Casaña P - Search Results

Year	Number of Results
1989	3
1995	3
1996	1
1998	1
1999	1
2000	3
2001	6
2002	1
2003	1
2005	1
2006	1
2007	3
2008	4
2009	2
2010	1
2011	1
2012	1
2015	1
2016	1
2019	1
2024	0

1

Inhibitors in haemophilia A: current management and open issues.

Haya S, Moret A, Cid AR, Cortina V, Casaña P, Cabrera N, Aznar JA. Haya S, et al. Among authors: casana p. Haemophilia. 2007 Dec;13 Suppl 5:52-60. doi: 10.1111/j.1365-2516.2007.01574.x. Haemophilia. 2007. PMID: 18078398 Review.

2

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: casana p. Ann Hematol. 2009 Mar;88(3):245-7. doi: 10.1007/s00277-008-0576-7. Epub 2008 Aug 20. Ann Hematol. 2009. PMID: 18712522

3

The incidence and treatment of bleeding episodes in non-severe haemophilia A patients with inhibitors.

van Velzen AS, Eckhardt CL, Streefkerk N, Peters M, Hart DP, Hamulyak K, Klamroth R, Meijer K, Nijziel M, Schinco P, Yee TT, van der Bom JG, Fijnvandraat K; INSIGHT study group. van Velzen AS, et al. Thromb Haemost. 2016 Mar;115(3):543-50. doi: 10.1160/TH15-03-0212. Epub 2015 Nov 19. Thromb Haemost. 2016. PMID: 26582077

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. Haematologica. 2008 Jul;93(7):1091-4. doi: 10.3324/haematol.12344. Epub 2008 Apr 9. Haematologica. 2008. PMID: 18403393 Free article.

5

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. 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.

6

Predictive factors of immune tolerance treatment response in severe haemophilia A patients with inhibitors: A real-world report from a single centre, mixed retrospective-prospective long-term study.

Haya S, Solano C, Cid AR, Argilés B, Hervás D, Querol F, Bonanad S, Casaña P. Haya S, et al. Among authors: casana p. Haemophilia. 2019 Mar;25(2):e97-e100. doi: 10.1111/hae.13660. Epub 2019 Jan 3. Haemophilia. 2019. PMID: 30604912 Free PMC article. No abstract available.

7

[Arrhythmogenic implications of non-iatrogenic thyroid dysfunction].

Inama G, Furlanello F, Fiorentini F, Braito G, Vergara G, Casana P. Inama G, et al. Among authors: casana p. G Ital Cardiol. 1989 Apr;19(4):303-10. G Ital Cardiol. 1989. PMID: 2753273 Italian.

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. Ann Hematol. 2001 Jul;80(7):381-3. doi: 10.1007/s002770100307. Ann Hematol. 2001. PMID: 11529461

9

A comparison of FVII:C and FVIIa assays for the monitoring of recombinant factor VIIa treatment.

Cid AR, Lorenzo JI, Haya S, Montoro JM, Casaña P, Aznar JA. Cid AR, et al. Among authors: casana p. Haemophilia. 2001 Jan;7(1):39-41. doi: 10.1046/j.1365-2516.2001.00478.x. Haemophilia. 2001. PMID: 11136379

10

Identification of deletion carriers in hemophilia B: quantitative real-time polymerase chain reaction or multiple ligation probe amplification.

Casaña P, Haya S, Cid AR, Oltra S, Martínez F, Cabrera N, Aznar JA. Casaña P, et al. Transl Res. 2009 Mar;153(3):114-7. doi: 10.1016/j.trsl.2008.12.006. Epub 2009 Jan 27. Transl Res. 2009. PMID: 19218093

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