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

Year Number of Results
2002 2
2003 2
2004 4
2005 1
2007 6
2009 1
2010 3
2011 3
2012 4
2013 5
2014 2
2015 4
2016 4
2017 3
2018 2
2019 1
2020 3
2021 2
2022 5
2023 2
2024 1

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53 results

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Page 1
A newly identified ferritin L-subunit variant results in increased proteasomal subunit degradation, impaired complex assembly, and severe hypoferritinemia.
Shagidov D, Guttmann-Raviv N, Cunat S, Frech L, Giansily-Blaizot M, Ghatpande N, Abelya G, Frank GA, Aguilar Martinez P, Meyron-Holtz EG. Shagidov D, et al. Among authors: aguilar martinez p. Am J Hematol. 2024 Jan;99(1):12-20. doi: 10.1002/ajh.27124. Epub 2023 Oct 23. Am J Hematol. 2024. PMID: 37867341
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families.
Szepetowski S, Berger C, Joly P, Baron-Joly S, Huguenin Y, Cantais A, Brun S, Ged C, Badens C, Thuret I, Giansily-Blaizot M, Pissard S, Aguilar-Martinez P. Szepetowski S, et al. Among authors: aguilar martinez p. Am J Hematol. 2022 Nov;97(11):E393-E395. doi: 10.1002/ajh.26687. Epub 2022 Sep 2. Am J Hematol. 2022. PMID: 36052950 Free article. No abstract available.
A case of inter-assay HbA1c discrepancy due to Hemoglobin G-Copenhagen.
Badiou S, Dupuy AM, Cunat S, Delay A, Alcaraz S, Aguilar-Martinez P, Cristol JP, Galtier F. Badiou S, et al. Among authors: aguilar martinez p. Clin Chim Acta. 2022 Oct 1;535:27-29. doi: 10.1016/j.cca.2022.08.004. Epub 2022 Aug 10. Clin Chim Acta. 2022. PMID: 35963305
A simple clinical score to promote and enhance ferroportin disease screening.
Landemaine A, Hamdi-Roze H, Cunat S, Loustaud-Ratti V, Causse X, Si Ahmed SN, Drénou B, Bureau C, Pelletier G, De Kerguenec C, Ganne-Carrie N, Durupt S, Laine F, Loréal O, Ropert M, Detivaud L, Morcet J, Aguilar-Martinez P, Deugnier YM, Bardou-Jacquet E. Landemaine A, et al. Among authors: aguilar martinez p. J Hepatol. 2022 Mar;76(3):568-576. doi: 10.1016/j.jhep.2021.10.022. Epub 2021 Nov 5. J Hepatol. 2022. PMID: 34748893 Free article.
Increased incidence of germline PIEZO1 mutations in individuals with idiopathic erythrocytosis.
Filser M, Giansily-Blaizot M, Grenier M, Monedero Alonso D, Bouyer G, Pérès L, Egée S, Aral B, Airaud F, Da Costa L, Picard V, Cougoul P, Palach M, Béziau S, Garrec C, Aguilar-Martinez P, Gardie B, Girodon F. Filser M, et al. Among authors: aguilar martinez p. Blood. 2021 Apr 1;137(13):1828-1832. doi: 10.1182/blood.2020008424. Blood. 2021. PMID: 33181827 Free article. No abstract available.
Recommendations for Pregnancy in Rare Inherited Anemias.
Taher AT, Iolascon A, Matar CF, Bou-Fakhredin R, de Franceschi L, Cappellini MD, Barcellini W, Russo R, Andolfo I, Tyan P, Gulbis B, Aydinok Y, Anagnou NP, Bencaiova GA, Tamary H, Martinez PA, Forni G, Vindigni R. Taher AT, et al. Among authors: martinez pa. Hemasphere. 2020 Aug 12;4(4):e446. doi: 10.1097/HS9.0000000000000446. eCollection 2020 Aug. Hemasphere. 2020. PMID: 32885142 Free PMC article. Review.
53 results