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

Year Number of Results
1979 2
1981 5
1982 3
1983 6
1985 2
1987 1
1988 1
1989 1
1991 3
1992 6
1993 7
1994 8
1995 7
1996 10
1997 15
1998 17
1999 19
2000 18
2001 8
2002 11
2003 9
2004 4
2005 7
2006 11
2007 13
2008 10
2009 13
2010 14
2011 15
2012 12
2013 12
2014 12
2015 11
2016 15
2017 19
2018 13
2019 18
2020 25
2021 15
2022 3
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Search Results

372 results
Results by year
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Page 1
Congenital dyserythropoietic anemias.
Iolascon A, Andolfo I, Russo R. Iolascon A, et al. Blood. 2020 Sep 10;136(11):1274-1283. doi: 10.1182/blood.2019000948. Blood. 2020. PMID: 32702750 Free article. Review.
Genetic Predisposition to Solid Pediatric Cancers.
Capasso M, Montella A, Tirelli M, Maiorino T, Cantalupo S, Iolascon A. Capasso M, et al. Among authors: iolascon a. Front Oncol. 2020 Oct 28;10:590033. doi: 10.3389/fonc.2020.590033. eCollection 2020. Front Oncol. 2020. PMID: 33194750 Free PMC article. Review.
Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
Bolton-Maggs PH, Langer JC, Iolascon A, Tittensor P, King MJ; General Haematology Task Force of the British Committee for Standards in Haematology. Bolton-Maggs PH, et al. Among authors: iolascon a. Br J Haematol. 2012 Jan;156(1):37-49. doi: 10.1111/j.1365-2141.2011.08921.x. Epub 2011 Nov 5. Br J Haematol. 2012. PMID: 22055020
Recommendations regarding splenectomy in hereditary hemolytic anemias.
Iolascon A, Andolfo I, Barcellini W, Corcione F, Garçon L, De Franceschi L, Pignata C, Graziadei G, Pospisilova D, Rees DC, de Montalembert M, Rivella S, Gambale A, Russo R, Ribeiro L, Vives-Corrons J, Martinez PA, Kattamis A, Gulbis B, Cappellini MD, Roberts I, Tamary H; Working Study Group on Red Cells and Iron of the EHA. Iolascon A, et al. Haematologica. 2017 Aug;102(8):1304-1313. doi: 10.3324/haematol.2016.161166. Epub 2017 May 26. Haematologica. 2017. PMID: 28550188 Free PMC article.
The pyruvate kinase activator mitapivat reduces hemolysis and improves anemia in a β-thalassemia mouse model.
Matte A, Federti E, Kung C, Kosinski PA, Narayanaswamy R, Russo R, Federico G, Carlomagno F, Desbats MA, Salviati L, Leboeuf C, Valenti MT, Turrini F, Janin A, Yu S, Beneduce E, Ronseaux S, Iatcenko I, Dang L, Ganz T, Jung CL, Iolascon A, Brugnara C, De Franceschi L. Matte A, et al. Among authors: iolascon a. J Clin Invest. 2021 May 17;131(10):e144206. doi: 10.1172/JCI144206. J Clin Invest. 2021. PMID: 33822774 Free PMC article.
Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19.
Andolfo I, Russo R, Lasorsa VA, Cantalupo S, Rosato BE, Bonfiglio F, Frisso G, Abete P, Cassese GM, Servillo G, Esposito G, Gentile I, Piscopo C, Villani R, Fiorentino G, Cerino P, Buonerba C, Pierri B, Zollo M, Iolascon A, Capasso M. Andolfo I, et al. Among authors: iolascon a. iScience. 2021 Apr 23;24(4):102322. doi: 10.1016/j.isci.2021.102322. Epub 2021 Mar 17. iScience. 2021. PMID: 33748697 Free PMC article.
Recommendations for diagnosis and treatment of methemoglobinemia.
Iolascon A, Bianchi P, Andolfo I, Russo R, Barcellini W, Fermo E, Toldi G, Ghirardello S, Rees D, Van Wijk R, Kattamis A, Gallagher PG, Roy N, Taher A, Mohty R, Kulozik A, De Franceschi L, Gambale A, De Montalembert M, Forni GL, Harteveld CL, Prchal J; SWG of red cell and iron of EHA and EuroBloodNet. Iolascon A, et al. Am J Hematol. 2021 Dec 1;96(12):1666-1678. doi: 10.1002/ajh.26340. Epub 2021 Sep 23. Am J Hematol. 2021. PMID: 34467556 Review.
Inherited microcytic anemias.
Cappellini MD, Russo R, Andolfo I, Iolascon A. Cappellini MD, et al. Among authors: iolascon a. Hematology Am Soc Hematol Educ Program. 2020 Dec 4;2020(1):465-470. doi: 10.1182/hematology.2020000158. Hematology Am Soc Hematol Educ Program. 2020. PMID: 33275715 Free PMC article. Review.
372 results