Disease: Hemolytic uremic syndrome- atypical- childhood
- A 2-year-old boy with circulatory failure owing to streptococcal toxic shock syndrome: case report
- A Guide for Adult Nephrologists and Hematologists to Managing Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy in Teens Transitioning to Young Adults
- A new era in the diagnosis and treatment of atypical haemolytic uraemic syndrome
- Advances in our understanding of the pathogenesis of glomerular thrombotic microangiopathy
- Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutation
- Atypical (non-diarrhea-associated) hemolytic-uremic syndrome in childhood
- Atypical hemolytic and uremic syndrome associated with von Willebrand factor-cleaving protease (ADAMTS 13) deficiency in children
- Atypical hemolytic uremic syndrome
- Atypical hemolytic uremic syndrome induced by CblC subtype of methylmalonic academia: A case report and literature review
- Atypical hemolytic uremic syndrome triggered by varicella infection
- C3 mesangial proliferative glomerulonephritis initially presenting with atypical hemolytic uremic syndrome: a case report
- Cardiovascular complications in atypical haemolytic uraemic syndrome
- Case Report: C3 deficiency in two siblings
- Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome
- Combined pulmonary hypertension and renal thrombotic microangiopathy in cobalamin C deficiency
- Complement deficiencies and dysregulation: Pathophysiological consequences, modern analysis, and clinical management
- Complement Dysregulation and Disease: Insights from Contemporary Genetics
- Complement factor H mutation associated with membranoproliferative glomerulonephritis with transformation to atypical haemolytic uraemic syndrome
- Eculizumab as rescue therapy for atypical hemolytic uremic syndrome with normal platelet count
- Eculizumab in paediatric atypical haemolytic uraemic syndrome: Lessons learned from a single-centre experience in the United Arab Emirates
- Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation
- Efficacy and safety of eculizumab in childhood atypical hemolytic uremic syndrome in Japan
- Epidemiology of haemolytic uremic syndrome in children. Data from the North Italian HUS network
- European best practice guidelines for renal transplantation. Section IV: Long-term management of the transplant recipient. IV.11 Paediatrics (specific problems)
- Extra-Renal manifestations of atypical hemolytic uremic syndrome in children
- Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland
- Factors determining penetrance in familial atypical haemolytic uraemic syndrome
- Familial, recurring plasma infusion dependent thrombotic thrombocytopenic purpura/hemolytic uremic syndrome
- Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome
- Genetics and CKD
- Genetics and genetic testing in hemolytic uremic syndrome/thrombotic thrombocytopenic purpura
- Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults
- Genetics of hemolytic uremic syndromes
- Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome
- Hemolytic and uremic syndrome and maternal-fetal Escherichia coli K1 infection
- Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
- Hemolytic uremic syndromes in childhood
- Hemolytic-Uremic Syndrome in childhood
- Hemolytic-uremic syndrome in Switzerland: a nationwide surveillance 1997-2003
- Hemolytic-Uremic Syndrome in Uberlandia, MG, Brazil
- HUS and TTP: traversing the disease and the age spectrum
- Hypoproteinemia in the hemolytic-uremic syndrome of childhood
- Incomplete penetrance of CD46 mutation causing familial atypical hemolytic uremic syndrome
- Novel aspects of atypical haemolytic uraemic syndrome and the role of eculizumab
- Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children
- Pathophysiology and management of thrombotic microangiopathies
- Prophylactic eculizumab prior to kidney transplantation for atypical hemolytic uremic syndrome
- Recurrent Atypical Hemolytic Uremic Syndrome in Children With Acute Lymphoblastic Leukemia Undergoing Maintenance Chemotherapy
- Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children
- Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
- Renal recovery with eculizumab in atypical hemolytic uremic syndrome following prolonged dialysis
- Severe pneumococcal hemolytic uremic syndrome in an 8-month-old girl
- Survey of haemolytic-uraemic syndrome in Queensland 1979-1995
- The causes and consequences of paediatric kidney disease on adult nephrology care
- The haemolytic-uraemic syndrome in childhood
- The polymorphonuclear leucocyte count in childhood haemolytic uraemic syndrome
- The Role of the Complement System in the Pathogenesis of Infectious Forms of Hemolytic Uremic Syndrome
- Thrombotic microangiopathies: thrombotic thrombocytopenic purpura / hemolytic uremic syndrome
- Thrombotic microangiopathy and associated renal disorders
- Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura
- Thrombotic microangiopathy: focus on atypical hemolytic uremic syndrome
- Thrombotic thrombocytopenic purpura in childhood: an uncommon but life-threatening cause of thrombocytopenia
- Treatment and outcome of Shiga-toxin-associated hemolytic uremic syndrome (HUS)
- Treatment of Congenital Thrombotic Thrombocytopenic Purpura With Eculizumab
- Treatment of hemolytic uremic syndrome
- Typical and atypical hemolytic uremic syndrome
- Ulcerative Colitis and Atypical Hemolytic-Uremic Syndrome: An Unusual But Potentially Life-threatening Complication
- Various phenotypes of disease associated with mutated DGKE gene
- von Willebrand factor-cleaving protease in childhood diarrhoea-associated haemolytic uraemic syndrome
- Whole exome sequencing identifies monogenic forms of nephritis in a previously unsolved cohort of children with steroid-resistant nephrotic syndrome and hematuria