197 related articles for article (PubMed ID: 21378561)
1. Congenital dyserythropoietic anemias.
Iolascon A; Russo R; Delaunay J
Curr Opin Hematol; 2011 May; 18(3):146-51. PubMed ID: 21378561
[TBL] [Abstract][Full Text] [Related]
2. Congenital dyserythropoietic anemias: molecular insights and diagnostic approach.
Iolascon A; Heimpel H; Wahlin A; Tamary H
Blood; 2013 Sep; 122(13):2162-6. PubMed ID: 23940284
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Clinical and genetic features of congenital dyserythropoietic anemia (CDA).
Moreno-Carralero MI; Horta-Herrera S; Morado-Arias M; Ricard-Andrés MP; Lemes-Castellano A; Abio-Calvete M; Cedena-Romero MT; González-Fernández FA; Llorente-González L; Periago-Peralta AM; de-la-Iglesia-Íñigo S; Méndez M; Morán-Jiménez MJ
Eur J Haematol; 2018 Sep; 101(3):368-378. PubMed ID: 29901818
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Congenital dyserythropoietic anemia.
Kamiya T; Manabe A
Int J Hematol; 2010 Oct; 92(3):432-8. PubMed ID: 20820969
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. [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]
10. The congenital dyserythropoieitic anemias: genetics and pathophysiology.
King R; Gallagher PJ; Khoriaty R
Curr Opin Hematol; 2022 May; 29(3):126-136. PubMed ID: 35441598
[TBL] [Abstract][Full Text] [Related]
11. Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.
Schwarz K; Iolascon A; Verissimo F; Trede NS; Horsley W; Chen W; Paw BH; Hopfner KP; Holzmann K; Russo R; Esposito MR; Spano D; De Falco L; Heinrich K; Joggerst B; Rojewski MT; Perrotta S; Denecke J; Pannicke U; Delaunay J; Pepperkok R; Heimpel H
Nat Genet; 2009 Aug; 41(8):936-40. PubMed ID: 19561605
[TBL] [Abstract][Full Text] [Related]
12. Congenital dyserythropoietic anemia type II in a newborn with a novel compound heterozygous mutation in the SEC23B: a case report and review of the literature.
Zheng J; Gao L; Liu H; Xiao P; Lu J; Li J; Wu S; Cheng S; Bian X; Du Z; Kong L; Hu S; Fan J
Int J Hematol; 2024 Feb; 119(2):210-214. PubMed ID: 38127226
[TBL] [Abstract][Full Text] [Related]
13. Congenital dyserythropoietic anemias: epidemiology, clinical significance, and progress in understanding their pathogenesis.
Heimpel H
Ann Hematol; 2004 Oct; 83(10):613-21. PubMed ID: 15278299
[TBL] [Abstract][Full Text] [Related]
14. Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts.
Renella R; Roberts NA; Brown JM; De Gobbi M; Bird LE; Hassanali T; Sharpe JA; Sloane-Stanley J; Ferguson DJ; Cordell J; Buckle VJ; Higgs DR; Wood WG
Blood; 2011 Jun; 117(25):6928-38. PubMed ID: 21364188
[TBL] [Abstract][Full Text] [Related]
15. Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia.
Hamada M; Doisaki S; Okuno Y; Muramatsu H; Hama A; Kawashima N; Narita A; Nishio N; Yoshida K; Kanno H; Manabe A; Taga T; Takahashi Y; Miyano S; Ogawa S; Kojima S
Int J Hematol; 2018 Sep; 108(3):306-311. PubMed ID: 29936674
[TBL] [Abstract][Full Text] [Related]
16. The congenital dyserythropoietic anemias.
Renella R; Wood WG
Hematol Oncol Clin North Am; 2009 Apr; 23(2):283-306. PubMed ID: 19327584
[TBL] [Abstract][Full Text] [Related]
17. Identification of CDAN1, C15ORF41 and SEC23B mutations in Chinese patients affected by congenital dyserythropoietic anemia.
Wang Y; Ru Y; Liu G; Dong S; Li Y; Zhu X; Zhang F; Chang YZ; Nie G
Gene; 2018 Jan; 640():73-78. PubMed ID: 29031773
[TBL] [Abstract][Full Text] [Related]
18. Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia.
Fujino H; Doisaki S; Park YD; Hama A; Muramatsu H; Kojima S; Sumimoto S
Int J Hematol; 2013 May; 97(5):650-3. PubMed ID: 23605369
[TBL] [Abstract][Full Text] [Related]
19. Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management.
Risinger M; Emberesh M; Kalfa TA
Hematol Oncol Clin North Am; 2019 Jun; 33(3):373-392. PubMed ID: 31030808
[TBL] [Abstract][Full Text] [Related]
20. Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population.
Saptarshi AN; Dongerdiye RK; More TA; Kedar PS
Ital J Pediatr; 2023 Jul; 49(1):84. PubMed ID: 37455305
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
