190 related articles for article (PubMed ID: 19327584)
21. 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
Eur J Haematol; 2010 Jul; 85(1):20-5. PubMed ID: 20665989
[TBL] [Abstract][Full Text] [Related]
22. Lethal hydrops fetalis due to congenital dyserythropoietic anemia in a newborn: association of a new skeletal abnormality.
Tekinalp G; Sarici SU; Erdinç AS; Gögüş S; Balci S; Gürgey A
Pediatr Hematol Oncol; 2001 Dec; 18(8):537-42. PubMed ID: 11764104
[TBL] [Abstract][Full Text] [Related]
23. The congenital dyserythropoietic anaemias.
Delaunay J; Iolascon A
Baillieres Best Pract Res Clin Haematol; 1999 Dec; 12(4):691-705. PubMed ID: 10895259
[TBL] [Abstract][Full Text] [Related]
24. Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations.
Meznarich JA; Draper L; Christensen RD; Yaish HM; Luem ND; Pysher TJ; Jung G; Nemeth E; Ganz T; Ward DM
Blood Cells Mol Dis; 2018 Jul; 71():63-66. PubMed ID: 29599085
[TBL] [Abstract][Full Text] [Related]
25. Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic Anemia.
Aydin Koker S; Karapinar TH; Oymak Y; Bianchi P; Fermo E; Gozmen S; Vergin C
J Pediatr Hematol Oncol; 2018 Oct; 40(7):e421-e423. PubMed ID: 29846281
[TBL] [Abstract][Full Text] [Related]
26. Successful management of transfusion-dependent congenital dyserythropoietic anemia type 1b with interferon alfa-2a.
Rathe M; Møller MB; Greisen PW; Fisker N
Pediatr Blood Cancer; 2018 Mar; 65(3):. PubMed ID: 29049846
[TBL] [Abstract][Full Text] [Related]
27. Morbidity and mortality of adult patients with congenital dyserythropoietic anemia type I.
Shalev H; Al-Athamen K; Levi I; Levitas A; Tamary H
Eur J Haematol; 2017 Jan; 98(1):13-18. PubMed ID: 27206021
[TBL] [Abstract][Full Text] [Related]
28. Progress in the congenital dyserythropoietic anemias: juicy but high-hanging fruits?
Renella R
Am J Hematol; 2010 Dec; 85(12):913-4. PubMed ID: 21108324
[No Abstract] [Full Text] [Related]
29. Successful treatment of iron overload with phlebotomies in two siblings with congenital dyserythropoietic anemia--type II (CDA-II).
Chrobák L
Acta Medica (Hradec Kralove); 2006; 49(3):193-5. PubMed ID: 17117609
[TBL] [Abstract][Full Text] [Related]
30. Congenital dyserythropoietic anaemia type II: a rare entity.
Alam K; Aziz M; Varshney M; Maheshwari V; Basha M; Gaur K
BMJ Case Rep; 2011 Apr; 2011():. PubMed ID: 22696622
[TBL] [Abstract][Full Text] [Related]
31. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.
Arnaud L; Saison C; Helias V; Lucien N; Steschenko D; Giarratana MC; Prehu C; Foliguet B; Montout L; de Brevern AG; Francina A; Ripoche P; Fenneteau O; Da Costa L; Peyrard T; Coghlan G; Illum N; Birgens H; Tamary H; Iolascon A; Delaunay J; Tchernia G; Cartron JP
Am J Hum Genet; 2010 Nov; 87(5):721-7. PubMed ID: 21055716
[TBL] [Abstract][Full Text] [Related]
32. Distal limb anomalies in patients with congenital dyserythropoietic anemia.
Amir AZ; Horev G; Yacobovich J; Bennett M; Tamary H
Am J Med Genet A; 2017 Feb; 173(2):487-490. PubMed ID: 27759939
[TBL] [Abstract][Full Text] [Related]
33. [Congenital dyserythropoietic anemia type II: a case report and literature review].
Li Y; Zhao X; Zhou K; Li Y; Li JP; Ye L; Peng GX; Fan HH; Jing LP; Zhang L; Zhang FK
Zhonghua Xue Ye Xue Za Zhi; 2012 Apr; 33(4):270-3. PubMed ID: 22781715
[TBL] [Abstract][Full Text] [Related]
34. Congenital dyserythropoietic anemia in China: a case report from two families and a review.
Ru Y; Liu G; Bai J; Dong S; Nie N; Zhang H; Zhao S; Zheng Y; Zhu X; Nie G; Zhang F; Eyden B
Ann Hematol; 2014 May; 93(5):773-7. PubMed ID: 24196372
[TBL] [Abstract][Full Text] [Related]
35. Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemia.
Fargion S; Valenti L; Fracanzani AL; Sampietro M; Cappellini MD; Scaccabarozzi A; Soligo D; Mariani C; Fiorelli G
Blood; 2000 Nov; 96(10):3653-5. PubMed ID: 11071669
[TBL] [Abstract][Full Text] [Related]
36. A Very Rare Congenital Dyserythropoietic Anemia Variant-Type IV in a Patient With a Novel Mutation in the KLF1 Gene: A Case Report and Review of the Literature.
Belgemen-Ozer T; Gorukmez O
J Pediatr Hematol Oncol; 2020 Aug; 42(6):e536-e540. PubMed ID: 32032242
[TBL] [Abstract][Full Text] [Related]
37. Successful hematopoietic stem cell transplantation in a patient with congenital dyserythropoietic anemia type II.
Unal S; Russo R; Gumruk F; Kuskonmaz B; Cetin M; Sayli T; Tavil B; Langella C; Iolascon A; Uckan Cetinkaya D
Pediatr Transplant; 2014 Jun; 18(4):E130-3. PubMed ID: 24724984
[TBL] [Abstract][Full Text] [Related]
38. Tissue iron evaluation in chronically transfused children shows significant levels of iron loading at a very young age.
Berdoukas V; Nord A; Carson S; Puliyel M; Hofstra T; Wood J; Coates TD
Am J Hematol; 2013 Nov; 88(11):E283-5. PubMed ID: 23861216
[TBL] [Abstract][Full Text] [Related]
39. Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias.
Russo R; Iolascon A; Andolfo I; Marra R; Rosato BE
Int J Lab Hematol; 2024 May; ():. PubMed ID: 38747503
[TBL] [Abstract][Full Text] [Related]
40. Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: review of all reported cases and development of a clinical diagnostic paradigm.
Jaffray JA; Mitchell WB; Gnanapragasam MN; Seshan SV; Guo X; Westhoff CM; Bieker JJ; Manwani D
Blood Cells Mol Dis; 2013 Aug; 51(2):71-5. PubMed ID: 23522491
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
