Ropero P - Search Results

1

Study of three families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish population: three homozygous cases.

de la Fuente-Gonzalo F, Baiget M, Badell I, Ricard P, Vinuesa L, Martínez-Nieto J, Ropero P, Villegas A, González FA, Díaz-Mediavilla J, Erythropathology Spanish Group. de la Fuente-Gonzalo F, et al. Among authors: ropero p. Hemoglobin. 2012;36(6):526-32. doi: 10.3109/03630269.2012.733988. Epub 2012 Oct 24. Hemoglobin. 2012. PMID: 23094635

2

Hb Clinico-Madrid II [alpha90(FG2)Lys-->Arg (alpha1)] and Hb El Escorial [alpha96(G3)Val-->Asp (alpha2)]: two new a chain variants found during a neonatal period study.

Villegas A, Hojas R, González FA, Ropero P, Carreño DL. Villegas A, et al. Among authors: ropero p. Hemoglobin. 2003 Aug;27(3):185-90. doi: 10.1081/hem-120023383. Hemoglobin. 2003. PMID: 12908804 No abstract available.

3

[Hemoglobin Korle-Bu [beta73(E17)Asp ->Asn]. First cases described in Spain].

Ropero P, Villegas A, González FA. Ropero P, et al. Med Clin (Barc). 2004 Sep 4;123(7):260-1. doi: 10.1016/s0025-7753(04)74482-6. Med Clin (Barc). 2004. PMID: 15482733 Spanish.

4

A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).

Martin G, Villegas A, González FA, Ropero P, Hojas R, Polo M, Mateo M, Salvador M, Benavente C. Martin G, et al. Among authors: ropero p. Hemoglobin. 2005;29(2):113-7. Hemoglobin. 2005. PMID: 15921163

5

The first case of Hb E-Saskatoon associated with Hb Lepore-Baltimore found in Spain.

Ropero P, Murga MJ, González FA, Polo M, Benavente C, Salvador M, Villegas A. Ropero P, et al. Hemoglobin. 2005;29(3):215-9. doi: 10.1081/hem-200066321. Hemoglobin. 2005. PMID: 16114185

6

First Spanish case of thalassemia major due to a compound heterozygosity for the IVS-II-848 (C --> A) and codon 39 (C --> T) mutations of the beta-globin gene.

Ropero P, Villegas A, Muñoz J, Briceño O, Mora A, Salvador M, Polo M, González FA. Ropero P, et al. Hemoglobin. 2006;30(1):15-21. doi: 10.1080/03630260500453875. Hemoglobin. 2006. PMID: 16540410

7

Hb La Coruña [beta38(C4)Thr-->Ile]: a new hemoglobin variant leading to familial polycythemia.

Ropero P, Fernández-Lago C, Villegas A, Polo M, Mateo M, Mora A, González FA. Ropero P, et al. Hemoglobin. 2006;30(3):379-83. doi: 10.1080/03630260600755666. Hemoglobin. 2006. PMID: 16840229

8

Origin of the frameshift codons 41/42 (-TCTT) mutation in the first cases described in the Spanish population.

Ropero P, de la Iglesia S, Calvo-Villas JM, González FA, Paúl R, Villegas A. Ropero P, et al. Hemoglobin. 2008;32(5):513-9. doi: 10.1080/03630260802341968. Hemoglobin. 2008. PMID: 18932079

9

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

10

Erythrocytosis in a child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] associated with a Spanish (δβ)(0)-thalassemia.

Ropero P, González FA, Cela E, Beléndez C, Pérez B, Seri C, Fontanes E, Villegas A, Díaz-Mediavilla J. Ropero P, et al. Hemoglobin. 2013;37(1):48-55. doi: 10.3109/03630269.2012.746943. Epub 2012 Dec 10. Hemoglobin. 2013. PMID: 23215953

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