Baena M - Search Results

1

Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis.

Tizzano E, Venceslá A, Cornet M, Baena M, Baiget M. Tizzano E, et al. Among authors: baena m. Haemophilia. 2005 Mar;11(2):142-4. doi: 10.1111/j.1365-2516.2005.01071.x. Haemophilia. 2005. PMID: 15810916

2

Rapid identification of female haemophilia A carriers with deletions in the factor VIII gene by quantitative real-time PCR analysis.

Tizzano EF, Barceló MJ, Baena M, Cornet M, Venceslá A, Mateo J, Fontcuberta J, Baiget M. Tizzano EF, et al. Among authors: baena m. Thromb Haemost. 2005 Sep;94(3):661-4. doi: 10.1160/TH05-03-0144. Thromb Haemost. 2005. PMID: 16268486

3

First report of two independent point factorVIII mutations in a family with haemophilia a: a word of caution for carrier diagnosis.

Tizzano EF, Venceslá A, Baena M, Cornet M, Calvo MT, Lucía JF, Pérez Garrido R, Núñez R, Baiget M. Tizzano EF, et al. Among authors: baena m. Thromb Haemost. 2005 Sep;94(3):675-7. doi: 10.1160/TH05-03-0675. Thromb Haemost. 2005. PMID: 16268489 No abstract available.

4

Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A.

Venceslá A, Baena M, Fares Taie L, Cornet M, Baiget M, Tizzano EF. Venceslá A, et al. Among authors: baena m. Haemophilia. 2008 May;14(3):489-93. doi: 10.1111/j.1365-2516.2008.01698.x. Epub 2008 Apr 1. Haemophilia. 2008. PMID: 18384354

5

Severe haemophilia A in a female resulting from an inherited gross deletion and a de novo codon deletion in the F8 gene.

Venceslá A, Fuentes-Prior P, Baena M, Quintana M, Baiget M, Tizzano EF. Venceslá A, et al. Among authors: baena m. Haemophilia. 2008 Sep;14(5):1094-8. doi: 10.1111/j.1365-2516.2008.01816.x. Epub 2008 Jul 25. Haemophilia. 2008. PMID: 18665854 Review.

6

F8 gene dosage defects in atypical patients with severe haemophilia A.

Venceslá Á, Baena M, Garrido RP, Núñez R, Velasco F, Rosell J, Villar A, Jiménez-Yuste V, Baiget M, Tizzano EF. Venceslá Á, et al. Among authors: baena m. Haemophilia. 2012 Sep;18(5):708-13. doi: 10.1111/j.1365-2516.2012.02818.x. Epub 2012 May 23. Haemophilia. 2012. PMID: 22621702

7

Marker and real-time quantitative analyses to confirm hemophilia B carrier diagnosis of a complete deletion of the F9 gene.

Venceslá A, Barceló MJ, Baena M, Quintana M, Baiget M, Tizzano EF. Venceslá A, et al. Among authors: baena m. Haematologica. 2007 Nov;92(11):1583-4. doi: 10.3324/haematol.10693. Haematologica. 2007. PMID: 18024414 Free article.

8

Identification of 31 novel mutations in the F8 gene in Spanish hemophilia A patients: structural analysis of 20 missense mutations suggests new intermolecular binding sites.

Venceslá A, Corral-Rodríguez MA, Baena M, Cornet M, Domènech M, Baiget M, Fuentes-Prior P, Tizzano EF. Venceslá A, et al. Among authors: baena m. Blood. 2008 Apr 1;111(7):3468-78. doi: 10.1182/blood-2007-08-108068. Epub 2008 Jan 9. Blood. 2008. PMID: 18184865 Free PMC article.

9

Mutations in the NKX2-5 gene in patients with stroke and patent foramen ovale.

Belvís R, Tizzano EF, Martí-Fàbregas J, Leta RG, Baena M, Carreras F, Pons-Lladó G, Baiget M, Martí-Vilalta JL. Belvís R, et al. Among authors: baena m. Clin Neurol Neurosurg. 2009 Sep;111(7):574-8. doi: 10.1016/j.clineuro.2009.04.004. Epub 2009 May 21. Clin Neurol Neurosurg. 2009. PMID: 19464101

10

Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser.

Martín-Salces M, Venceslá A, Alvárez-Román MT, Rivas I, Fernandez I, Butta N, Baena M, Fuentes-Prior P, Tizzano EF, Jiménez-Yuste V. Martín-Salces M, et al. Among authors: baena m. Thromb Haemost. 2010 Oct;104(4):718-23. doi: 10.1160/TH10-02-0085. Epub 2010 Jul 20. Thromb Haemost. 2010. PMID: 20664893

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