Search Results - "Vázquez, Ramiro Núñez"
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Management of Urgent Bleeding in Patients with Hemophilia A: Focus on the Use of Emicizumab
Published in TH open : companion journal to thrombosis and haemostasis (01-04-2024)“…Management of patients with hemophilia A (HA) requires the knowledge and experience of specialized health care professionals. However, these patients may need…”
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Protocol for oral implant rehabilitation in a hemophilic HIV-positive patient with type C hepatitis
Published in Implant dentistry (01-10-2014)“…A 46-year-old man with severe hemophilia A, stage A2 HIV infection and chronic hepatitis C genotype 1A, for whom the treatment plan included implant-supported…”
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Avatrombopag plus fostamatinib combination as treatment in patients with multirefractory immune thrombocytopenia
Published in British journal of haematology (01-10-2024)“…Summary Immune thrombocytopenia (ITP) refractory to multiple therapies may require a combination of drugs targeting different mechanisms and targets. In this…”
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Acquired Haemophilia A: A Review of What We Know
Published in Journal of blood medicine (30-11-2022)“…Autoantibodies against plasma coagulation factors could be developed by some individuals inducing severe and sometimes fatal bleedings. This clinical entity is…”
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Treatment with fostamatinib in patients with immune thrombocytopenia: Experience from the Andalusian region in Spain—The Fostasur Study
Published in British journal of haematology (01-05-2024)“…Summary Immune thrombocytopenia (ITP) is characterized by low platelet counts (PLTs) and an increased risk of bleeding. Fostamatinib, a spleen tyrosine kinase…”
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Switching hemophilia A patients to rVIII-SingleChain: The Iberian experience
Published in Medicine (Baltimore) (06-09-2024)“…The real-world outcomes of lonoctocog alfa (rVIII-SingleChain), a long-acting factor VIII (FVIII) with a favorable safety and efficacy profile in trials, were…”
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Factor XIII Deficiency As Underlying Cause Of Unexplained Bleeding
Published in Blood (15-11-2013)“…Factor XIII deficiency (FXIII) is an uncommon coagulation disorder. Congenital FXIII deficiency, generally due to mutations in F13A1 gene, presents with early…”
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Consenso de recomendaciones para la mejora de la coordinación asistencial inter e intra-centros en el abordaje de la hemofilia
Published in Farmacia hospitalaria (01-05-2023)“…definir las recomendaciones consensuadas para mejorar la coordinación asistencial entre Farmacia Hospitalaria, Hematología y Enfermería, inter e intra-centros,…”
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Cathepsin K as a biomarker of bone involvement in type 1 Gaucher disease
Published in Medicina clínica (English ed.) (05-10-2015)“…Gaucher disease is an inherited disorder caused by deficit of acid β-glucocerebrosidase, responsible for the degradation of glucosylceramide to ceramide and…”
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2-years retrospective observational case-control study on survival and marginal bone loss of implants in patients with hereditary coagulopathies
Published in Medicina oral, patología oral y cirugía bucal (01-11-2023)“…Evaluating 2-years implant loss and marginal bone loss in patients with hereditary coagulopathies, comparing with a healthy control group. 37 implants in 13…”
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[Translated article] Consensus recommendations for the improvement of inter- and intra-centre care coordination in the management of hemophilia
Published in Farmacia hospitalaria (01-05-2023)“…Define consensus recommendations to improve care coordination between Hospital Pharmacy, Hematology and Nursing, inter- and intra-center, in the care of…”
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Platelet Responses After Tapering and Discontinuation of Fostamatinib in Patients with Immune Thrombocytopenia: A Continuation of the Fostasur Study
Published in Journal of clinical medicine (01-11-2024)“…Background/objectives: Fostamatinib is a spleen tyrosine kinase (SYK) inhibitor approved for the treatment of adult patients with chronic immune…”
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Humanistic burden of haemophilia A without inhibitors: A cross‐sectional analysis of the HemoLIFE study
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-07-2024)“…Aim To evaluate the impact of haemophilia A without inhibitors on humanistic outcomes in patients and caregivers. Herein, we report a cross‐sectional analysis…”
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Cathepsin K as a biomarker of bone involvement in type 1 Gaucher disease
Published in Medicina clinica (05-10-2015)“…Gaucher disease is an inherited disorder caused by deficit of acid β-glucocerebrosidase, responsible for the degradation of glucosylceramide to ceramide and…”
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[Translated article] Consensus recommendations for the improvement of inter- and intra-centre care coordination in the management of hemophilia
Published in Farmacia hospitalaria : organo oficial de expresion cientifica de la Sociedad Espanola de Farmacia Hospitalaria (01-05-2023)“…Define consensus recommendations to improve care coordination between Hospital Pharmacy, Hematology and Nursing, inter- and intra-center, in the care of…”
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Consensus recommendations for the improvement of inter- and intra-centre care coordination in the management of hemophilia
Published in Farmacia hospitalaria : organo oficial de expresion cientifica de la Sociedad Espanola de Farmacia Hospitalaria (01-05-2023)“…Define consensus recommendations to improve care coordination between Hospital Pharmacy, Haematology and Nursing, inter- and intra-center, in the care of…”
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The spectrum of mutations in Southern Spanish patients with hemophilia A and identification of 28 novel mutations
Published in Haematologica (Roma) (01-05-2005)“…The aim of this study was to analyze the mutation pattern causing hemophilia A in a population from Southern Spain. Mutation analysis identified the mutation…”
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