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

Arthritis & rheumatology (Hoboken, N.J.), 2023-08, Vol.75 (8), p.1407-1414

2023

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Associations Among Antiphospholipid Antibody Types, Isotypes, and Titers: An AntiPhospholipid Syndrome Alliance for Clinical Trials and InternatiOnal Networking (APS ACTION) Study

Laboratory investigation, 2023-06, Vol.103 (6), p.100147-100147, Article 100147

2023

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Fluctuation of Anti-Domain 1 and Anti-β 2 -Glycoprotein I Antibody Titers Over Time in Patients With Persistently Positive Antiphospholipid Antibodies

Arthritis & rheumatology (Hoboken, N.J.), 2023-06, Vol.75 (6), p.984-995

2023

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Retroperitoneal and lower extremities muscle bleeding in acquired haemophilia A ( AHA ): Risk factors and implications in disability and survival

European journal of haematology, 2024-07

2024

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Positive prayer sign in eosinophilic fasciitis

Rheumatology (Oxford, England), 2017-04, Vol.56 (4), p.628-628

Pardos-Gea, José

2017

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

Rheumatology (Oxford, England), 2022-03, Vol.61 (3), p.1053-1061

2022

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Cardiac manifestations other than valvulopathy in antiphospholipid syndrome: long-time echocardiography follow-up study

International journal of rheumatic diseases, 2015-01, Vol.18 (1), p.76-83

2015

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Protein Z and atherosclerotic disease: a less close relationship than though

Journal of thrombosis and thrombolysis, 2017-04, Vol.43 (3), p.387-389

Pardos-Gea, José

2017

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

Blood coagulation & fibrinolysis, 2023-01, Vol.34 (1), p.79

2023

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

Arthritis & rheumatology (Hoboken, N.J.), 2023-06, Vol.75 (6), p.984-995

2023

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IgG4-Related Disease: Results From a Multicenter Spanish Registry

Medicine (Baltimore), 2015-08, Vol.94 (32), p.e1275-e1275

2015

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

International journal of molecular sciences, 2023-11, Vol.24 (22), p.16372

2023

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Acquired von Willebrand syndrome in a patient with small lymphocytic lymphoma and Sjögren's syndrome: which associated condition should be prioritized?

Blood coagulation & fibrinolysis, 2019-07, Vol.30 (5), p.239-242

2019

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Autoantibodies to types I and IV collagen and heart valve disease in systemic lupus erythematosus/antiphospholipid syndrome

Clinical rheumatology, 2017-06, Vol.36 (6), p.1401-1406

2017

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Protein Z levels and anti-protein Z antibodies in patients with arterial and venous thrombosis

Thrombosis research, 2008-01, Vol.121 (6), p.727-734

2008

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Home intravenous antimicrobial therapy in multi-drug resistant microorganism infections

Medicina clinica, 2012-05, Vol.138 (13), p.557

2012

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Home intravenous antibiotic therapy of hepatic abscess: Safety, efficacy and predictive factor of hospital readmission

Medicina clínica, 2010-04, Vol.134 (11), p.473-476

2010

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Intravenous antibiotic treatment in a hospital based home care unit. Predictors of hospital readmission

Medicina clínica, 2008-09, Vol.131 (8), p.290-292

2008

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Home intravenous antibiotic therapy of empyema and lung abscess: safety and efficacy

Enfermedades infecciosas y microbiologia clinica, 2011-03, Vol.29 (3), p.237

2011

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

Annals of the rheumatic diseases, 2024-03, Vol.83 (3), p.e2-e2

2024

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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”)

Seminars in arthritis and rheumatism, 2024-04, Vol.65, p.152347-152347, Article 152347

2024

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Neutropenia autoinmunitaria crónica del adulto y su frecuente asociación con déficit de IgG. Estudio de un caso y revisión bibliográfica

Medicina clínica, 2015-12, Vol.145 (12), p.553-554

2015

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Survey on antiphospholipid syndrome diagnosis and antithrombotic treatment in patients with ischemic stroke, other brain ischemic injury, or arterial thromboembolism in other sites: communication from ISTH SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies

Journal of thrombosis and haemostasis, 2023-10, Vol.21 (10), p.2963-2976

2023

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Acquired haemophilia A: successful treatment with immunosuppression, methylprednisolone pulses and oral cyclosporin

Thrombosis and haemostasis, 2006-04, Vol.95 (4), p.735-737

2006

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

Damage measured by Damage Index for Antiphospholipid Syndrome (DIAPS) in antiphospholipid antibody-positive patients included in the APS ACTION registry

Associations Among Antiphospholipid Antibody Types, Isotypes, and Titers: An AntiPhospholipid Syndrome Alliance for Clinical Trials and InternatiOnal Networking (APS ACTION) Study

Fluctuation of Anti-Domain 1 and Anti-β 2 -Glycoprotein I Antibody Titers Over Time in Patients With Persistently Positive Antiphospholipid Antibodies

Retroperitoneal and lower extremities muscle bleeding in acquired haemophilia A ( AHA ): Risk factors and implications in disability and survival

Positive prayer sign in eosinophilic fasciitis

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

Cardiac manifestations other than valvulopathy in antiphospholipid syndrome: long-time echocardiography follow-up study

Protein Z and atherosclerotic disease: a less close relationship than though

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

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

IgG4-Related Disease: Results From a Multicenter Spanish Registry

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

Acquired von Willebrand syndrome in a patient with small lymphocytic lymphoma and Sjögren's syndrome: which associated condition should be prioritized?

Autoantibodies to types I and IV collagen and heart valve disease in systemic lupus erythematosus/antiphospholipid syndrome

Protein Z levels and anti-protein Z antibodies in patients with arterial and venous thrombosis

Home intravenous antimicrobial therapy in multi-drug resistant microorganism infections

Home intravenous antibiotic therapy of hepatic abscess: Safety, efficacy and predictive factor of hospital readmission

Intravenous antibiotic treatment in a hospital based home care unit. Predictors of hospital readmission

Home intravenous antibiotic therapy of empyema and lung abscess: safety and efficacy

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

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”)

Neutropenia autoinmunitaria crónica del adulto y su frecuente asociación con déficit de IgG. Estudio de un caso y revisión bibliográfica

Survey on antiphospholipid syndrome diagnosis and antithrombotic treatment in patients with ischemic stroke, other brain ischemic injury, or arterial thromboembolism in other sites: communication from ISTH SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies

Acquired haemophilia A: successful treatment with immunosuppression, methylprednisolone pulses and oral cyclosporin

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