Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 110

1.

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
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.

3.

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.

Arnaud L, Saison C, Helias V, Lucien N, Steschenko D, Giarratana MC, Prehu C, Foliguet B, Montout L, de Brevern AG, Francina A, Ripoche P, Fenneteau O, Da Costa L, Peyrard T, Coghlan G, Illum N, Birgens H, Tamary H, Iolascon A, Delaunay J, Tchernia G, Cartron JP.

Am J Hum Genet. 2010 Nov 12;87(5):721-7. doi: 10.1016/j.ajhg.2010.10.010. Epub 2010 Nov 4.

4.

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.

5.

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
6.

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
7.

[Diagnosis and genetics of congenital dyserythropoietic anemias (CDA)].

Rössler J, Havers W.

Klin Padiatr. 2000 Jul-Aug;212(4):153-8. Review. German.

PMID:
10994542
8.

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

Schwarz K, Iolascon A, Verissimo F, Trede NS, Horsley W, Chen W, Paw BH, Hopfner KP, Holzmann K, Russo R, Esposito MR, Spano D, De Falco L, Heinrich K, Joggerst B, Rojewski MT, Perrotta S, Denecke J, Pannicke U, Delaunay J, Pepperkok R, Heimpel H.

Nat Genet. 2009 Aug;41(8):936-40. doi: 10.1038/ng.405. Epub 2009 Jun 28.

PMID:
19561605
9.
10.

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.

11.

The congenital dyserythropoietic anemias.

Renella R, Wood WG.

Hematol Oncol Clin North Am. 2009 Apr;23(2):283-306. doi: 10.1016/j.hoc.2009.01.010. Review.

PMID:
19327584
12.

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
13.

[Congenital dyserythropoietic anemia type II: a case report and literature review].

Li Y, Zhao X, Zhou K, Li Y, Li JP, Ye L, Peng GX, Fan HH, Jing LP, Zhang L, Zhang FK.

Zhonghua Xue Ye Xue Za Zhi. 2012 Apr;33(4):270-3. Review. Chinese.

PMID:
22781715
14.

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.

Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H.

Am J Hum Genet. 2002 Dec;71(6):1467-74. Epub 2002 Nov 14.

15.

Congenital dyserythropoietic anemias.

Wickramasinghe SN.

Curr Opin Hematol. 2000 Mar;7(2):71-8. Review.

PMID:
10698292
16.

The congenital dyserythropoietic anaemias.

Delaunay J, Iolascon A.

Baillieres Best Pract Res Clin Haematol. 1999 Dec;12(4):691-705. Review.

PMID:
10895259
17.

Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: review of all reported cases and development of a clinical diagnostic paradigm.

Jaffray JA, Mitchell WB, Gnanapragasam MN, Seshan SV, Guo X, Westhoff CM, Bieker JJ, Manwani D.

Blood Cells Mol Dis. 2013 Aug;51(2):71-5. doi: 10.1016/j.bcmd.2013.02.006. Epub 2013 Mar 20. Review.

18.

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;20(2):104-7. doi: 10.1179/1607845414Y.0000000166. Epub 2014 May 6.

PMID:
24801240
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;67(4):367-9. doi: 10.1136/jclinpath-2013-201779. Epub 2014 Jan 2.

PMID:
24385490
20.

Diagnosis and management of congenital dyserythropoietic anemias.

Gambale A, Iolascon A, Andolfo I, Russo R.

Expert Rev Hematol. 2016 Mar;9(3):283-96. doi: 10.1586/17474086.2016.1131608. Epub 2016 Jan 6. Review.

PMID:
26653117

Supplemental Content

Support Center