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Journal Abstract Search

162 related items for PubMed ID: 31900952

  • 1. Congenital dyserythropoietic anaemia type I with nails and bone abnormalities.
    García-Zamora E, Naz-Villalba E, Pampín-Franco A, García-Iñigo FJ, López-Estebaranz JL.
    Clin Exp Dermatol; 2020 Jun; 45(4):515-517. PubMed ID: 31900952
    [No Abstract] [Full Text] [Related]

  • 2. Congenital dyserythropoietic anemia in China: a case report from two families and a review.
    Ru Y, Liu G, Bai J, Dong S, Nie N, Zhang H, Zhao S, Zheng Y, Zhu X, Nie G, Zhang F, Eyden B.
    Ann Hematol; 2014 May; 93(5):773-7. PubMed ID: 24196372
    [Abstract] [Full Text] [Related]

  • 3. Congenital dyserythropoietic anemia type III.
    Sandström H, Wahlin A.
    Haematologica; 2000 Jul; 85(7):753-7. PubMed ID: 10897128
    [Abstract] [Full Text] [Related]

  • 4. Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene.
    Ru YX, Zhu XF, Yan WW, Gao JT, Schwarz K, Heimpel H.
    Ann Hematol; 2008 Sep; 87(9):751-4. PubMed ID: 18575862
    [Abstract] [Full Text] [Related]

  • 5. A Very Rare Congenital Dyserythropoietic Anemia Variant-Type IV in a Patient With a Novel Mutation in the KLF1 Gene: A Case Report and Review of the Literature.
    Belgemen-Ozer T, Gorukmez O.
    J Pediatr Hematol Oncol; 2020 Aug; 42(6):e536-e540. PubMed ID: 32032242
    [Abstract] [Full Text] [Related]

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

  • 7. Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts.
    Renella R, Roberts NA, Brown JM, De Gobbi M, Bird LE, Hassanali T, Sharpe JA, Sloane-Stanley J, Ferguson DJ, Cordell J, Buckle VJ, Higgs DR, Wood WG.
    Blood; 2011 Jun 23; 117(25):6928-38. PubMed ID: 21364188
    [Abstract] [Full Text] [Related]

  • 8. Distal limb anomalies in patients with congenital dyserythropoietic anemia.
    Amir AZ, Horev G, Yacobovich J, Bennett M, Tamary H.
    Am J Med Genet A; 2017 Feb 23; 173(2):487-490. PubMed ID: 27759939
    [Abstract] [Full Text] [Related]

  • 9. Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene.
    Demircioğlu F, Erkoçoğlu M, Dilek M, Bekdaş M, Göksügür S, Büyükkorkmaz S, Açar S.
    Turk J Haematol; 2015 Sep 23; 32(3):283-4. PubMed ID: 25912935
    [No Abstract] [Full Text] [Related]

  • 10. Transduction with BBF2H7/CREB3L2 upregulates SEC23A protein in erythroblasts and partially corrects the hypo-glycosylation phenotype associated with CDAII.
    Pellegrin S, Haydn-Smith KL, Hampton-O'Neil LA, Hawley BR, Heesom KJ, Fermo E, Bianchi P, Toye AM.
    Br J Haematol; 2019 Mar 23; 184(5):876-881. PubMed ID: 29536501
    [No Abstract] [Full Text] [Related]

  • 11. KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity.
    Ravindranath Y, Johnson RM, Goyette G, Buck S, Gadgeel M, Gallagher PG.
    J Pediatr Hematol Oncol; 2018 Aug 23; 40(6):e405-e409. PubMed ID: 29300242
    [Abstract] [Full Text] [Related]

  • 12. Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A → G mutation, and pseudo-Gaucher cells in two siblings.
    Sharma P, Das R, Bansal D, Trehan A.
    Hematology; 2015 Mar 23; 20(2):104-7. PubMed ID: 24801240
    [Abstract] [Full Text] [Related]

  • 13. The diagnostic challenge of congenital dyserythropoietic anaemia: two cases of 'CDA type II'.
    Dukka S, King MJ, Hill QA.
    J Clin Pathol; 2014 Apr 23; 67(4):367-9. PubMed ID: 24385490
    [Abstract] [Full Text] [Related]

  • 14. Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II.
    Iolascon A, Delaunay J.
    Haematologica; 2009 May 23; 94(5):599-602. PubMed ID: 19407313
    [Abstract] [Full Text] [Related]

  • 15. 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 23; 85(9):591-5. PubMed ID: 16767397
    [Abstract] [Full Text] [Related]

  • 16. Non-haematological traits associated with congenital dyserythropoietic anaemia type 1: a new entity emerging.
    Sabry MA, Zaki M, al Awadi SA, al Saleh Q, Mattar MS.
    Clin Dysmorphol; 1997 Jul 23; 6(3):205-12. PubMed ID: 9220189
    [Abstract] [Full Text] [Related]

  • 17. Neonatal manifestations of congenital dyserythropoietic anemia type I.
    Shalev H, Tamary H, Shaft D, Reznitsky P, Zaizov R.
    J Pediatr; 1997 Jul 23; 131(1 Pt 1):95-7. PubMed ID: 9255198
    [Abstract] [Full Text] [Related]

  • 18. 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 23; 80(3):271-4. PubMed ID: 18081704
    [Abstract] [Full Text] [Related]

  • 19. Congenital dyserythropoietic anemia type II in a newborn with a novel compound heterozygous mutation in the SEC23B: a case report and review of the literature.
    Zheng J, Gao L, Liu H, Xiao P, Lu J, Li J, Wu S, Cheng S, Bian X, Du Z, Kong L, Hu S, Fan J.
    Int J Hematol; 2024 Feb 23; 119(2):210-214. PubMed ID: 38127226
    [Abstract] [Full Text] [Related]

  • 20. A novel variant mutation for congenital dyserythropoietic anemia, type II.
    Song JY, Pawar A, Collins C.
    Blood Cells Mol Dis; 2014 Dec 23; 53(4):272-3. PubMed ID: 24801741
    [No Abstract] [Full Text] [Related]

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