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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 2
1980 2
1982 2
1983 1
1987 1
1989 2
1990 2
1992 1
1993 1
1995 1
1996 3
1997 6
1998 4
1999 4
2000 9
2001 3
2002 3
2003 4
2004 3
2005 2
2006 4
2007 2
2008 3
2009 2
2010 1
2011 1
2012 1
2014 2
2015 1
2016 2
2017 3
2018 4
2019 2
2020 4
2021 2
2022 1
2024 0

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Similar articles for PMID: 9354691

84 results

Results by year

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Page 1
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. Méndez M, et al. Ann Hematol. 2021 Feb;100(2):353-364. doi: 10.1007/s00277-020-04319-5. Epub 2020 Nov 7. Ann Hematol. 2021. PMID: 33159567
Genetic and functional insights into CDA-I prevalence and pathogenesis.
Olijnik AA, Roy NBA, Scott C, Marsh JA, Brown J, Lauschke K, Ask K, Roberts N, Downes DJ, Brolih S, Johnson E, Xella B, Proven M, Hipkiss R, Ryan K, Frisk P, Mäkk J, Stattin EM, Sadasivam N, McIlwaine L, Hill QA, Renella R, Hughes JR, Gibbons RJ, Groth A, McHugh PJ, Higgs DR, Buckle VJ, Babbs C. Olijnik AA, et al. J Med Genet. 2021 Mar;58(3):185-195. doi: 10.1136/jmedgenet-2020-106880. Epub 2020 Jun 9. J Med Genet. 2021. PMID: 32518175 Free PMC article.
KLF1 mutation E325K induces cell cycle arrest in erythroid cells differentiated from congenital dyserythropoietic anemia patient-specific induced pluripotent stem cells.
Kohara H, Utsugisawa T, Sakamoto C, Hirose L, Ogawa Y, Ogura H, Sugawara A, Liao J, Aoki T, Iwasaki T, Asai T, Doisaki S, Okuno Y, Muramatsu H, Abe T, Kurita R, Miyamoto S, Sakuma T, Shiba M, Yamamoto T, Ohga S, Yoshida K, Ogawa S, Ito E, Kojima S, Kanno H, Tani K. Kohara H, et al. Exp Hematol. 2019 May;73:25-37.e8. doi: 10.1016/j.exphem.2019.03.001. Epub 2019 Mar 12. Exp Hematol. 2019. PMID: 30876823 Free article. Clinical Trial.
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. Moreno-Carralero MI, et al. Eur J Haematol. 2018 Sep;101(3):368-378. doi: 10.1111/ejh.13112. Epub 2018 Jul 27. Eur J Haematol. 2018. PMID: 29901818
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. Aydin Koker S, et al. J Pediatr Hematol Oncol. 2018 Oct;40(7):e421-e423. doi: 10.1097/MPH.0000000000001207. J Pediatr Hematol Oncol. 2018. PMID: 29846281
84 results