José Pardos-Gea

Vall d'Hebron Research Institute

Spain

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Articles (17)

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2021

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2021

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2021

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2021

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2020

Collaborators (9)

Itziar Astigarraga

Profesora Asociada

Universidad del País Vasco Facultad de Farmacia

SPAIN

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ANNA ARNAU

SPAIN

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CHARY LOPEZ-PEDRERA

Head of Research

SPAIN

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Mª Dolors Tassies Penella

Institut d'Investigacions Biomèdiques August Pi i Sunyer

SPAIN

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José María Bastida

SPAIN

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Cecilia Chighizola

Associate Professor

University of Milan

ITALY

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Paul R. Fortin

Université Laval Faculté de médecine

CANADA

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Enrique Esteve-Valverde

Institute of Research and Innovation Parc Tauli

SPAIN

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Jaume Alijotas-Reig

Universitat Autònoma de Barcelona (UAB)

SPAIN

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José Pardos-Gea

Research Interests

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Articles (17)

Thrombosis recurrence and major bleeding in non-anticoagulated thrombotic antiphospholipid syndrome patients: Prospective study from antiphospholipid syndrome alliance for clinical trials and international networking (APS ACTION) clinical database and repository (“Registry”)

Thrombosis recurrence and major bleeding in non-anticoagulated thrombotic antiphospholipid syndrome patients: Prospective study from antiphospholipid syndrome alliance for clinical trials and international networking (APS ACTION) clinical database and repository ("Registry")

Fluctuation of Anti–Domain 1 and Anti–β2‐Glycoprotein I Antibody Titers Over Time in Patients With Persistently Positive Antiphospholipid Antibodies

Low complement levels are related to poor obstetric outcomes in women with obstetric antiphospholipid syndrome. The EUROAPS Registry Study Group

Anti–Neutrophil Extracellular Trap Antibodies in Antiphospholipid Antibody–Positive Patients: Results From the Antiphospholipid Syndrome Alliance for Clinical Trials and <scp>InternatiOnal</scp> Networking Clinical Database and Repository

Key Genes of the Immune System and Predisposition to Acquired Hemophilia A: Evidence from a Spanish Cohort of 49 Patients Using Next-Generation Sequencing

Correspondence on '2023 ACR/EULAR antiphospholipid syndrome classification criteria'

Corrigendum to “Low complement levels are related to poor obstetric outcomes in women with obstetric antiphospholipid syndrome. The EUROAPS Registry Study Group” [Placenta. 136 (2023 Apr 3) 29–34] (Placenta (2023) 136 (29–34), (S0143400423000723), (10.1016/j.placenta.2023.04.001))

Key Genes of the Immune System and Predisposition to Acquired Hemophilia A: Evidence from a Spanish Cohort of 49 Patients Using Next-Generation Sequencing

Severe bleeding diathesis as onset of light-chain amyloidosis: combined excessive fibrinolysis and acquired von Willebrand disease in a young patient

Pathogenesis, Diagnosis and Management of Obstetric Antiphospholipid Syndrome: A Comprehensive Review

Persistent thrombocytopenia predicts poor long-term survival in patients with antiphospholipid syndrome: a 38-year follow-up study.

Management of acquired hemophilia A: results from the Spanish registry

DERMATOMYOSITIS.

Proteomics and enriched biological processes in Antiphospholipid syndrome: A systematic review.

Bleeding and antithrombotic therapy during pregnancy in women with poor aPL-related obstetric outcomes: A survey of 1075 cases from EUROAPS registry∗.

Immunomodulatory therapy for the management of severe COVID-19. Beyond the anti-viral therapy: A comprehensive review.

Collaborators (9)

Itziar Astigarraga

ANNA ARNAU

CHARY LOPEZ-PEDRERA

Mª Dolors Tassies Penella

José María Bastida

Cecilia Chighizola

Paul R. Fortin

Enrique Esteve-Valverde

Jaume Alijotas-Reig

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