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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. Eur J Haematol. 2010 Jul;85(1):20-5. Eur J Haematol. 2010. PMID: 20665989
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis.
Tchernia G, Delhommeau F, Perrotta S, Cynober T, Bader-Meunier B, Nobili B, Rohrlich P, Salomon JL, Sagot-Bevenot S, del Giudice EM, Delaunay J, DeMattia D, Schischmanoff PO, Mohandas N, Iolascon A; ESPHI working group on hemolytic anemias. Tchernia G, et al. Hematol J. 2000;1(3):146-52. doi: 10.1038/sj.thj.6200022. Hematol J. 2000. PMID: 11920183
Congenital dyserythropoietic anemias.
Tchernia G, Bader-Meunier B, Beauchamp-Nicoud A, Cynober T, Fénéant-Thibault M, Delaunay J. Tchernia G, et al. Hematol J. 2004;5 Suppl 3:S191-4. doi: 10.1038/sj.thj.6200451. Hematol J. 2004. PMID: 15190307 Review. No abstract available.
Clinical and molecular variability in congenital dyserythropoietic anaemia type I.
Tamary H, Dgany O, Proust A, Krasnov T, Avidan N, Eidelitz-Markus T, Tchernia G, Geneviève D, Cormier-Daire V, Bader-Meunier B, Ferrero-Vacher C, Munzer M, Gruppo R, Fibach E, Konen O, Yaniv I, Delaunay J. Tamary H, et al. Br J Haematol. 2005 Aug;130(4):628-34. doi: 10.1111/j.1365-2141.2005.05642.x. Br J Haematol. 2005. PMID: 16098079 Free article.
307 results