216 related articles for article (PubMed ID: 29936674)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.
Russo R; Andolfo I; Manna F; Gambale A; Marra R; Rosato BE; Caforio P; Pinto V; Pignataro P; Radhakrishnan K; Unal S; Tomaiuolo G; Forni GL; Iolascon A
Am J Hematol; 2018 May; 93(5):672-682. PubMed ID: 29396846
[TBL] [Abstract][Full Text] [Related]
8. Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR).
Niss O; Lorsbach RB; Berger M; Chonat S; McLemore M; Buchbinder D; McCavit T; Shaffer LG; Simpson J; Schwartz JH; Meznarich J; Emberesh M; Seu KG; Zhang W; Kalfa TA;
Blood Cells Mol Dis; 2021 Mar; 87():102534. PubMed ID: 33401150
[TBL] [Abstract][Full Text] [Related]
9. Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II.
Chen S; Guo Z; Ye Y; Yang S; Huang G
Int J Hematol; 2021 Sep; 114(3):390-394. PubMed ID: 33914262
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
14. Congenital dyserythropoietic anemia type III.
Sandström H; Wahlin A
Haematologica; 2000 Jul; 85(7):753-7. PubMed ID: 10897128
[TBL] [Abstract][Full Text] [Related]
15. Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias.
Shefer Averbuch N; Steinberg-Shemer O; Dgany O; Krasnov T; Noy-Lotan S; Yacobovich J; Kuperman AA; Kattamis A; Ben Barak A; Roth-Jelinek B; Chubar E; Shabad E; Dufort G; Ellis M; Wolach O; Pazgal I; Abu Quider A; Miskin H; Tamary H
Eur J Haematol; 2018 Sep; 101(3):297-304. PubMed ID: 29786897
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. New Cases and Mutations in
Musri MM; Venturi V; Ferrer-Cortès X; Romero-Cortadellas L; Hernández G; Leoz P; Ricard Andrés MP; Morado M; Fernández Valle MDC; Beneitez Pastor D; Ortuño Cabrero A; Moreno Gamiz M; Senent Peris L; Perez-Valencia AI; Pérez-Montero S; Tornador C; Sánchez M
Int J Mol Sci; 2023 Jun; 24(12):. PubMed ID: 37373084
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Dyserythropoietic anemia].
Fereberger W
Acta Med Austriaca Suppl; 1979; 6():281-6. PubMed ID: 299214
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
