Atención Primaria A Coruña
Centro asistencial
Publicacións nas que colabora con María Fernanda López Fernández (12)
2019
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Unraveling the effect of silent, intronic and missense mutations on VWF splicing: Contribution of next generation sequencing in the study of mRNA
Haematologica, Vol. 104, Núm. 3, pp. 587-598
2018
2017
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Molecular and clinical profile of von willebrand disease in Spain (PCM-EVW-ES): Comprehensive genetic analysis by next-generation sequencing of 480 patients
Haematologica, Vol. 102, Núm. 12, pp. 2005-2014
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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Diagnosis of inherited von Willebrand disease: Comparison of two methodologies and analysis of the discrepancies
Haemophilia, Vol. 20, Núm. 4, pp. 559-567
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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
2009
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Autosomal dominant C1149R von Willebrand disease: Phenotypic findings and their implications
Haematologica, Vol. 94, Núm. 5, pp. 679-686
2005
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Von Willebrand disease R1374C: Type 2A or 2M? A challenge to the revised classification. High frequency in the northwest of Spain (Galicia)
American Journal of Hematology, Vol. 80, Núm. 3, pp. 188-196
1997
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Alloantibody from a patient with severe von Willebrand disease inhibits von Willebrand factor-FVIII interaction
Annals of Hematology, Vol. 75, Núm. 3, pp. 111-115
1996
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Antibodies to factor VIII in plasma of patients with hemophilia A and normal subjects
Annals of Hematology, Vol. 72, Núm. 5, pp. 321-326