de la Fuente-Gonzalo F - Search Results

1

Phenotype of mutations in the promoter region of the β-globin gene.

Ropero P, Erquiaga S, Arrizabalaga B, Pérez G, de la Iglesia S, Torrejón MJ, Gil C, Elena C, Tenorio M, Nieto JM, de la Fuente-Gonzalo F, Villegas A, González Fernández FA, Martínez R. Ropero P, et al. Among authors: de la fuente gonzalo f. J Clin Pathol. 2017 Oct;70(10):874-878. doi: 10.1136/jclinpath-2017-204378. Epub 2017 Apr 6. J Clin Pathol. 2017. PMID: 28385923

2

Association in cis of the mutations +20 (C>T) in the 5' untranslated region and IVS-II-745 (C>G) on the β-globin gene.

Ropero P, González FA, Cela E, Beléndez C, Cervera A, Martínez-Nieto J, de la Fuente-Gonzalo F, Vinuesa L, Villegas A, Díaz-Mediavilla J. Ropero P, et al. Hemoglobin. 2013;37(2):112-8. doi: 10.3109/03630269.2013.766620. Epub 2013 Feb 21. Hemoglobin. 2013. PMID: 23425204

3

Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype.

Nieto JM, Villegas A, De La Fuente-Gonzalo F, González FA, Ropero P. Nieto JM, et al. J Hum Genet. 2014 Oct;59(10):585-7. doi: 10.1038/jhg.2014.76. Epub 2014 Sep 4. J Hum Genet. 2014. PMID: 25186056

4

Identification of a novel mutation in the β-globin gene 3' untranslated region (HBB: c.*+118A > G) in Spain.

Herrera MA, De La Fuente-Gonzalo F, González FA, Nieto JM, Dominguez AB, Villegas A, Ropero P. Herrera MA, et al. Hemoglobin. 2015;39(1):30-5. doi: 10.3109/03630269.2014.995805. Epub 2015 Jan 9. Hemoglobin. 2015. PMID: 25572186

5

[Delta⁰-thalassemia by insertion of 27 base pairs in δ-globin gene with decreased hemoglobin A₂ levels].

González Borrachero ML, de la Fuente-Gonzalo F, González FA, Nieto JM, Villegas A, Ropero P. González Borrachero ML, et al. Med Clin (Barc). 2015 Apr 8;144(7):312-6. doi: 10.1016/j.medcli.2014.10.021. Epub 2015 Jan 8. Med Clin (Barc). 2015. PMID: 25579773 Spanish.

6

Different forms of Hb Le Lamentin. An unexpected finding in Hba1c quantification.

Martínez-López R, de la Fuente-Gonzalo F, Nieto JM, Gallar CB, Román CR, Villegas A, González FA, Martínez R, Casado LN, Ropero P. Martínez-López R, et al. Among authors: de la fuente gonzalo f. Clin Biochem. 2016 Jan;49(1-2):57-60. doi: 10.1016/j.clinbiochem.2015.09.015. Epub 2015 Oct 5. Clin Biochem. 2016. PMID: 26436569

7

Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait.

Velasco-Rodríguez D, Alonso-Domínguez JM, González-Fernández FA, Muriel A, Abalo L, Sopeña M, Villarrubia J, Ropero P, Plaza MP, Tenorio M, Jiménez-Martín A, Moreno G, Martínez-Nieto J, de la Fuente-Gonzalo F, Fernández-Escribano M, López-Jiménez FJ, Cava F. Velasco-Rodríguez D, et al. Among authors: de la fuente gonzalo f. J Clin Pathol. 2016 Oct;69(10):912-20. doi: 10.1136/jclinpath-2015-203556. Epub 2016 Feb 25. J Clin Pathol. 2016. PMID: 26915371

8

Haemoglobinopathies that occur with decreased HbA2 levels: a gene mutation set involving the δ gene at a Spanish centre.

Villegas A, González FA, Nieto JM, de la Fuente-Gonzalo F, Martínez R, Torrejón MJ, Ropero P. Villegas A, et al. Among authors: de la fuente gonzalo f. J Clin Pathol. 2017 Jan;70(1):75-80. doi: 10.1136/jclinpath-2016-203879. Epub 2016 Jul 7. J Clin Pathol. 2017. PMID: 27387985

9

Characterization of deletional and non-deletional alpha globin variants in a large cohort from Spain between 2009 and 2014.

de la Fuente-Gonzalo F, Nieto JM, Villegas A, González FA, Martínez R, Ropero P. de la Fuente-Gonzalo F, et al. Ann Hematol. 2019 Jul;98(7):1537-1545. doi: 10.1007/s00277-019-03696-w. Epub 2019 Apr 25. Ann Hematol. 2019. PMID: 31025160

10

Hb Extremadura [β64(E8)Gly→Ser;β133(H11)Val→Leu]: a new molecular analysis.

Ropero P, Martín-Nuñez G, González FA, Villegas A, de la Fuente-Gonzalo F, Martínez-Nieto J, Vinuesa L, Díaz-Mediavilla J. Ropero P, et al. Hemoglobin. 2011;35(4):423-7. doi: 10.3109/03630269.2011.576353. Hemoglobin. 2011. PMID: 21797709

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