Vidal F - Search Results

1

Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing.

de la Morena-Barrio B, Palomo Á, Padilla J, Martín-Fernández L, Rojo-Carrillo JJ, Cifuentes R, Bravo-Pérez C, Garrido-Rodríguez P, Miñano A, Rubio AM, Pagán J, Llamas M, Vicente V, Vidal F, Lozano ML, Corral J, de la Morena-Barrio ME. de la Morena-Barrio B, et al. Among authors: vidal f. J Thromb Haemost. 2023 Jul;21(7):1779-1788. doi: 10.1016/j.jtha.2023.03.009. Epub 2023 Mar 20. J Thromb Haemost. 2023. PMID: 36940803

2

Rapid hemophilia A molecular diagnosis by a simple DNA sequencing procedure: identification of 14 novel mutations.

Vidal F, Farssac E, Altisent C, Puig L, Gallardo D. Vidal F, et al. Thromb Haemost. 2001 Apr;85(4):580-3. Thromb Haemost. 2001. PMID: 11341489

3

First molecular characterization of an unequal homologous alu-mediated recombination event responsible for hemophilia.

Vidal F, Farssac E, Tusell J, Puig L, Gallardo D. Vidal F, et al. Thromb Haemost. 2002 Jul;88(1):12-6. Thromb Haemost. 2002. PMID: 12154809

4

A versatile strategy for preimplantation genetic diagnosis of haemophilia A based on F8-gene sequencing.

Sánchez-García JF, Gallardo D, Navarro J, Márquez C, Gris JM, Sánchez MA, Altisent C, Vidal F. Sánchez-García JF, et al. Among authors: vidal f. Thromb Haemost. 2006 Dec;96(6):839-45. Thromb Haemost. 2006. PMID: 17139381

5

Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene.

Corrales I, Ramírez L, Altisent C, Parra R, Vidal F. Corrales I, et al. Among authors: vidal f. Thromb Haemost. 2009 Mar;101(3):570-6. doi: 10.1160/th08-08-0500. Thromb Haemost. 2009. PMID: 19277422

6

The study of the effect of splicing mutations in von Willebrand factor using RNA isolated from patients' platelets and leukocytes.

Corrales I, Ramírez L, Altisent C, Parra R, Vidal F. Corrales I, et al. Among authors: vidal f. J Thromb Haemost. 2011 Apr;9(4):679-88. doi: 10.1111/j.1538-7836.2011.04204.x. J Thromb Haemost. 2011. PMID: 21251206 Free article.

7

Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): Proposal for a new diagnostic paradigm.

Batlle J, Pérez-Rodríguez A, Corrales I, López-Fernández MF, Rodríguez-Trillo Á, Lourés E, Cid AR, Bonanad S, Cabrera N, Moret A, Parra R, Mingot-Castellano ME, Balda I, Altisent C, Pérez-Montes R, Fisac RM, Iruín G, Herrero S, Soto I, de Rueda B, Jiménez-Yuste V, Alonso N, Vilariño D, Arija O, Campos R, Paloma MJ, Bermejo N, Toll T, Mateo J, Arribalzaga K, Marco P, Palomo Á, Sarmiento L, Iñigo B, Nieto Mdel M, Vidal R, Martínez MP, Aguinaco R, César JM, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Cornudella R, Aguilar C, Borràs N, Vidal F. Batlle J, et al. Among authors: vidal r, vidal f. Thromb Haemost. 2016 Jan;115(1):40-50. doi: 10.1160/TH15-04-0282. Epub 2015 Aug 6. Thromb Haemost. 2016. PMID: 26245874

8

The Unravelling of the Genetic Architecture of Plasminogen Deficiency and its Relation to Thrombotic Disease.

Martin-Fernandez L, Marco P, Corrales I, Pérez R, Ramírez L, López S, Vidal F, Soria JM. Martin-Fernandez L, et al. Among authors: vidal f. Sci Rep. 2016 Dec 15;6:39255. doi: 10.1038/srep39255. Sci Rep. 2016. PMID: 27976734 Free PMC article.

9

Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis.

Martin-Fernandez L, Gavidia-Bovadilla G, Corrales I, Brunel H, Ramírez L, López S, Souto JC, Vidal F, Soria JM. Martin-Fernandez L, et al. Among authors: vidal f. PLoS One. 2017 Apr 26;12(4):e0176301. doi: 10.1371/journal.pone.0176301. eCollection 2017. PLoS One. 2017. PMID: 28445521 Free PMC article.

10

High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study.

Esteban J, de la Morena-Barrio ME, Salloum-Asfar S, Padilla J, Miñano A, Roldán V, Soria JM, Vidal F, Corral J, Vicente V. Esteban J, et al. Among authors: vidal f. Haemophilia. 2017 Nov;23(6):e488-e496. doi: 10.1111/hae.13356. Epub 2017 Sep 27. Haemophilia. 2017. PMID: 28960694

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