Complement Activation and Thrombotic Microangiopathies (original) (raw)

Complement in Secondary Thrombotic Microangiopathy

Sanjeev Sethi

Kidney International Reports

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Complement Factor C4d Is a Common Denominator in Thrombotic Microangiopathy

J de Fijter

Journal of the American Society of Nephrology : JASN, 2015

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Complement activation and blockade in massive post-partum haemorrhage, thrombotic microangiopathy and acute kidney injury: a case report

Gabriella Guzzo

BMC Nephrology, 2021

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Novel biomarker and easy to perform ELISA for monitoring complement inhibition in patients with atypical hemolytic uremic syndrome treated with eculizumab

ALEJANDRA ANDRADE ROSALES

Journal of Immunological Methods, 2016

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The Alternative Pathway of Complement and the Evolving Clinical-Pathophysiological Spectrum of Atypical Hemolytic Uremic Syndrome

Bruce Berger

The American journal of the medical sciences, 2016

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Atypical hemolytic-uremic syndrome: the interplay between complements and the coagulation system

Arif Asif

Iranian journal of kidney diseases, 2013

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Spectrum of Complement-Mediated Thrombotic Microangiopathies: Pathogenetic Insights Identifying Novel Treatment Approaches

Magdalena Riedl, Damien Noone

Seminars in Thrombosis and Hemostasis, 2014

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Patients with hypertension-associated thrombotic microangiopathy may present with complement abnormalities

Frank Stifft

Kidney international, 2017

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Too much of a good thing at the site of tissue injury: the instructive example of the complement system predisposing to thrombotic microangiopathy

Patty Atkinson

Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program, 2011

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Evaluation of complement regulatory components in patients with atypical hemolytic uremic syndrome

Akbar Dorgalaleh

Central European Journal of Immunology, 2014

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Direct evidence of complement activation in HELLP syndrome: A link to atypical hemolytic uremic syndrome

Eleni Gavriilaki

Experimental Hematology, 2016

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Complement in hemolytic anemia

R. Brodsky

Blood, 2015

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Extra-Renal Manifestations of Complement-Mediated Thrombotic Microangiopathies

Alejandra Rosales

Frontiers in Pediatrics, 2014

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Complement-mediated thrombotic microangiopathy secondary to sepsis-induced disseminated intravascular coagulation successfully treated with eculizumab

Everardo Torres

Medicine, 2017

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Complement activation in thrombotic thrombocytopenic purpura

K. Rázsó, M. Réti

Journal of Thrombosis and Haemostasis, 2012

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Complement activation by heme as a secondary hit for atypical hemolytic uremic syndrome

Fanny Tabarin

Blood, 2013

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Complement Activation During Liver Transplantation—Special Emphasis on Patients With Atypical Hemolytic Uremic Syndrome

Arno Nordin

American Journal of Transplantation, 2011

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Screening for Complement System Abnormalities in Patients with Atypical Hemolytic Uremic Syndrome

Marina Noris

Clinical Journal of the American Society of Nephrology, 2007

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Thrombotic Microangiopathies and the Linkage between von Willebrand Factor and the Alternative Complement Pathway

Jennifer Nolasco

Thrombotic Microangiopathies and the Linkage between von Willebrand Factor and the Alternative Complement Pathway

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Complement component 5 promotes lethal thrombosis

Tomoyuki Okuda

Scientific Reports, 2017

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An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome

Annalisa Perna

American Journal of Kidney Diseases, 2019

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Complement Activation Induces Neutrophil Adhesion and Neutrophil-Platelet Aggregate Formation on Vascular Endothelial Cells

Christoph Licht

Kidney International Reports, 2017

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C3 Glomerulopathy and Atypical Hemolytic Uremic Syndrome: Two Important Manifestations of Complement System Dysfunction

Taimoor Ashraf Khan

Case reports in nephrology and dialysis

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ORIGINAL ARTICLE: Human Serum Complement C3 and Factor H in the Syndrome of Hemolysis, Elevated Liver Enzymes, and Low Platelet Count

Elif Ari Bakir

American Journal of Reproductive Immunology, 2009

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Eculizumab reduces complement activation, inflammation, endothelial damage, thrombosis, and renal injury markers in aHUS

R. Cofiell

Blood, 2015

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Complement Activation Associated with ADAMTS13 Deficiency in Human and Murine Thrombotic Microangiopathy

Anne-lie Ståhl

The Journal of Immunology, 2013

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Measurement of complement activation via plasma soluble C5b-9 comparison with terminal complement complex staining in a series of kidney biopsies

Carolyn Wijaya

Kidney and Blood Pressure Research

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In vitro evidence of complement activation in transplantation-associated thrombotic microangiopathy

Eleni Gavriilaki

Blood Advances, 2017

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Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

Ronny Decorte

Proceedings of the National Academy of Sciences, 2003

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Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation

F. Vaziri-Sani

Blood, 2008

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Complement Activation in Arterial and Venous Thrombosis is Mediated by Plasmin

Kimberley Foley

EBioMedicine, 2016

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