A. Pérez-Rodríguez

发表

Autosomal dominant C1149R von Willebrand disease: phenotypic findings and their implications

J. Batlle, A. Pérez-Rodríguez, A. García-Rivero, 2009, Haematologica.

Highlights in the diagnosis of type 1 von Willebrand disease

J. Batlle, A. Pérez-Rodríguez, M. López-Fernández, 2012 .

Diagnosis and management of von willebrand disease in Spain

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

Diagnosis and management of von Willebrand disease in Spain.

J. Batlle, A. Pérez-Rodríguez, J. Pinto, 2011, Seminars in thrombosis and hemostasis.

Classification of von Willebrand Disease

J. Batlle, A. Pérez-Rodríguez, M. López-Fernández, 2011 .

Acquired von Willebrand syndrome and mitral valve prosthesis leakage. A pilot study

J. Batlle, A. Pérez-Rodríguez, E. Lourés, 2011, European journal of haematology.

Challenging treatment for refractory acquired haemophilia A complicated with severe severe acute respiratory coronavirus 2 infection

A. Pérez-Rodríguez, M. F. Fernández, Tamara Lado Cives, 2022, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review.

J. Batlle, A. Pérez-Rodríguez, A. García-Rivero, 2014, Thrombosis research.

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.

Update on Molecular Testing in von Willebrand Disease

J. Batlle, F. Vidal, A. Pérez-Rodríguez, 2019, Seminars in Thrombosis and Hemostasis.

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.

Diagnosis of inherited von Willebrand disease: comparison of two methodologies and analysis of the discrepancies

J. Batlle, A. Pérez-Rodríguez, E. Lourés, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

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.

Type 2M von Willebrand disease: a variant of type 2A?

J. Batlle, A. Pérez-Rodríguez, M. López-Fernández, 2008, Journal of thrombosis and haemostasis : JTH.

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.

von Willebrand disease R1374C: Type 2A or 2M? A challenge to the revised classification. High frequency in the northwest of Spain (Galicia)

J. Batlle, A. Pérez-Rodríguez, E. Lourés, 2005, American journal of hematology.

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.

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.