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

Year Number of Results
2002 1
2004 3
2005 1
2007 1
2014 1
2016 1
2017 1
2018 3
2019 2
2020 2
2021 2
2022 1
2024 0

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16 results

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Page 1
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: moran jimenez mj. Case Rep Pediatr. 2022 Apr 11;2022:7743748. doi: 10.1155/2022/7743748. eCollection 2022. Case Rep Pediatr. 2022. PMID: 35449524 Free PMC article.
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: moran jimenez mj. Eur J Haematol. 2018 Sep;101(3):368-378. doi: 10.1111/ejh.13112. Epub 2018 Jul 27. Eur J Haematol. 2018. PMID: 29901818
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. Genes (Basel). 2020 Aug 12;11(8):924. doi: 10.3390/genes11080924. Genes (Basel). 2020. PMID: 32806544 Free PMC article.
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: moran jimenez mj. 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.
Molecular analysis of 19 Spanish patients with mixed porphyrias.
Borrero Corte MJ, Jara Rubio F, Morán Jiménez MJ, Díaz Díaz S, Castelbón Fernandez FJ, García Pastor I, Enríquez de Salamanca R, Méndez M. Borrero Corte MJ, et al. Among authors: moran jimenez mj. Eur J Med Genet. 2019 Dec;62(12):103589. doi: 10.1016/j.ejmg.2018.11.023. Epub 2018 Nov 23. Eur J Med Genet. 2019. PMID: 30476629
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: moran jimenez mj. 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.
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. Among authors: moran jimenez mj. Ann Hematol. 2021 Feb;100(2):353-364. doi: 10.1007/s00277-020-04319-5. Epub 2020 Nov 7. Ann Hematol. 2021. PMID: 33159567
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. Among authors: moran jimenez mj. 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.
16 results