María Tenorio

Two Novel Mutations (HBG1: c.-250C>T and HBG2: c.-250C>T) Associated With Hereditary Persistence of Fetal Hemoglobin

S. Thein, B. Clark, S. Toma, 2014, Hemoglobin.

Transfusion support in COVID‐19 patients: Impact on hospital blood component supply during the outbreak

K. Velázquez-Kennedy, Alejandro Luna, María Tenorio, 2020, Transfusion.

Diagnosis and management of von willebrand disease in Spain

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

Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait

A. Muriel, F. Cava, J. Villarrubia, 2016, Journal of Clinical Pathology.

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.

Phenotype of mutations in the promoter region of the β-globin gene

B. Arrizabalaga, P. Ropero, M. Torrejón, 2017, Journal of Clinical Pathology.

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.

Use of eltrombopag for secondary immune thrombocytopenia in clinical practice

J. González-Porras, M. Álvarez‐Román, M. Gómez‐Nuñez, 2017, British journal of haematology.