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Page 1
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. Among authors: mendez m. Eur J Haematol. 2018 Sep;101(3):368-378. doi: 10.1111/ejh.13112. Epub 2018 Jul 27. Eur J Haematol. 2018. PMID: 29901818
A case of congenital dyserythropoietic anemia type IV.
de-la-Iglesia-Iñigo S, Moreno-Carralero MI, Lemes-Castellano A, Molero-Labarta T, Méndez M, Morán-Jiménez MJ. de-la-Iglesia-Iñigo S, et al. Among authors: mendez m. Clin Case Rep. 2017 Jan 28;5(3):248-252. doi: 10.1002/ccr3.825. eCollection 2017 Mar. Clin Case Rep. 2017. PMID: 28265383 Free PMC article.
Sideroblastic anemia: functional study of two novel missense mutations in ALAS2.
Méndez M, Moreno-Carralero MI, Morado-Arias M, Fernández-Jiménez MC, de la Iglesia Iñigo S, Morán-Jiménez MJ. Méndez M, et al. Mol Genet Genomic Med. 2016 Jan 13;4(3):273-82. doi: 10.1002/mgg3.202. eCollection 2016 May. Mol Genet Genomic Med. 2016. PMID: 27247955 Free PMC article.
Missense variants in ALAS2 gene in five patients.
Moreno-Carralero MI, Arrizabalaga-Amuchastegui B, Sánchez-Calero-Guilarte J, Morado-Arias M, Velasco-Valdazo AE, de-la-Iglesia-Iñigo S, Méndez M, Morán-Jiménez MJ. Moreno-Carralero MI, et al. Among authors: mendez m. Int J Lab Hematol. 2019 Feb;41(1):e5-e9. doi: 10.1111/ijlh.12902. Epub 2018 Jul 17. Int J Lab Hematol. 2019. PMID: 30019527 No abstract available.
Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene.
Moreno-Risco MB, Méndez M, Moreno-Carralero MI, López-Moreno AM, Vagace-Valero JM, Morán-Jiménez MJ. Moreno-Risco MB, et al. Among authors: mendez m. Case Rep Pediatr. 2022 Apr 11;2022:7743748. doi: 10.1155/2022/7743748. eCollection 2022. Case Rep Pediatr. 2022. PMID: 35449524 Free PMC article.
The hereditary hyperferritinemia-cataract syndrome: a family study.
Álvarez-Coca-González J, Moreno-Carralero MI, Martínez-Pérez J, Méndez M, García-Ros M, Morán-Jiménez MJ. Álvarez-Coca-González J, et al. Among authors: mendez m. Eur J Pediatr. 2010 Dec;169(12):1553-5. doi: 10.1007/s00431-010-1251-2. Epub 2010 Jul 9. Eur J Pediatr. 2010. PMID: 20617342
A novel mutation in the SLC40A1 gene associated with reduced iron export in vitro.
Moreno-Carralero MI, Muñoz-Muñoz JA, Cuadrado-Grande N, López-Rodríguez R, José Hernández-Alfaro M, del-Castillo-Rueda A, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ. Moreno-Carralero MI, et al. Among authors: mendez m. Am J Hematol. 2014 Jul;89(7):689-94. doi: 10.1002/ajh.23714. Epub 2014 Apr 10. Am J Hematol. 2014. PMID: 24644245 Free article.
Molecular Analysis of 55 Spanish Patients with Acute Intermittent Porphyria.
Morán-Jiménez MJ, Borrero-Corte MJ, Jara-Rubio F, García-Pastor I, Díaz-Díaz S, Castelbón-Fernandez FJ, Enríquez-de-Salamanca R, Méndez M. Morán-Jiménez MJ, et al. Among authors: mendez m. Genes (Basel). 2020 Aug 12;11(8):924. doi: 10.3390/genes11080924. Genes (Basel). 2020. PMID: 32806544 Free PMC article.
Hepcidin treatment in Hfe-/- mice diminishes plasma iron without affecting erythropoiesis.
Morán-Jiménez MJ, Méndez M, Santiago B, Rodríguez-García ME, Moreno-Carralero MI, Sánchez-Lucío AC, Grau M, Enríquez-de-Salamanca R. Morán-Jiménez MJ, et al. Among authors: mendez m. Eur J Clin Invest. 2010 Jun;40(6):511-7. doi: 10.1111/j.1365-2362.2010.02291.x. Epub 2010 Apr 26. Eur J Clin Invest. 2010. PMID: 20456487
1,805 results