How I treat: the clinical differentiation and initial treatment of adult patients with atypical hemolytic uremic syndrome

Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy

(2013) S. Jodele et al.   BLOOD

Complement activation in diseases presenting with thrombotic microangiopathy

(2013) Seppo Meri   European Journal of Internal Medicine

Urinary Excretion of C5b-9 in Severe Preeclampsia

(2013) Richard M. Burwick et al.   HYPERTENSION

Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome

(2013) F. Bu et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

(2013) E. Bresin et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

(2013) Mathieu Lemaire et al.   NATURE GENETICS

Terminal Complement Inhibitor Eculizumab in Atypical Hemolytic–Uremic Syndrome

(2013) C.M. Legendre et al.   NEW ENGLAND JOURNAL OF MEDICINE

Neurologic involvement in atypical hemolytic uremic syndrome and successful treatment with eculizumab

(2013) Kaan Gulleroglu et al.   PEDIATRIC NEPHROLOGY

Assembly and Activation of Alternative Complement Components on Endothelial Cell-Anchored Ultra-Large Von Willebrand Factor Links Complement and Hemostasis-Thrombosis

(2013) Nancy A. Turner et al.   PLoS One

Performance of a clinical prediction score for thrombotic thrombocytopenic purpura in an independent cohort

(2013) M. J. Bentley et al.   VOX SANGUINIS

Profound neurological injury in a patient with atypical hemolytic uremic syndrome

(2012) Galena Salem et al.   ANNALS OF HEMATOLOGY

Relapse of aHUS after discontinuation of therapy with eculizumab in a patient with aHUS and factor H mutation

(2012) Ryan Carr et al.   ANNALS OF HEMATOLOGY

The use of ADAMTS13 activity, platelet count, and serum creatinine to differentiate acquired thrombotic thrombocytopenic purpura from other thrombotic microangiopathies

(2012) Spero R. Cataland et al.   BRITISH JOURNAL OF HAEMATOLOGY

Complement activation in thrombotic thrombocytopenic purpura

(2012) M. RÉTI et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

STEC-HUS, atypical HUS and TTP are all diseases of complement activation

(2012) Marina Noris et al.   Nature Reviews Nephrology

Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

(2012) Julien Zuber et al.   Nature Reviews Nephrology

Acquired Idiopathic ADAMTS13 Activity Deficient Thrombotic Thrombocytopenic Purpura in a Population from Japan

(2012) Masanori Matsumoto et al.   PLoS One

Clinical features of severe acquired ADAMTS13 deficiency in thrombotic thrombocytopenic purpura: the Korean TTP registry experience

(2011) Moon Ju Jang et al.   INTERNATIONAL JOURNAL OF HEMATOLOGY

Atypical hemolytic uremic syndrome

(2011) Chantal Loirat et al.   Orphanet Journal of Rare Diseases

Insufficient protection by Neisseria meningitidis vaccination alone during eculizumab therapy

(2011) Antonia Bouts et al.   PEDIATRIC NEPHROLOGY

Mutations in Complement Regulatory Proteins Predispose to Preeclampsia: A Genetic Analysis of the PROMISSE Cohort

(2011) Jane E. Salmon et al.   PLOS MEDICINE

Pulse Cyclophosphamide Therapy and Clinical Remission in Atypical Hemolytic Uremic Syndrome With Anti–Complement Factor H Autoantibodies

(2010) Olivia Boyer et al.   AMERICAN JOURNAL OF KIDNEY DISEASES

Thrombotic Microangiopathy After Kidney Transplantation

(2010) M. Noris et al.   AMERICAN JOURNAL OF TRANSPLANTATION

How I treat patients with thrombotic thrombocytopenic purpura: 2010

(2010) J. N. George   BLOOD

Review of Meningococcal Group B Vaccines

(2010) Dan M. Granoff   CLINICAL INFECTIOUS DISEASES

Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

(2010) M. Noris et al.   Clinical Journal of the American Society of Nephrology

Clinical Features of Anti-Factor H Autoantibody-Associated Hemolytic Uremic Syndrome

(2010) M.-A. Dragon-Durey et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Advances in the Development of Vaccines againstNeisseria meningitidis

(2010) Lionel K.K. Tan et al.   NEW ENGLAND JOURNAL OF MEDICINE

Predictive Features of Severe Acquired ADAMTS13 Deficiency in Idiopathic Thrombotic Microangiopathies: The French TMA Reference Center Experience

(2010) Paul Coppo et al.   PLoS One

Plasmatherapy in Atypical Hemolytic Uremic Syndrome

(2010) Chantal Loirat et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

The utility of patient characteristics in predicting severe ADAMTS13 deficiency and response to plasma exchange

(2010) Melissa J. Bentley et al.   TRANSFUSION

Clinical Practice Guidelines for the management of atypical Haemolytic Uraemic Syndrome in the United Kingdom

(2009) C. Mark Taylor et al.   BRITISH JOURNAL OF HAEMATOLOGY

Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome

(2009) Frank Bienaime et al.   KIDNEY INTERNATIONAL

Functional analyses indicate a pathogenic role of factor H autoantibodies in atypical haemolytic uraemic syndrome

(2009) S. Strobel et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Atypical Hemolytic–Uremic Syndrome

(2009) Marina Noris et al.   NEW ENGLAND JOURNAL OF MEDICINE

Atypical Hemolytic Uremic Syndrome Associated With Complement Factor H Autoantibodies and CFHR1/CFHR3 Deficiency

(2009) Beom Hee Lee et al.   PEDIATRIC RESEARCH

Interventions for Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura: A Systematic Review of Randomized Controlled Trials

(2008) Mini Michael et al.   AMERICAN JOURNAL OF KIDNEY DISEASES

Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura

(2008) J. E. Sadler   BLOOD

Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome

(2008) Gema Ariceta et al.   PEDIATRIC NEPHROLOGY

Complement and the atypical hemolytic uremic syndrome in children

(2008) Chantal Loirat et al.   PEDIATRIC NEPHROLOGY