Javier Batlle
A Coruna, GA, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
IX international curse of continuing formation in haemophilia and other congenital coagulopathies. The role of the Laboratory in coagulation disorders. Diagnosis of von Willebrand disease.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: November 16, 2021
Type 2N VWD: Conclusions from the Spanish PCM-EVW-ES project.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: May 13, 2021
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.
Journal: Thrombosis and haemostasis
Published: March 06, 2020
Update on Molecular Testing in von Willebrand Disease.
Journal: Seminars in thrombosis and hemostasis
Published: May 02, 2019
Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA.
Journal: Haematologica
Published: August 03, 2018
Role of multimeric analysis of von Willebrand factor (VWF) in von Willebrand disease (VWD) diagnosis: Lessons from the PCM-EVW-ES Spanish project.
Journal: PloS one
Published: February 20, 2018
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients.
Journal: Haematologica
Published: March 16, 2017
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): Proposal for a new diagnostic paradigm.
Journal: Thrombosis and haemostasis
Published: April 06, 2015
Diagnosis of inherited von Willebrand disease: comparison of two methodologies and analysis of the discrepancies.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: August 01, 2014
Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review.
Journal: Thrombosis research
Published: July 22, 2014
A novel mutation in ADAMTS13 of a child with Upshaw-Schulman Syndrome.
Journal: Thrombosis and haemostasis
Published: February 07, 2014
Last Updated: 09/26/2026