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For: Wickramasinghe SN. Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data. Blood Rev. 1998;12:178-200. [PMID: 9745888 DOI: 10.1016/s0268-960x(98)90016-9] [Cited by in Crossref: 58] [Cited by in F6Publishing: 9] [Article Influence: 2.6] [Reference Citation Analysis]
Number Citing Articles
1 Denecke J, Kranz C, Nimtz M, Conradt HS, Brune T, Heimpel H, Marquardt T. Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS). Glycoconj J 2008;25:375-82. [PMID: 18166993 DOI: 10.1007/s10719-007-9089-1] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 1.1] [Reference Citation Analysis]
2 Iolascon A, Esposito MR, Russo R. Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach. Haematologica 2012;97:1786-94. [PMID: 23065504 DOI: 10.3324/haematol.2012.072207] [Cited by in Crossref: 50] [Cited by in F6Publishing: 40] [Article Influence: 5.6] [Reference Citation Analysis]
3 Babbs C, Roberts NA, Sanchez-Pulido L, McGowan SJ, Ahmed MR, Brown JM, Sabry MA, Bentley DR, McVean GA, Donnelly P, Gileadi O, Ponting CP, Higgs DR, Buckle VJ; WGS500 Consortium. Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I. Haematologica 2013;98:1383-7. [PMID: 23716552 DOI: 10.3324/haematol.2013.089490] [Cited by in Crossref: 51] [Cited by in F6Publishing: 37] [Article Influence: 6.4] [Reference Citation Analysis]
4 Magor GW, Tallack MR, Gillinder KR, Bell CC, McCallum N, Williams B, Perkins AC. KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome. Blood 2015;125:2405-17. [PMID: 25724378 DOI: 10.1182/blood-2014-08-590968] [Cited by in Crossref: 57] [Cited by in F6Publishing: 41] [Article Influence: 9.5] [Reference Citation Analysis]
5 Satchwell TJ, Pellegrin S, Bianchi P, Hawley BR, Gampel A, Mordue KE, Budnik A, Fermo E, Barcellini W, Stephens DJ, van den Akker E, Toye AM. Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesis. Haematologica 2013;98:1788-96. [PMID: 23935019 DOI: 10.3324/haematol.2013.085522] [Cited by in Crossref: 30] [Cited by in F6Publishing: 22] [Article Influence: 3.8] [Reference Citation Analysis]
6 Iolascon A, Delaunay J. Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II. Haematologica 2009;94:599-602. [PMID: 19407313 DOI: 10.3324/haematol.2009.005785] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 0.8] [Reference Citation Analysis]
7 Roy NBA, Babbs C. The pathogenesis, diagnosis and management of congenital dyserythropoietic anaemia type I. Br J Haematol 2019;185:436-49. [PMID: 30836435 DOI: 10.1111/bjh.15817] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 8.5] [Reference Citation Analysis]
8 Heimpel H, Kellermann K, Neuschwander N, Högel J, Schwarz K. The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells. Haematologica 2010;95:1034-6. [PMID: 20421275 DOI: 10.3324/haematol.2009.014563] [Cited by in Crossref: 40] [Cited by in F6Publishing: 28] [Article Influence: 3.6] [Reference Citation Analysis]
9 Chirnomas SD, Kupfer GM. The inherited bone marrow failure syndromes. Pediatr Clin North Am 2013;60:1291-310. [PMID: 24237972 DOI: 10.1016/j.pcl.2013.09.007] [Cited by in Crossref: 30] [Cited by in F6Publishing: 15] [Article Influence: 4.3] [Reference Citation Analysis]