Detalhe da pesquisa
1.
Type 2N VWD: Conclusions from the Spanish PCM-EVW-ES project.
Haemophilia
; 27(6): 1007-1021, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34494337
2.
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study.
Haematologica
; 105(7): 1948-1956, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31558677
3.
Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management.
J Thromb Thrombolysis
; 50(3): 686-688, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32060721
4.
Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA.
Haematologica
; 104(3): 587-598, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30361419
5.
Novel mutations in RASGRP2, which encodes CalDAG-GEFI, abrogate Rap1 activation, causing platelet dysfunction.
Blood
; 128(9): 1282-9, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27235135
6.
Bleeding risk of surgery and its prevention in patients with inherited platelet disorders.
Haematologica
; 102(7): 1192-1203, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28385783
7.
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients.
Haematologica
; 102(12): 2005-2014, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28971901
8.
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.
Haemophilia
; 25(2): e97-e100, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30604912
9.
Cross-sectional comparative study of pharmacokinetics and efficacy between sucrose-formulated recombinant factor VIII (Kogenate® ) and BAY 81-8973 (Kovaltry® ) in patients with severe or moderate haemophilia A in prophylaxis.
Haemophilia
; 25(3): e215-e218, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30866068
10.
Challenges, questions and opportunities with regard to the new relationship between clinical practice and the haemostasis laboratory: the path towards personalized medicine.
Blood Coagul Fibrinolysis
; 2021 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34693914
11.
Clinical benefits of a Bayesian model for plasma-derived factor VIII/VWF after one year of pharmacokinetic-guided prophylaxis in severe/moderate hemophilia A patients.
Thromb Res
; 205: 99-105, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34293540
12.
The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology.
J Thromb Haemost
; 19(5): 1364-1371, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33880867
13.
Body Mass Index Best Predicts Recovery of Recombinant Factor VIII in Underweight to Obese Patients with Severe Haemophilia A.
Thromb Haemost
; 120(2): 277-288, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31887776
14.
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC.
J Thromb Haemost
; 18(3): 732-739, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31750621
15.
Unraveling the Influence of Common von Willebrand factor variants on von Willebrand Disease Phenotype: An Exploratory Study on the Molecular and Clinical Profile of von Willebrand Disease in Spain Cohort.
Thromb Haemost
; 120(3): 437-448, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32135566
16.
Novel missense mutation c.2685G>C (p.Q895H) in VWF gene associated with very low levels of VWF mRNA.
Ann Hematol
; 88(3): 245-7, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18712522
17.
Severe and moderate hemophilia A: identification of 38 new genetic alterations.
Haematologica
; 93(7): 1091-4, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18403393
18.
α2-Macroglobulin Is a Significant In Vivo Inhibitor of Activated Protein C and Low APC:α2M Levels Are Associated with Venous Thromboembolism.
Thromb Haemost
; 118(4): 630-638, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29448296
19.
Role of multimeric analysis of von Willebrand factor (VWF) in von Willebrand disease (VWD) diagnosis: Lessons from the PCM-EVW-ES Spanish project.
PLoS One
; 13(6): e0197876, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29924855
20.
Risk Factors for the Progression from Low to High Titres in 260 Children with Severe Haemophilia A and Newly Developed Inhibitors.
Thromb Haemost
; 117(12): 2274-2282, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29212115