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Orphanet journal of rare diseases, ISSN 1750-1172, 2011, Volume 6, Issue 1, pp. 60 - 60
Hemolytic uremic syndrome (HUS) is defined by the triad of mechanical hemolytic anemia, thrombocytopenia and renal impairment. Atypical HUS (aHUS... 
Plasma exchange | Factor H | Combined liver-kidney transplantation | Plasma infusion | Factor B | Atypical hemolytic uremic syndrome | Eculizumab | Membrane cofactor protein | Thrombomodulin | Factor I | Kidney transplantation | MEDICINE, RESEARCH & EXPERIMENTAL | factor I | CFHR1/CFHR3 DEFICIENCY | LIVER-KIDNEY TRANSPLANTATION | plasma infusion | kidney transplantation | eculizumab | factor B | THROMBOTIC THROMBOCYTOPENIC PURPURA | SUCCESSFUL RENAL-TRANSPLANTATION | factor H | combined liver-kidney transplantation | INHIBITOR ECULIZUMAB | ALTERNATIVE PATHWAY | membrane cofactor protein | thrombomodulin | GENETICS & HEREDITY | plasma exchange | SUCCESSFUL PLASMA THERAPY | FACTOR-I MUTATIONS | COMPLEMENT-FACTOR-H | Complement Activation | Humans | Middle Aged | Child, Preschool | Complement System Proteins - immunology | Infant | Male | Hemolytic-Uremic Syndrome - epidemiology | Young Adult | Hemolytic-Uremic Syndrome - genetics | Hemolytic-Uremic Syndrome - physiopathology | Aged, 80 and over | Adult | Complement System Proteins - genetics | Female | Hemolytic-Uremic Syndrome - therapy | Child | Infant, Newborn | Risk Factors | Kidney Transplantation | Animals | Adolescent | Aged | Mice | Mutation | Atypical Hemolytic Uremic Syndrome | Viral antibodies | Usage | Care and treatment | Antibodies | Genetic aspects | Research | Diagnosis | Health aspects | Genetic screening | Hemolytic-uremic syndrome | Risk factors | Lupus | Plasma | E coli | Disease | Vascular endothelial growth factor | Streptococcus infections
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2009, Volume 361, Issue 17, pp. 1676 - 1687
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2013, Volume 368, Issue 23, pp. 2169 - 2181
Journal Article
Journal Article
Clinical journal of the American Society of Nephrology, ISSN 1555-905X, 2017, Volume 12, Issue 8, pp. 1237 - 1247
Background Pregnancy is associated with various forms of thrombotic microangiopathy, including hemolytic uremic syndrome... 
COFACTOR PROTEIN CD46 | AUTOANTIBODIES | FETOMATERNAL INTERFACE | CELLS | FACTOR-H MUTATIONS | GENE | RARE | COMPLEMENT INHIBITOR ECULIZUMAB | UROLOGY & NEPHROLOGY | DECAY-ACCELERATING FACTOR | Recurrence | Renal Insufficiency, Chronic - etiology | Humans | Middle Aged | Postpartum Period | Plasma Exchange | Genetic Variation | Young Adult | Hemolytic-Uremic Syndrome - genetics | Time Factors | Adult | Female | Hemolytic-Uremic Syndrome - therapy | Retrospective Studies | Complement Activation - drug effects | Genetic Predisposition to Disease | Antibodies, Monoclonal, Humanized - therapeutic use | Hemolytic-Uremic Syndrome - complications | Europe | Complement Factor I - genetics | Treatment Outcome | Hemolytic-Uremic Syndrome - immunology | Disease Progression | Pregnancy | Complement Activation - genetics | Phenotype | Adolescent | Complement Inactivating Agents - therapeutic use | Pregnancy Complications - genetics | Complement Factor H - genetics | Kidney Failure, Chronic - etiology | Pregnancy Complications - immunology | Pregnancy Complications - therapy | Renal Dialysis | chemotactic factor inactivator | Follow-Up Studies | pregnancy | kidney transplantation | Thrombotic Microangiopathies | United Kingdom | eculizumab | hemolytic uremic syndrome | Antibodies, Monoclonal, Humanized | Italy | Kidney Failure, Chronic | thrombotic microangiopathy | complement | Complement Pathway, Alternative | France | Original | Atypical Hemolytic Uremic Syndrome | renal dialysis
Journal Article
Kidney international, ISSN 0085-2538, 2017, Volume 91, Issue 3, pp. 539 - 551
Journal Article
Pediatric nephrology (Berlin, West), ISSN 1432-198X, 2015, Volume 31, Issue 1, pp. 15 - 39
Atypical hemolytic uremic syndrome (aHUS) emerged during the last decade as a disease largely of complement dysregulation... 
Pediatrics | Thrombotic microangiopathy | Nephrology | Hemolytic uremic syndrome | Complement | Urology | Plasma exchange | Plasma infusion | Medicine & Public Health | Anti-factor H antibody | Combined liver–kidney transplantation | Atypical hemolytic uremic syndrome | Eculizumab | Children | Kidney transplantation | ADULT PATIENTS | LIVER-KIDNEY TRANSPLANTATION | RENAL-TRANSPLANT | COMPLEMENT INHIBITOR ECULIZUMAB | CLINICAL CHARACTERISTICS | THROMBOTIC THROMBOCYTOPENIC PURPURA | FACTOR-H ANTIBODIES | Combined liver-kidney transplantation | STREPTOCOCCUS-PNEUMONIAE | UROLOGY & NEPHROLOGY | ADAMTS13 DEFICIENCY | PEDIATRICS | MEMBRANE COFACTOR PROTEIN | Predictive Value of Tests | Liver Transplantation | Age Factors | Humans | Monitoring, Immunologic | Child, Preschool | Infant | Atypical Hemolytic Uremic Syndrome - immunology | Nephrology - standards | Plasma Exchange | Patient Selection | Atypical Hemolytic Uremic Syndrome - diagnosis | Child | Complement Activation - drug effects | Infant, Newborn | Antibodies, Monoclonal, Humanized - therapeutic use | Atypical Hemolytic Uremic Syndrome - therapy | Risk Factors | Atypical Hemolytic Uremic Syndrome - epidemiology | Cooperative Behavior | Treatment Outcome | Combined Modality Therapy | International Cooperation | Kidney Transplantation | Consensus | Adolescent | Drug Monitoring | Immunologic Factors - therapeutic use | Care and treatment | Hemolytic-uremic syndrome | Research | Life Sciences | Human health and pathology | Plasma | Urologi och njurmedicin | Medical and Health Sciences | Medicin och hälsovetenskap | Pediatrik | Klinisk medicin | Clinical Medicine | Hemolytic | infusion | uremic syndrome | Urology and Nephrology
Journal Article