163 related articles for article (PubMed ID: 20442439)
21. Congenital dyserythropoietic anaemia type I with nails and bone abnormalities.
García-Zamora E; Naz-Villalba E; Pampín-Franco A; García-Iñigo FJ; López-Estebaranz JL
Clin Exp Dermatol; 2020 Jun; 45(4):515-517. PubMed ID: 31900952
[No Abstract] [Full Text] [Related]
22. Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene.
Ru YX; Zhu XF; Yan WW; Gao JT; Schwarz K; Heimpel H
Ann Hematol; 2008 Sep; 87(9):751-4. PubMed ID: 18575862
[TBL] [Abstract][Full Text] [Related]
23. 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. PubMed ID: 23065504
[TBL] [Abstract][Full Text] [Related]
24. [Congenital dyserythropoietic anemia: types I and II. Study of 2 cases].
Luño E; Jonte F; Sánchez-San Román F; Rojo JM
Sangre (Barc); 1985; 30(1):37-46. PubMed ID: 4002097
[No Abstract] [Full Text] [Related]
25. Long-term cinemicrography of erythroblasts from a patient with congenital dyserythropoietic anemia type III: direct observation of dysplastic erythroblast formation.
Furukawa T; Inoue H; Sugita K; Eguchi M; Sakakibara H; Sugiyama S; Suda T
Blood Cells; 1993; 19(2):493-506; discussion 507-8. PubMed ID: 8312576
[TBL] [Abstract][Full Text] [Related]
26. Congenital dyserythropoietic anemia type I: report of a pair of siblings in Japan.
Kuribayashi T; Uchida S; Kuroume T; Umegae S; Omine M; Maekawa T
Blut; 1979 Sep; 39(3):201-9. PubMed ID: 476312
[TBL] [Abstract][Full Text] [Related]
27. Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis.
Fukuda MN
Baillieres Clin Haematol; 1993 Jun; 6(2):493-511. PubMed ID: 8043936
[TBL] [Abstract][Full Text] [Related]
28. Congenital dyserythropoietic anemia type II: serologic and morphologic family study.
Ricci P; Baccarani M; Biagini G; Preda P; Tomasini I; Zucchelli P; Tura S
Nouv Rev Fr Hematol (1978); 1979; 21(2):197-207. PubMed ID: 514807
[TBL] [Abstract][Full Text] [Related]
29. Congenital dyserythropoietic anemia type I. Report of a case.
Woessner S; Pardo P; Lafuente R; Feliu E; Vives JL; Sans-Sabrafen J
Blut; 1981 Jan; 42(1):47-52. PubMed ID: 7214028
[TBL] [Abstract][Full Text] [Related]
30. Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A → G mutation, and pseudo-Gaucher cells in two siblings.
Sharma P; Das R; Bansal D; Trehan A
Hematology; 2015 Mar; 20(2):104-7. PubMed ID: 24801240
[TBL] [Abstract][Full Text] [Related]
31. Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene.
Russo R; Marra R; Andolfo I; Manna F; De Rosa G; Rosato BE; Radhakrishnan K; Fahey M; Iolascon A
Am J Hematol; 2020 Nov; 95(11):1423-1426. PubMed ID: 32720728
[No Abstract] [Full Text] [Related]
32. Erythroblast multinuclearity in bone marrow and spleen. Congenital dyserythropoietic anemia-like abnormalities without functional evidence of dyserythropoiesis.
Lillicrap DP; Corbett WE; Giles AR; Ginsburg AD
Arch Pathol Lab Med; 1987 Jun; 111(6):536-9. PubMed ID: 3579510
[TBL] [Abstract][Full Text] [Related]
33. Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis.
Resnitzky P; Shaft D; Shalev H; Kapelushnik J; Dgany O; Krasnov T; Tamary H
Eur J Haematol; 2017 Oct; 99(4):366-371. PubMed ID: 28755517
[TBL] [Abstract][Full Text] [Related]
34. Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapy.
Goede JS; Benz R; Fehr J; Schwarz K; Heimpel H
Ann Hematol; 2006 Sep; 85(9):591-5. PubMed ID: 16767397
[TBL] [Abstract][Full Text] [Related]
35. Congenital dyserythropoietic anaemia.
Prasher N; Prasher BS
J Assoc Physicians India; 1989 Jul; 37(7):467-8. PubMed ID: 2613664
[TBL] [Abstract][Full Text] [Related]
36. Congenital dyserytropoietic anaemia, type II (HEMPAS) in three siblings.
Chrobák L; Radochová D; Smetana K; Matĕja F; Kout M; Polák J; Dítĕ P; Pribroský J; Dvorácková I
Folia Haematol Int Mag Klin Morphol Blutforsch; 1980; 107(4):628-40. PubMed ID: 6162730
[TBL] [Abstract][Full Text] [Related]
37. [Diagnosis and genetics of congenital dyserythropoietic anemias (CDA)].
Rössler J; Havers W
Klin Padiatr; 2000; 212(4):153-8. PubMed ID: 10994542
[TBL] [Abstract][Full Text] [Related]
38. Unclassified type of congenital dyserythropoietic anaemia (CDA) with prominent peripheral erythroblastosis.
Bethlenfalvay NC; Hadnagy C; Heimpel H
Br J Haematol; 1985 Jul; 60(3):541-50. PubMed ID: 4015990
[TBL] [Abstract][Full Text] [Related]
39. Congenital dyserythropoietic anaemias: new acquisitions.
Iolascon A; Russo R; Esposito MR; Piscopo C; Asci R; De Falco L; Di Noce F
Blood Transfus; 2011 Jul; 9(3):278-80. PubMed ID: 21251457
[No Abstract] [Full Text] [Related]
40. Congenital dyserythropoietic anemias.
Wickramasinghe SN
Curr Opin Hematol; 2000 Mar; 7(2):71-8. PubMed ID: 10698292
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
