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Results: 10

1.

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. doi: 10.1007/s00277-013-1933-8. Epub 2013 Nov 7. Review.

PMID:
24196372
[PubMed - indexed for MEDLINE]
2.

Congenital dyserythropoietic anemias: molecular insights and diagnostic approach.

Iolascon A, Heimpel H, Wahlin A, Tamary H.

Blood. 2013 Sep 26;122(13):2162-6. doi: 10.1182/blood-2013-05-468223. Epub 2013 Aug 12. Review.

PMID:
23940284
[PubMed - indexed for MEDLINE]
3.

Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.

Babbs C, Roberts NA, Sanchez-Pulido L, McGowan SJ, Ahmed MR, Brown JM, Sabry MA; WGS500 Consortium, Bentley DR, McVean GA, Donnelly P, Gileadi O, Ponting CP, Higgs DR, Buckle VJ.

Haematologica. 2013 Sep;98(9):1383-7. doi: 10.3324/haematol.2013.089490. Epub 2013 May 28.

PMID:
23716552
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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;97(5):650-3. doi: 10.1007/s12185-013-1338-4. Epub 2013 Apr 19.

PMID:
23605369
[PubMed - indexed for MEDLINE]
5.

Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach.

Iolascon A, Esposito MR, Russo R.

Haematologica. 2012 Dec;97(12):1786-94. doi: 10.3324/haematol.2012.072207. Epub 2012 Oct 12. Review.

PMID:
23065504
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

A case of congenital dyserythropoietic anemia type 1 in a Japanese adult with a CDAN1 gene mutation and an inappropriately low serum hepcidin-25 level.

Kawabata H, Doisaki S, Okamoto A, Uchiyama T, Sakamoto S, Hama A, Hosoda K, Fujikura J, Kanno H, Fujii H, Tomosugi N, Nakao K, Kojima S, Takaori-Kondo A.

Intern Med. 2012;51(8):917-20. Epub 2012 Apr 15.

PMID:
22504250
[PubMed - indexed for MEDLINE]
Free Article
7.

Codanin-1, mutated in the anaemic disease CDAI, regulates Asf1 function in S-phase histone supply.

Ask K, Jasencakova Z, Menard P, Feng Y, Almouzni G, Groth A.

EMBO J. 2012 Apr 18;31(8):2013-23. doi: 10.1038/emboj.2012.55. Epub 2012 Mar 9. Erratum in: EMBO J. 2012 Jul 18;31(14):3229.

PMID:
22407294
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Congenital dyserythropoietic anemias.

Iolascon A, Russo R, Delaunay J.

Curr Opin Hematol. 2011 May;18(3):146-51. doi: 10.1097/MOH.0b013e32834521b0. Review.

PMID:
21378561
[PubMed - indexed for MEDLINE]
9.

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. doi: 10.1182/blood-2010-09-308478. Epub 2011 Mar 1.

PMID:
21364188
[PubMed - indexed for MEDLINE]
Free Article
10.

Congenital dyserythropoietic anemia.

Kamiya T, Manabe A.

Int J Hematol. 2010 Oct;92(3):432-8. doi: 10.1007/s12185-010-0667-9. Epub 2010 Sep 7.

PMID:
20820969
[PubMed - indexed for MEDLINE]

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