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2002 2
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2007 5
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2013 4
2014 2
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2017 2
2018 2
2019 1
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Page 1
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia.
Iolascon A, Andolfo I, Russo R, Sanchez M, Busti F, Swinkels D, Aguilar Martinez P, Bou-Fakhredin R, Muckenthaler MU, Unal S, Porto G, Ganz T, Kattamis A, De Franceschi L, Cappellini MD, Munro MG, Taher A; from EHA‐SWG Red Cell and Iron. Iolascon A, et al. Among authors: aguilar martinez p. Hemasphere. 2024 Jul 15;8(7):e108. doi: 10.1002/hem3.108. eCollection 2024 Jul. Hemasphere. 2024. PMID: 39011129 Free PMC article.
Predictors of health-related quality of life in a large cohort of adult patients living with sickle cell disease in France: the DREPAtient study.
Yaya I, Pourageaud A, Derbez B, Odièvre MH, Oudin Doglioni D, Podevin M, Thomas G, Yombo-Kokule L, Godart C, Lepetit M, Cassubie-Mercier T, Galacteros F, Chassany O; DREPAtient study group. Yaya I, et al. Front Public Health. 2024 May 20;12:1374805. doi: 10.3389/fpubh.2024.1374805. eCollection 2024. Front Public Health. 2024. PMID: 38832226 Free PMC article.
Bleeding risk in hemophilia A and B carriers: comparison of factor levels determined using chronometric and chromogenic assays.
Chiffré-Rakotoarivony D, Diaz-Cau I, Ranc A, Champiat MA, Rousseau F, Gournay-Garcia C, Théron A, Navarro R, Boulot P, Aguilar-Martinez P, Sauguet P, Biron-Andréani C. Chiffré-Rakotoarivony D, et al. Among authors: aguilar martinez p. Blood Coagul Fibrinolysis. 2024 Jul 1;35(5):232-237. doi: 10.1097/MBC.0000000000001305. Epub 2024 Apr 26. Blood Coagul Fibrinolysis. 2024. PMID: 38700721
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 Free article.
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.
Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients.
Picard V, Guitton C, Thuret I, Rose C, Bendelac L, Ghazal K, Aguilar-Martinez P, Badens C, Barro C, Bénéteau C, Berger C, Cathébras P, Deconinck E, Delaunay J, Durand JM, Firah N, Galactéros F, Godeau B, Jaïs X, de Jaureguiberry JP, Le Stradic C, Lifermann F, Maffre R, Morin G, Perrin J, Proulle V, Ruivard M, Toutain F, Lahary A, Garçon L. Picard V, et al. Among authors: aguilar martinez p. Haematologica. 2019 Aug;104(8):1554-1564. doi: 10.3324/haematol.2018.205328. Epub 2019 Jan 17. Haematologica. 2019. PMID: 30655378 Free PMC article.
Hepcidin: immunoanalytic characteristics.
Wolff F, de Verneuil H, Rucheton B, Lefebvre T, Vialaret J, Ropert-Bouchet M, Cunat S, Aguilar-Martinez P, Lehmann S, Delaby C. Wolff F, et al. Among authors: aguilar martinez p. Ann Biol Clin (Paris). 2018 Dec 1;76(6):705-715. doi: 10.1684/abc.2018.1382. Ann Biol Clin (Paris). 2018. PMID: 30257815 Free article. Review. English.
Differing impact of the deletion of hemochromatosis-associated molecules HFE and transferrin receptor-2 on the iron phenotype of mice lacking bone morphogenetic protein 6 or hemojuvelin.
Latour C, Besson-Fournier C, Meynard D, Silvestri L, Gourbeyre O, Aguilar-Martinez P, Schmidt PJ, Fleming MD, Roth MP, Coppin H. Latour C, et al. Among authors: aguilar martinez p. Hepatology. 2016 Jan;63(1):126-37. doi: 10.1002/hep.28254. Epub 2015 Nov 12. Hepatology. 2016. PMID: 26406355
Haemoglobinopathies in Europe: health & migration policy perspectives.
Aguilar Martinez P, Angastiniotis M, Eleftheriou A, Gulbis B, Mañú Pereira Mdel M, Petrova-Benedict R, Corrons JL. Aguilar Martinez P, et al. Orphanet J Rare Dis. 2014 Jul 1;9:97. doi: 10.1186/1750-1172-9-97. Orphanet J Rare Dis. 2014. PMID: 24980780 Free PMC article.
Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations.
Bardou-Jacquet E, Cunat S, Beaumont-Epinette MP, Kannengiesser C, Causse X, Sauvion S, Pouliquen B, Deugnier Y, David V, Loréal O, Aguilar-Martinez P, Brissot P, Jouanolle AM. Bardou-Jacquet E, et al. Among authors: aguilar martinez p. Br J Haematol. 2013 Jul;162(2):278-81. doi: 10.1111/bjh.12350. Epub 2013 Apr 18. Br J Haematol. 2013. PMID: 23600741 Free article. No abstract available.
Porphyria cutanea tarda and spherocytosis: a non-random association?
Du-Thanh A, Aguilar-Martinez P, Enescu C, Cunat S, Guillot B, Dereure O. Du-Thanh A, et al. Among authors: aguilar martinez p. Acta Derm Venereol. 2013 May;93(3):377-8. doi: 10.2340/00015555-1493. Acta Derm Venereol. 2013. PMID: 23093332 Free article. No abstract available.
Inactive matriptase-2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activity.
Guillem F, Kannengiesser C, Oudin C, Lenoir A, Matak P, Donadieu J, Isidor B, Méchinaud F, Aguilar-Martinez P, Beaumont C, Vaulont S, Grandchamp B, Nicolas G. Guillem F, et al. Among authors: aguilar martinez p. Hum Mutat. 2012 Sep;33(9):1388-96. doi: 10.1002/humu.22116. Epub 2012 May 30. Hum Mutat. 2012. PMID: 22581667 Free article.
Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome.
Flatt JF, Guizouarn H, Burton NM, Borgese F, Tomlinson RJ, Forsyth RJ, Baldwin SA, Levinson BE, Quittet P, Aguilar-Martinez P, Delaunay J, Stewart GW, Bruce LJ. Flatt JF, et al. Among authors: aguilar martinez p. Blood. 2011 Nov 10;118(19):5267-77. doi: 10.1182/blood-2010-12-326645. Epub 2011 Jul 26. Blood. 2011. PMID: 21791420 Free article.
[Flowcharts for the diagnosis and the molecular characterization of hemoglobinopathies].
Aguilar-Martinez P, Badens C, Bonello-Palot N, Cadet E, Couque N, Ducrocq R, Elion J, Francina A, Joly P, Pissard S, Rochette J; Réseay DHOS Pathologie héréditaire de l'érythrocyte. Aguilar-Martinez P, et al. Ann Biol Clin (Paris). 2010 Jul-Aug;68(4):455-64. doi: 10.1684/abc.2010.0457. Ann Biol Clin (Paris). 2010. PMID: 20650741 Free article. French.
The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance.
Aguilar-Martinez P, Bismuth M, Blanc F, Blanc P, Cunat S, Dereure O, Dujols P, Giansily-Blaizot M, Jorgensen C, Konate A, Larrey D, Le Quellec A, Mura T, Raingeard I, Ramos J, Renard E, Rousseau F, Schved JF, Picot MC. Aguilar-Martinez P, et al. Haematologica. 2010 Apr;95(4):551-6. doi: 10.3324/haematol.2009.014431. Epub 2010 Feb 9. Haematologica. 2010. PMID: 20145272 Free PMC article.
Global sequencing approach for characterizing the molecular background of hereditary iron disorders.
Cunat S, Giansily-Blaizot M, Bismuth M, Blanc F, Dereure O, Larrey D, Quellec AL, Pouderoux P, Rose C, Raingeard I, Renard E, Schved JF, Aguilar-Martinez P; CHU Montpellier AOI 2004 Working Group. Cunat S, et al. Among authors: aguilar martinez p. Clin Chem. 2007 Dec;53(12):2060-9. doi: 10.1373/clinchem.2007.090605. Epub 2007 Oct 19. Clin Chem. 2007. PMID: 17951290
[Non-HFE-related hereditary iron overload].
Aguilar-Martinez P. Aguilar-Martinez P. Presse Med. 2007 Sep;36(9 Pt 2):1279-91. doi: 10.1016/j.lpm.2007.01.042. Epub 2007 May 30. Presse Med. 2007. PMID: 17540536 Review. French.
Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction.
Fricke B, Jarvis HG, Reid CD, Aguilar-Martinez P, Robert A, Quittet P, Chetty M, Pizzey A, Cynober T, Lande WF, Mentzer WC, Düring M, Winter S, Delaunay J, Stewart GW. Fricke B, et al. Among authors: aguilar martinez p. Br J Haematol. 2004 Jun;125(6):796-803. doi: 10.1111/j.1365-2141.2004.04965.x. Br J Haematol. 2004. PMID: 15180870 Free article.
[Hereditary haemochromatosis].
Bismuth M, Aguilar-Martinez P, Michel H. Bismuth M, et al. Among authors: aguilar martinez p. Presse Med. 2003 Nov 8;32(36):1716-23. Presse Med. 2003. PMID: 14663401 Review. French.
Two novel cases of cerebral haemorrhages at the neonatal period associated with inherited factor VII deficiency, one of them revealing a new nonsense mutation (Ser52Stop).
Giansily-Blaizot M, Aguilar-Martinez P, Briquel ME, d'Oiron R, De Maistre E, Epelbaum S, Schved JF. Giansily-Blaizot M, et al. Among authors: aguilar martinez p. Blood Coagul Fibrinolysis. 2003 Feb;14(2):217-20. doi: 10.1097/00001721-200302000-00016. Blood Coagul Fibrinolysis. 2003. PMID: 12632035 Review.
Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding.
Giansily-Blaizot M, Biron-Andreani C, Aguilar-Martinez P, de Moeloose P, Briquel ME, Goudemand J, Stieltjes N, Barrot C, Chambost H, Durin A, Gay V, Peynet J, Pouymayou K, Schved JF. Giansily-Blaizot M, et al. Among authors: aguilar martinez p. Br J Haematol. 2002 Apr;117(1):172-5. doi: 10.1046/j.1365-2141.2002.03408.x. Br J Haematol. 2002. PMID: 11918551 Free article.