Search Results - "Bonanad, S"

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    Haemophilic arthropathy: basic protocols for clinical examination and imaging by Querol, F., Querol-Giner, F., Aguilar, M., Bonanad, S., Marqués, E., Blasco, JM, Pérez-Alenda, S.

    Published in Blood coagulation & fibrinolysis (01-06-2023)
    “…In haemophilia, screening protocols in the prevention and treatment of common lesions still require unification of criteria. Patients with haemophilia seek…”
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    Journal Article
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    Bayesian pharmacokinetic-guided prophylaxis with recombinant factor VIII in severe or moderate haemophilia A by Megías-Vericat, J.E., Bonanad, S., Haya, S., Cid, A.R., Marqués, M.R., Monte, E., Pérez-Alenda, S., Bosch, P., Querol, F., Poveda, J.L.

    Published in Thrombosis research (01-02-2019)
    “…Personalised pharmacokinetics (PK) using Bayesian analysis with limited sampling is assumed to help to optimise prophylaxis in haemophilia A (HA) patients. Our…”
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    Journal Article
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    Novel investigations on the protective role of the FVIII/VWF complex in inhibitor development by Mannucci, P. M., Shi, Q., Bonanad, S., Klamroth, R.

    “…Summary Development of inhibitory antibodies to infused factor VIII (FVIII) concentrates is the most serious unresolved complication of haemophilia A…”
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    Journal Article
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    HaemoPREF: Further evaluation of patient perception and preference for treatment in a real world setting by Bonanad, S., Schulz, M., Gordo, A., Spurden, D., Cicchetti, M., Cappelleri, J. C., Tolley, C., Staunton, H., Brohan, E.

    “…Introduction Adherence to haemophilia A (HA) treatment may be influenced by patients’ beliefs about their condition and treatment. Furthermore, difficulties…”
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    Journal Article
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    Next generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiency by Moret, A., Zúñiga, Ángel, Ibáñez, M., Cid, A. R., Haya, S., Ferrando, F., Blanquer, A., Cervera, J., Bonanad, S.

    Published in Journal of thrombosis and thrombolysis (01-11-2019)
    “…Inherited bleeding coagulation disorders (IBCDs) have a powerful diagnostic tool in next generation sequencing (NGS) that not only offers confirmation of…”
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    Journal Article
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    Effect of radiosynoviorthesis on the progression of arthropathy and haemarthrosis reduction in haemophilic patients by Querol‐Giner, M., Pérez‐Alenda, S., Aguilar‐Rodríguez, M., Carrasco, J. J., Bonanad, S., Querol, F.

    “…Introduction Repeated haemarthrosis is widely accepted as the triggering cause of synovitis and haemophilic arthropathy. A first‐line treatment of chronic…”
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    Pilot evaluation of home delivery programme in haemophilia by Megías‐Vericat, J. E., Monte‐Boquet, E., Martín‐Cerezuela, M., Cuéllar‐Monreal, M. J., Tarazona‐Casany, M. V., Pérez‐Huertas, P., Bonanad, S., Poveda‐Andrés, J. L.

    “…Summary What is known and objectives Most of the clotting factor (CF) dispensations to haemophiliac patients are centralized in a few haemophilia treatment…”
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    Journal Article
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    Inhibitor development after switching of FVIII concentrate in multitransfused patients with severe haemophilia A by Aznar, J. A., Moret, A., Ibáñez, F., Vila, C., Cabrera, N., Mesa, E., Bonanad, S.

    “…Summary Switching between different therapeutic FVIII concentrate types has been postulated as a possible cause of inhibitor development in patient with…”
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    Journal Article
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