Á. Rodríguez-Trillo

发表

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

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

Uncovering Cellular retinoic acid-binding protein 2 as a potential target for rheumatoid arthritis synovial hyperplasia

Antonio González, A. Mera-Varela, C. Conde, 2018, Scientific Reports.

HOXA5 is a key regulator of class 3 semaphorins expression in the synovium of rheumatoid arthritis patients

D. Veale, U. Fearon, J. Pego-Reigosa, 2022, Rheumatology.

Non-Canonical WNT5A Signaling Through RYK Contributes to Aggressive Phenotype of the Rheumatoid Fibroblast-Like Synoviocytes

Antonio González, A. Mera-Varela, C. Conde, 2020, Frontiers in Immunology.

ROCK inhibition with Y-27632 reduces joint inflammation and damage in serum-induced arthritis model and decreases in vitro osteoclastogenesis in patients with early arthritis

E. Pérez-Pampín, A. Mera-Varela, C. Conde, 2022, Frontiers in Immunology.

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.

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

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

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.

Diagnosis and management of von willebrand disease in Spain

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

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.

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.

Central Role of Semaphorin 3B in a Serum‐Induced Arthritis Model and Reduced Levels in Patients With Rheumatoid Arthritis

Á. González-Fernández, D. Veale, U. Fearon, 2022, Arthritis & rheumatology.

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

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

Assessment of mesenchymal stem/stromal cell-based therapy in K/BxN serum transfer-induced arthritis

C. Conde, M. Lopez-Santalla, M. Garin, 2022, Frontiers in Immunology.

All-Trans Retinoic Acid Inhibits Migration and Invasiveness of Rheumatoid Fibroblast-Like Synoviocytes

Antonio González, A. Mera-Varela, F. Blanco, 2019, The Journal of Pharmacology and Experimental Therapeutics.