ID: 9214009
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  • 30. Ultrastructural, cell culture and karyotype study of bone marrow in a patient with congenital dyserythropoietic anaemia (CDA)-type III presenting with recurrent still-births.
    Ghosh K, Yavagal D, Phillips C, Jijina F, Pathare AV, Kerketta L, Iyer YS, Nair CN, Shinde S, Mohanty D.
    Haematologia (Budap); 1998 May 20; 29(1):41-5. PubMed ID: 9704256
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  • 31. The congenital dyserythropoietic anemias.
    Renella R, Wood WG.
    Hematol Oncol Clin North Am; 2009 Apr 20; 23(2):283-306. PubMed ID: 19327584
    [Abstract] [Full Text] [Related]

  • 32. Congenital dyserythropoietic anemias: a still unsolved puzzle.
    Iolascon A.
    Haematologica; 2000 Jul 20; 85(7):673-4. PubMed ID: 10897116
    [No Abstract] [Full Text] [Related]

  • 33. Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations.
    Meznarich JA, Draper L, Christensen RD, Yaish HM, Luem ND, Pysher TJ, Jung G, Nemeth E, Ganz T, Ward DM.
    Blood Cells Mol Dis; 2018 Jul 20; 71():63-66. PubMed ID: 29599085
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