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Complement Overactivation and Consumption Predicts In-Hospital Mortality in SARS-CoV-2 Infection

Frontiers in immunology, 2021-03, Vol.12, p.663187-663187

2021

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Complement analysis 2016: Clinical indications, laboratory diagnostics and quality control

Immunobiology (1979), 2016-11, Vol.221 (11), p.1247-1258

2016

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Expanding Horizons in Complement Analysis and Quality Control

Frontiers in immunology, 2021-08, Vol.12, p.697313-697313

2021

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Red cell distribution width in heart failure: Prediction of clinical events and relationship with markers of ineffective erythropoiesis, inflammation, renal function, and nutritional state

The American heart journal, 2009-10, Vol.158 (4), p.659-666

2009

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Class switch towards spike protein-specific IgG4 antibodies after SARS-CoV-2 mRNA vaccination depends on prior infection history

Scientific reports, 2023-08, Vol.13 (1), p.13166-13166, Article 13166

2023

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Editorial: Complement and COVID-19 Disease

Frontiers in immunology, 2022-07, Vol.13, p.960809-960809

2022

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Activation of the complement system in normal pregnancy and preeclampsia

Molecular immunology, 2010-04, Vol.47 (7), p.1500-1506

2010

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Evidence, detailed characterization and clinical context of complement activation in acute multisystem inflammatory syndrome in children

Scientific reports, 2022-11, Vol.12 (1), p.19759-19759, Article 19759

2022

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Associations between the von Willebrand Factor-ADAMTS13 Axis, Complement Activation, and COVID-19 Severity and Mortality

Thrombosis and haemostasis, 2022-02, Vol.122 (2), p.240-256

2022

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Complement Protease MASP-1 Activates Human Endothelial Cells: PAR4 Activation Is a Link between Complement and Endothelial Function

The Journal of immunology (1950), 2009-09, Vol.183 (5), p.3409-3416

2009

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Circulating mortalin in blood and activation of the alternative complement pathway as risk indicators in COVID-19 infection

Frontiers in immunology, 2024-04, Vol.15, p.1337215-1337215

2024

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External quality assurance program for diagnostic complement laboratories: evaluation of the results of the past seven years

Frontiers in immunology, 2024-03, Vol.15, p.1368399-1368399

2024

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The role of the complement system in hereditary angioedema

Molecular immunology, 2017-09, Vol.89, p.59-68

2017

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Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura

Blood, 2021-06, Vol.137 (25), p.3563-3575

2021

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Atypical hemolytic uremic syndrome triggered by mRNA vaccination against SARS-CoV-2: Case report

Frontiers in immunology, 2022-09, Vol.13, p.1001366

2022

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Natural Autoantibodies in Biologic-Treated Rheumatoid Arthritis and Ankylosing Spondylitis Patients: Associations with Vascular Pathophysiology

International journal of molecular sciences, 2024-03, Vol.25 (6), p.3429

2024

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Anti-Inflammatory Cytokine Profiles in Thrombotic Thrombocytopenic Purpura-Differences Compared to COVID-19

International journal of molecular sciences, 2024-09, Vol.25 (18), p.10007

2024

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MCPggaac haplotype is associated with poor graft survival in kidney transplant recipients with de novo thrombotic microangiopathy

Frontiers in immunology, 2022-09, Vol.13, p.985766-985766

2022

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Immunosuppressive Therapy of Antibody-Mediated aHUS and TTP

International journal of molecular sciences, 2023-09, Vol.24 (18), p.14389

2023

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Atypical HUS and Crohn’s disease—interference of intestinal disease activity with complement-blocking treatment

Pediatric nephrology (Berlin, West), 2021-10, Vol.36 (10), p.3277-3280

2021

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COVID-19: a trigger for severe thrombotic microangiopathy in a patient with complement gene variant

Romanian Journal of Internal Medicine, 2022-06, Vol.60 (2), p.138-142

2022

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Complement activation, inflammation and relative ADAMTS13 deficiency in secondary thrombotic microangiopathies

Immunobiology (1979), 2017-02, Vol.222 (2), p.119-127

2017

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Complement Genetic Variants and FH Desialylation in S. pneumoniae -Haemolytic Uraemic Syndrome

Frontiers in immunology, 2021-03, Vol.12, p.641656-641656

2021

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Storage of Transfusion Platelet Concentrates Is Associated with Complement Activation and Reduced Ability of Platelets to Respond to Protease-Activated Receptor-1 and Thromboxane A2 Receptor

International journal of molecular sciences, 2024-01, Vol.25 (2), p.1091

2024

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Autoantibodies Against the Complement Regulator Factor H in the Serum of Patients With Neuromyelitis Optica Spectrum Disorder

Frontiers in immunology, 2021-04, Vol.12, p.660382-660382

2021

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Complement Overactivation and Consumption Predicts In-Hospital Mortality in SARS-CoV-2 Infection

Complement analysis 2016: Clinical indications, laboratory diagnostics and quality control

Expanding Horizons in Complement Analysis and Quality Control

Red cell distribution width in heart failure: Prediction of clinical events and relationship with markers of ineffective erythropoiesis, inflammation, renal function, and nutritional state

Class switch towards spike protein-specific IgG4 antibodies after SARS-CoV-2 mRNA vaccination depends on prior infection history

Editorial: Complement and COVID-19 Disease

Activation of the complement system in normal pregnancy and preeclampsia

Evidence, detailed characterization and clinical context of complement activation in acute multisystem inflammatory syndrome in children

Associations between the von Willebrand Factor-ADAMTS13 Axis, Complement Activation, and COVID-19 Severity and Mortality

Complement Protease MASP-1 Activates Human Endothelial Cells: PAR4 Activation Is a Link between Complement and Endothelial Function

Circulating mortalin in blood and activation of the alternative complement pathway as risk indicators in COVID-19 infection

External quality assurance program for diagnostic complement laboratories: evaluation of the results of the past seven years

The role of the complement system in hereditary angioedema

Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura

Atypical hemolytic uremic syndrome triggered by mRNA vaccination against SARS-CoV-2: Case report

Natural Autoantibodies in Biologic-Treated Rheumatoid Arthritis and Ankylosing Spondylitis Patients: Associations with Vascular Pathophysiology

Anti-Inflammatory Cytokine Profiles in Thrombotic Thrombocytopenic Purpura-Differences Compared to COVID-19

MCPggaac haplotype is associated with poor graft survival in kidney transplant recipients with de novo thrombotic microangiopathy

Immunosuppressive Therapy of Antibody-Mediated aHUS and TTP

Atypical HUS and Crohn’s disease—interference of intestinal disease activity with complement-blocking treatment

COVID-19: a trigger for severe thrombotic microangiopathy in a patient with complement gene variant

Complement activation, inflammation and relative ADAMTS13 deficiency in secondary thrombotic microangiopathies

Complement Genetic Variants and FH Desialylation in S. pneumoniae -Haemolytic Uraemic Syndrome

Storage of Transfusion Platelet Concentrates Is Associated with Complement Activation and Reduced Ability of Platelets to Respond to Protease-Activated Receptor-1 and Thromboxane A2 Receptor

Autoantibodies Against the Complement Regulator Factor H in the Serum of Patients With Neuromyelitis Optica Spectrum Disorder

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