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Journal Abstract Search

207 related items for PubMed ID: 8571938

  • 1. Congenital dyserythropoietic anemias.
    Marks PW, Mitus AJ.
    Am J Hematol; 1996 Jan; 51(1):55-63. PubMed ID: 8571938
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  • 2. 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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  • 3. 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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  • 9. Lethal hydrops fetalis due to congenital dyserythropoietic anemia in a newborn: association of a new skeletal abnormality.
    Tekinalp G, Sarici SU, Erdinç AS, Gögüş S, Balci S, Gürgey A.
    Pediatr Hematol Oncol; 2001 Dec; 18(8):537-42. PubMed ID: 11764104
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  • 12. [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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  • 13. Diagnosis and management of congenital dyserythropoietic anemias.
    Gambale A, Iolascon A, Andolfo I, Russo R.
    Expert Rev Hematol; 2016 Mar 07; 9(3):283-96. PubMed ID: 26653117
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  • 14. Congenital dyserythropoietic anemias.
    Iolascon A, Andolfo I, Russo R.
    Blood; 2020 Sep 10; 136(11):1274-1283. PubMed ID: 32702750
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  • 15. Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management.
    Risinger M, Emberesh M, Kalfa TA.
    Hematol Oncol Clin North Am; 2019 Jun 10; 33(3):373-392. PubMed ID: 31030808
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  • 16. The diagnostic challenge of congenital dyserythropoietic anaemia: two cases of 'CDA type II'.
    Dukka S, King MJ, Hill QA.
    J Clin Pathol; 2014 Apr 10; 67(4):367-9. PubMed ID: 24385490
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  • 17. Congenital dyserythropoietic anemias: a still unsolved puzzle.
    Iolascon A.
    Haematologica; 2000 Jul 10; 85(7):673-4. PubMed ID: 10897116
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  • 18. Variants of congenital dyserythropoietic anaemia: an update.
    Boogaerts MA, Verwilghen RL.
    Haematologia (Budap); 1982 Jul 10; 15(2):211-9. PubMed ID: 6761240
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  • 19. 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 10; 85(9):591-5. PubMed ID: 16767397
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  • 20. Congenital dyserythropoietic anemias: molecular insights and diagnostic approach.
    Iolascon A, Heimpel H, Wahlin A, Tamary H.
    Blood; 2013 Sep 26; 122(13):2162-6. PubMed ID: 23940284
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