Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

554 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Frequency of congenital dyserythropoietic anemias in Europe.
Heimpel H, Matuschek A, Ahmed M, Bader-Meunier B, Colita A, Delaunay J, Garcon L, Gilsanz F, Goede J, Högel J, Kohne E, Leichtle R, Munoz J, Perrotta S, Piscopo C, Renella R, Schwarz K, Smolenska-Sym G, Wickramasinghe S, Zanella A, Iolascon A. Heimpel H, et al. Among authors: delaunay j. Eur J Haematol. 2010 Jul;85(1):20-5. Eur J Haematol. 2010. PMID: 20665989
The congenital dyserythropoietic anaemias.
Delaunay J, Iolascon A. Delaunay J, et al. Baillieres Best Pract Res Clin Haematol. 1999 Dec;12(4):691-705. doi: 10.1053/beha.1999.0048. Baillieres Best Pract Res Clin Haematol. 1999. PMID: 10895259 Review.
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. Schwarz K, et al. Among authors: delaunay j. Nat Genet. 2009 Aug;41(8):936-40. doi: 10.1038/ng.405. Epub 2009 Jun 28. Nat Genet. 2009. PMID: 19561605 Free article.
Congenital dyserythropoietic anemias.
Iolascon A, Russo R, Delaunay J. Iolascon A, et al. Among authors: delaunay j. Curr Opin Hematol. 2011 May;18(3):146-51. doi: 10.1097/MOH.0b013e32834521b0. Curr Opin Hematol. 2011. PMID: 21378561 Review.
Natural history of congenital dyserythropoietic anemia type II.
Iolascon A, Delaunay J, Wickramasinghe SN, Perrotta S, Gigante M, Camaschella C. Iolascon A, et al. Among authors: delaunay j. Blood. 2001 Aug 15;98(4):1258-60. doi: 10.1182/blood.v98.4.1258. Blood. 2001. PMID: 11493480 Free article.
Congenital dyserythropoietic anemias.
Tchernia G, Bader-Meunier B, Beauchamp-Nicoud A, Cynober T, Fénéant-Thibault M, Delaunay J. Tchernia G, et al. Among authors: delaunay j. Hematol J. 2004;5 Suppl 3:S191-4. doi: 10.1038/sj.thj.6200451. Hematol J. 2004. PMID: 15190307 Review. No abstract available.
Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.
Iolascon A, Russo R, Esposito MR, Asci R, Piscopo C, Perrotta S, Fénéant-Thibault M, Garçon L, Delaunay J. Iolascon A, et al. Among authors: delaunay j. Haematologica. 2010 May;95(5):708-15. doi: 10.3324/haematol.2009.014985. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015893 Free PMC article.
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. Tamary H, et al. Among authors: delaunay j. Eur J Haematol. 2008 Mar;80(3):271-4. doi: 10.1111/j.1600-0609.2007.01004.x. Epub 2007 Dec 7. Eur J Haematol. 2008. PMID: 18081704
554 results