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Items: 7

1.

Morbidity and mortality of adult patients with congenital dyserythropoietic anemia type I.

Shalev H, Al-Athamen K, Levi I, Levitas A, Tamary H.

Eur J Haematol. 2017 Jan;98(1):13-18. doi: 10.1111/ejh.12778. Epub 2016 Jun 15.

PMID:
27206021
2.

Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension with pigeon chest deformity.

El-Sheikh AA, Hashem H, Holman C, Vyas YM.

Pediatr Blood Cancer. 2014 Aug;61(8):1460-2. doi: 10.1002/pbc.24945. Epub 2014 Jan 13.

PMID:
24420417
3.

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
4.

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.

5.

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.

6.

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
7.

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.

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