Hematoloxía
Servicio
Leiden University Medical Center
Leiden, HolandaPublicacións en colaboración con investigadores/as de Leiden University Medical Center (21)
2023
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Integrating biological HLA-DPB1 mismatch models to predict survival after unrelated hematopoietic cell transplantation
Haematologica
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von Willebrand factor neutralizing and non-neutralizing alloantibodies in 213 subjects with type 3 von Willebrand disease enrolled in 3WINTERS-IPS
Journal of Thrombosis and Haemostasis, Vol. 21, Núm. 4, pp. 787-799
2022
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Eltrombopag Added to Immunosuppression in Severe Aplastic Anemia
New England Journal of Medicine, Vol. 386, Núm. 1, pp. 11-23
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Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study
Journal of Thrombosis and Haemostasis, Vol. 20, Núm. 5, pp. 1106-1114
2020
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Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease: Results from 3WINTERS-IPS, an international and collaborative cross-sectional study
Journal of Thrombosis and Haemostasis, Vol. 18, Núm. 9, pp. 2145-2154
2015
2013
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VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease
Blood, Vol. 121, Núm. 12, pp. 2336-2339
2011
2010
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The impact of bleeding history, von willebrand factor and PFA-100® on the diagnosis of type 1 von willebrand disease: Results from the european study MCMDM-1VWD
British Journal of Haematology, Vol. 151, Núm. 3, pp. 245-251
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Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD
Thrombosis Research, Vol. 126, Núm. 3, pp. 227-231
2009
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Expression of 14 von Willebrand factor mutations identified in patients with type.1 von Willebrand disease from the MCMDM-1VWD study
Journal of Thrombosis and Haemostasis, Vol. 7, Núm. 8, pp. 1304-1312
2008
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Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)
Journal of Thrombosis and Haemostasis, Vol. 6, Núm. 5, pp. 762-771
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Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the european study: Molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD)
Blood, Vol. 111, Núm. 10, pp. 4979-4985
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Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): Results from the European Study MCMDM-1VWD
Blood, Vol. 111, Núm. 7, pp. 3531-3539
2007
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Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1VWD)
Journal of Thrombosis and Haemostasis, Vol. 5, Núm. 4, pp. 715-721
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Mutational analysis of the von Willebrand factor gene in type 1 von Willebrand disease using conformation sensitive gel electrophoresis: A comparison of fluorescent and manual techniques
Haematologica, Vol. 92, Núm. 4, pp. 550-553
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Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
Blood, Vol. 109, Núm. 1, pp. 112-121
2006
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A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1 VWD)
Journal of Thrombosis and Haemostasis, Vol. 4, Núm. 4, pp. 766-773
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Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD
Journal of Thrombosis and Haemostasis, Vol. 4, Núm. 4, pp. 774-782
2005
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The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: An international, multicenter study
Journal of Thrombosis and Haemostasis, Vol. 3, Núm. 12, pp. 2619-2626