These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

224 related items for PubMed ID: 32702750

  • 1. Congenital dyserythropoietic anemias.
    Iolascon A, Andolfo I, Russo R.
    Blood; 2020 Sep 10; 136(11):1274-1283. PubMed ID: 32702750
    [Abstract] [Full Text] [Related]

  • 2. Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias.
    Russo R, Iolascon A, Andolfo I, Marra R, Rosato BE.
    Int J Lab Hematol; 2024 Aug 10; 46(4):595-605. PubMed ID: 38747503
    [Abstract] [Full Text] [Related]

  • 3. Diagnosis and management of congenital dyserythropoietic anemias.
    Gambale A, Iolascon A, Andolfo I, Russo R.
    Expert Rev Hematol; 2016 Mar 10; 9(3):283-96. PubMed ID: 26653117
    [Abstract] [Full Text] [Related]

  • 4. The congenital dyserythropoietic anemias.
    Renella R, Wood WG.
    Hematol Oncol Clin North Am; 2009 Apr 10; 23(2):283-306. PubMed ID: 19327584
    [Abstract] [Full Text] [Related]

  • 5. Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR).
    Niss O, Lorsbach RB, Berger M, Chonat S, McLemore M, Buchbinder D, McCavit T, Shaffer LG, Simpson J, Schwartz JH, Meznarich J, Emberesh M, Seu KG, Zhang W, Kalfa TA, CDAR consortium.
    Blood Cells Mol Dis; 2021 Mar 10; 87():102534. PubMed ID: 33401150
    [Abstract] [Full Text] [Related]

  • 6. Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic Anemia.
    Aydin Koker S, Karapinar TH, Oymak Y, Bianchi P, Fermo E, Gozmen S, Vergin C.
    J Pediatr Hematol Oncol; 2018 Oct 10; 40(7):e421-e423. PubMed ID: 29846281
    [Abstract] [Full Text] [Related]

  • 7. The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant.
    Andolfo I, Rosato BE, Marra R, De Rosa G, Manna F, Gambale A, Iolascon A, Russo R.
    Am J Hematol; 2019 Nov 10; 94(11):1227-1235. PubMed ID: 31400017
    [Abstract] [Full Text] [Related]

  • 8. An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations.
    Lee HH, Mak AS, Kou KO, Poon CF, Wong WS, Chiu KH, Au PK, Chan KY, Kan AS, Tang MH, Leung KY.
    Hemoglobin; 2016 Nov 10; 40(6):431-434. PubMed ID: 28361594
    [Abstract] [Full Text] [Related]

  • 9. Congenital dyserythropoietic anemias: epidemiology, clinical significance, and progress in understanding their pathogenesis.
    Heimpel H.
    Ann Hematol; 2004 Oct 10; 83(10):613-21. PubMed ID: 15278299
    [Abstract] [Full Text] [Related]

  • 10. Congenital dyserythropoietic anemias.
    Marks PW, Mitus AJ.
    Am J Hematol; 1996 Jan 10; 51(1):55-63. PubMed ID: 8571938
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. The congenital dyserythropoietic anaemias.
    Delaunay J, Iolascon A.
    Baillieres Best Pract Res Clin Haematol; 1999 Dec 10; 12(4):691-705. PubMed ID: 10895259
    [Abstract] [Full Text] [Related]

  • 14. Congenital dyserythropoietic anemias.
    Iolascon A, Russo R, Delaunay J.
    Curr Opin Hematol; 2011 May 10; 18(3):146-51. PubMed ID: 21378561
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Advances in the understanding of the congenital dyserythropoietic anaemias.
    Wickramasinghe SN, Wood WG.
    Br J Haematol; 2005 Nov 26; 131(4):431-46. PubMed ID: 16281933
    [Abstract] [Full Text] [Related]

  • 17. Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia.
    Fujino H, Doisaki S, Park YD, Hama A, Muramatsu H, Kojima S, Sumimoto S.
    Int J Hematol; 2013 May 26; 97(5):650-3. PubMed ID: 23605369
    [Abstract] [Full Text] [Related]

  • 18. 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 26; 18(8):537-42. PubMed ID: 11764104
    [Abstract] [Full Text] [Related]

  • 19. The diagnostic challenge of congenital dyserythropoietic anaemia: two cases of 'CDA type II'.
    Dukka S, King MJ, Hill QA.
    J Clin Pathol; 2014 Apr 26; 67(4):367-9. PubMed ID: 24385490
    [Abstract] [Full Text] [Related]

  • 20. The congenital dyserythropoieitic anemias: genetics and pathophysiology.
    King R, Gallagher PJ, Khoriaty R.
    Curr Opin Hematol; 2022 May 01; 29(3):126-136. PubMed ID: 35441598
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.