Haya S - Search Results

1

New mutations in exon 28 of the von Willebrand factor gene detected in patients with different types of von Willebrand's disease.

Casaña P, Martínez F, Haya S, Tavares A, Aznar JA. Casaña P, et al. Among authors: haya s. Haematologica. 2001 Apr;86(4):414-9. Haematologica. 2001. PMID: 11325649

2

Molecular analyses in hemophilia B families: identification of six new mutations in the factor IX gene.

Espinós C, Casaña P, Haya S, Cid AR, Aznar JA. Espinós C, et al. Among authors: haya s. Haematologica. 2003 Feb;88(2):235-6. Haematologica. 2003. PMID: 12604421 No abstract available.

3

Von Willebrand's disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency.

Casaña P, Cabrera N, Haya S, Cid AR, Aznar JA. Casaña P, et al. Among authors: haya s. Haematologica. 2006 Aug;91(8):1130-3. Epub 2006 Jul 25. Haematologica. 2006. PMID: 16870550

4

Severe and moderate hemophilia A: identification of 38 new genetic alterations.

Casaña P, Cabrera N, Cid AR, Haya S, Beneyto M, Espinós C, Cortina V, Dasí MA, Aznar JA. Casaña P, et al. Among authors: haya s. Haematologica. 2008 Jul;93(7):1091-4. doi: 10.3324/haematol.12344. Epub 2008 Apr 9. Haematologica. 2008. PMID: 18403393 Free article.

5

Search for mutations in a segment of the exon 28 of the human von Willebrand factor gene: new mutations, R1315C and R1341W, associated with type 2M and 2B variants.

Casaña P, Martínez F, Espinós C, Haya S, Lorenzo JI, Aznar JA. Casaña P, et al. Among authors: haya s. Am J Hematol. 1998 Sep;59(1):57-63. doi: 10.1002/(sici)1096-8652(199809)59:1<57::aid-ajh11>3.0.co;2-z. Am J Hematol. 1998. PMID: 9723578 Free article.

6

Identification of a new candidate mutation, G1629R, in a family with type 2A von Willebrand disease.

Casaña P, Martínez F, Haya S, Aznar JA. Casaña P, et al. Among authors: haya s. Am J Hematol. 1999 Apr;60(4):309-10. doi: 10.1002/(sici)1096-8652(199904)60:4<309::aid-ajh10>3.0.co;2-p. Am J Hematol. 1999. PMID: 10203106 Free article.

7

Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor gene.

Casaña P, Martínez F, Haya S, Lorenzo JI, Espinós C, Aznar JA. Casaña P, et al. Among authors: haya s. Br J Haematol. 2000 Nov;111(2):552-5. doi: 10.1046/j.1365-2141.2000.02410.x. Br J Haematol. 2000. PMID: 11122100 Free article.

8

Association of the 3467C>T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's disease.

Casaña P, Martínez F, Haya S, Espinós C, Aznar JA. Casaña P, et al. Among authors: haya s. Ann Hematol. 2001 Jul;80(7):381-3. doi: 10.1007/s002770100307. Ann Hematol. 2001. PMID: 11529461

9

Significant linkage and non-linkage of type 1 von Willebrand disease to the von Willebrand factor gene.

Casaña P, Martínez F, Haya S, Espinós C, Aznar JA. Casaña P, et al. Among authors: haya s. Br J Haematol. 2001 Dec;115(3):692-700. doi: 10.1046/j.1365-2141.2001.03132.x. Br J Haematol. 2001. PMID: 11736956 Free article.

10

Novel missense mutation c.2685G>C (p.Q895H) in VWF gene associated with very low levels of VWF mRNA.

Cabrera N, Casaña P, Cid AR, Haya S, Moret A, Aznar JA. Cabrera N, et al. Among authors: haya s. Ann Hematol. 2009 Mar;88(3):245-7. doi: 10.1007/s00277-008-0576-7. Epub 2008 Aug 20. Ann Hematol. 2009. PMID: 18712522

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