S. Herrero

发表

Immunophenotypic analysis of mast cells in mastocytosis: When and how to do it. Proposals of the Spanish Network on Mastocytosis (REMA)

A. Órfão, J. Almeida, A. García-Montero, 2004, Cytometry. Part B, Clinical cytometry.

Diagnosis and management of von willebrand disease in Spain

V. Jiménez‐Yuste, J. Mateo, J. Batlle, 2018 .

A pilot study on the impact of congenital thrombophilia in COVID‐19

J. Corral, V. Vicente, A. Miñano, 2021, European journal of clinical investigation.

Human bone marrow mast cells from indolent systemic mast cell disease constitutively express increased amounts of the CD63 protein on their surface.

A. Órfão, J. S. San Miguel, A. Torrelo, 1998, Cytometry.

Role of multimeric analysis of von Willebrand factor (VWF) in von Willebrand disease (VWD) diagnosis: Lessons from the PCM-EVW-ES Spanish project

V. Jiménez‐Yuste, J. Mateo, J. Batlle, 2018, PloS one.

Activated Prothrombin Complex Concentrate to Treat Bleeding Events in Acquired Hemophilia A: Bahas Study.

M. Mingot-Castellano, R. Pérez-Montes, Olga Benítez Hidalgo, 2022, European journal of haematology.

Adherence to prophylaxis and quality of life in children and adolescents with severe haemophilia A

V. Jiménez‐Yuste, C. Altisent, J. Aznar, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Molecular and clinical profile of von Willebrand disease in Spain (PCM–EVW–ES): Proposal for a new diagnostic paradigm

V. Jiménez‐Yuste, J. Mateo, J. Batlle, 2015, Thrombosis and Haemostasis.

Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes

J. Hernández-Rivas, G. R. Ordóñez, M. González-Díaz, 2016, Thrombosis and Haemostasis.

Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients

V. Jiménez‐Yuste, J. Mateo, J. Batlle, 2017, Haematologica.

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

V. Jiménez‐Yuste, J. Mateo, J. Batlle, 2020, Thrombosis and Haemostasis.

One-step detection of c-kit point mutations using peptide nucleic acid-mediated polymerase chain reaction clamping and hybridization probes.

U. Lass, K. Sotlar, O. Landt, 2003, The American journal of pathology.

Type 2N VWD: Conclusions from the Spanish PCM‐EVW‐ES project

V. Jiménez‐Yuste, J. Mateo, J. Batlle, 2021, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of 58 Mutations (26 Novel) in 94 of 109 Symptomatic Spanish Probands with Protein C Deficiency

J. González-Porras, F. España, A. Vayá, 2019, Thrombosis and Haemostasis.

The CD69 early activation molecule is overexpressed in human bone marrow mast cells from adults with indolent systemic mast cell disease

A. Órfão, J. S. San Miguel, L. Escribano, 1999, British journal of haematology.

Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA

V. Jiménez‐Yuste, J. Mateo, J. Batlle, 2018, Haematologica.

Mantle cell lymphoma with amyotrophic lateral sclerosis (motor neuron disease)

J. Gobernado, C. Bellas, J. Pérez-Oteyza, 1998, Haematologica.