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Journal Abstract Search

168 related items for PubMed ID: 9745888

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  • 23. Lethal congenital dyserythropoietic anaemia type I in siblings presenting as pericardial effusions in the second trimester.
    Stone P, Zuccollo J.
    Fetal Diagn Ther; 1999; 14(1):11-4. PubMed ID: 10072642
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  • 27. Congenital dyserythropoietic anemia type III.
    Sandström H, Wahlin A.
    Haematologica; 2000 Jul; 85(7):753-7. PubMed ID: 10897128
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  • 29. Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients.
    Marra R, Nostroso A, Rosato BE, Esposito FM, D'Onofrio V, Iscaro A, Gambale A, Bruschi B, Coccia P, Poloni A, Unal S, Romano A, Iolascon A, Andolfo I, Russo R.
    Am J Hematol; 2024 Aug; 99(8):1511-1522. PubMed ID: 38666530
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  • 32. Congenital dyserythropoietic anemia: clinical and hematological profile.
    Marwaha RK, Bansal D, Trehan A, Garewal G, Marwaha N.
    Indian Pediatr; 2003 Jun; 40(6):551-5. PubMed ID: 12824665
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  • 35. 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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  • 36. Congenital dyserythropoietic anemia type II: molecular basis and clinical aspects.
    Iolascon A, D'Agostaro G, Perrotta S, Izzo P, Tavano R, Miraglia del Giudice B.
    Haematologica; 1996 May; 81(6):543-59. PubMed ID: 9009444
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  • 37. 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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  • 38. Iron loading anaemias.
    Mehta BC, Pandya BG, Mehta JB, Bisariya BN.
    J Assoc Physicians India; 1989 Dec; 37(12):754-6. PubMed ID: 2636578
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