Francisco Javier
Batlle Fonrodona
Hospital Universitario Marqués de Valdecilla
Santander, EspañaPublicacións en colaboración con investigadores/as de Hospital Universitario Marqués de Valdecilla (12)
2021
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Type 2N VWD: Conclusions from the Spanish PCM-EVW-ES project
Haemophilia, Vol. 27, Núm. 6, pp. 1007-1021
2020
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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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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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Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): A short review
Thrombosis Research, Vol. 134, Núm. 6, pp. 1171-1175
2005
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Psychometric field study of the new haemophilia quality of life questionnaire for adults: The 'Hemofilia-QoL'
Haemophilia, Vol. 11, Núm. 6, pp. 603-610
2004
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Development of a new disease-specific quality-of-life questionnaire to adults living with haemophilia
Haemophilia, Vol. 10, Núm. 4, pp. 376-382
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
1990
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Acquired von willebrand disease in multiple myeloma secondary to absorption of von willebrand factor by plasma cells
American Journal of Hematology, Vol. 35, Núm. 2, pp. 114-117