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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: wickramasinghe sn. 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
Potentiation of erythroid abnormalities following macrophage depletion in aged rats.
Lisa Giuliani A, Graldi G, Veronesi M, Lorenzini F, Gandini G, Unis L, Previato A, Wiener E, Wickramasinghe SN, Berti G. Lisa Giuliani A, et al. Among authors: wickramasinghe sn. Eur J Haematol. 2007 Jan;78(1):72-81. doi: 10.1111/j.0902-4441.2006.t01-1-EJH3017.x. Epub 2006 Oct 17. Eur J Haematol. 2007. PMID: 17042771
Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.
Ahmed MR, Chehal A, Zahed L, Taher A, Haidar J, Shamseddine A, O'Hea AM, Bienz N, Dgany O, Avidan N, Beckmann JS, Tamary H, Higgs D, Vyas P, Wood WG, Wickramasinghe SN. Ahmed MR, et al. Among authors: wickramasinghe sn. Blood. 2006 Jun 15;107(12):4968-9. doi: 10.1182/blood-2006-01-0081. Blood. 2006. PMID: 16754775 Free article. No abstract available.
Diagnosis of megaloblastic anaemias.
Wickramasinghe SN. Wickramasinghe SN. Blood Rev. 2006 Nov;20(6):299-318. doi: 10.1016/j.blre.2006.02.002. Epub 2006 May 22. Blood Rev. 2006. PMID: 16716475 Review.
214 results