354 related articles for article (PubMed ID: 29846281)
1. 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]
2. 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]
3. 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]
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. Identification of a novel splice variant in
Jang W; Ha DJ; Nahm CH; Park J; Kim SJ; Lee JE; Moon Y
Hematology; 2024 Dec; 29(1):2343163. PubMed ID: 38655690
[TBL] [Abstract][Full Text] [Related]
6. Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in the CDIN1 gene and functional study of a novel variant in the KIF23 gene.
Méndez M; Moreno-Carralero MI; Peri VL; Camacho-Galán R; Bosch-Benítez JM; Huerta-Aragonés J; Sánchez-Calero-Guilarte J; Moreno-Risco MB; Alonso-Domínguez JM; Morán-Jiménez MJ
Ann Hematol; 2021 Feb; 100(2):353-364. PubMed ID: 33159567
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12.
Alam MJ; Mandal AK; Mandal S; Jana JK
BMJ Case Rep; 2022 Jul; 15(7):. PubMed ID: 35820731
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. [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]
16. [Analysis of genotype and phenotype of SEC23B gene in a family affected with congenital dyserythropoietic anemia type II].
Li D; Li B; Qu S; Cao W; Yang Y; Ma Y; Hou T
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):874-878. PubMed ID: 29188620
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]