María Fernanda
López Fernández
Universidade da Coruña
La Coruña, EspañaPublicacións en colaboración con investigadores/as de Universidade da Coruña (14)
2021
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A decade of changes in management of immune thrombocytopenia, with special focus on elderly patients
Blood Cells, Molecules, and Diseases, Vol. 86
2020
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Oral Anticoagulation and Risk of Symptomatic Hemorrhagic Transformation in Stroke Patients Treated With Mechanical Thrombectomy: Data From the Nordictus Registry
Frontiers in Neurology, Vol. 11
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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
Thrombosis and Haemostasis, Vol. 120, Núm. 3, pp. 437-448
2019
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Deciphering predictive factors for choice of thrombopoietin receptor agonist, treatment free responses, and thrombotic events in immune thrombocytopenia
Scientific Reports, Vol. 9, Núm. 1
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Identification of 58 mutations (26 Novel) in 94 of 109 symptomatic Spanish probands with protein C deficiency
Thrombosis and Haemostasis, Vol. 119, Núm. 9, pp. 1409-1418
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Involvement of antifactor VIII autoantibodies specificity in the outcome of inhibitor eradication therapies in acquired hemophilia a patients
Blood Coagulation and Fibrinolysis, Vol. 30, Núm. 3, pp. 127-132
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Management of adult patients with primary immune thrombocytopenia (itp) in clinical practice: A consensus approach of the Spanish itp expert group
Advances in Hematology, Vol. 2019
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Update on Molecular Testing in von Willebrand Disease
Seminars in Thrombosis and Hemostasis, Vol. 45, Núm. 7, pp. 708-719
2018
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Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
Haematologica, Vol. 103, Núm. 1, pp. 148-162
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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, Vol. 13, Núm. 6
2016
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Molecular and clinical profile of von willebrand disease in spain (PCM-EVW-ES): Proposal for a new diagnostic paradigm
Thrombosis and Haemostasis, Vol. 115, Núm. 1, pp. 40-50
2014
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A novel mutation in adamts13 of a child with upshaw-schulman syndrome
Thrombosis and Haemostasis
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Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): A short review
Thrombosis Research, Vol. 134, Núm. 6, pp. 1171-1175
2011
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Acquired von Willebrand syndrome and mitral valve prosthesis leakage. A pilot study
European Journal of Haematology, Vol. 87, Núm. 5, pp. 448-456