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Seminars in Immunopathology, ISSN 1863-2297, 1/2018, Volume 40, Issue 1, pp. 49 - 64
Atypical hemolytic uremic syndrome (aHUS), C3 glomerulopathy (C3G), and paroxysmal nocturnal hemoglobinuria (PNH) are prototypical disorders of complement... 
Internal Medicine | Complement | Biomedicine | Immunology | PNH | C3G, aHUS | HEMOLYTIC-UREMIC SYNDROME | ISOLATED C3 DEPOSITS | PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA | PROSPECTIVE CLINICAL-TRIAL | NEPHRITIC FACTOR C3NEF | FACTOR-I | IMMUNOLOGY | PATHOLOGY | IDIOPATHIC MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | FACTOR-H-AUTOANTIBODIES | DENSE DEPOSIT DISEASE | MEMBRANE COFACTOR PROTEIN | Genetic Predisposition to Disease | Atypical Hemolytic Uremic Syndrome - therapy | Hemoglobinuria, Paroxysmal - metabolism | Complement C3 - metabolism | Humans | Complement System Proteins - immunology | Atypical Hemolytic Uremic Syndrome - etiology | Hemoglobinuria, Paroxysmal - etiology | Complement Activation - immunology | Glomerulonephritis - metabolism | Molecular Targeted Therapy | Complement C3 - immunology | Complement System Proteins - metabolism | Complement Activation - genetics | Phenotype | Animals | Disease Susceptibility - immunology | Atypical Hemolytic Uremic Syndrome - metabolism | Glomerulonephritis - pathology | Complement System Proteins - genetics | Atypical Hemolytic Uremic Syndrome - diagnosis | Glomerulonephritis - etiology | Hemoglobinuria, Paroxysmal - therapy | Hemoglobinuria, Paroxysmal - diagnosis | Gene mutations | Hemolytic uremic syndrome | Developmental stages | Complement component C3 | Paroxysmal nocturnal hemoglobinuria | Mutation | Alternative pathway | Cell surface | Review
Journal Article
Clinical Journal of the American Society of Nephrology, ISSN 1555-9041, 2017, Volume 12, Issue 8, pp. 1237 - 1247
Background Pregnancy is associated with various forms of thrombotic microangiopathy, including hemolytic uremic syndrome. A previous small French study... 
COFACTOR PROTEIN CD46 | C3 | 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, 12/2015, Volume 88, Issue 6, pp. 1314 - 1322
Abnormal regulation of the complement alternative pathway is associated with C3 glomerulopathy. Complement factor H is the main plasma regulator of the... 
therapeutic | mini-FH | factor H | C3 glomerulopathy | Therapeutic | Factor H | Mini-FH | CELLS | ACTIVATION | HEMOLYTIC-UREMIC SYNDROME | PROTEIN | NEISSERIA-MENINGITIDIS | SURFACE-RECOGNITION | DENSE DEPOSIT DISEASE | ALTERNATIVE PATHWAY | UROLOGY & NEPHROLOGY | DECAY-ACCELERATING FACTOR | BINDING | Basic Research
Journal Article
Kidney International, ISSN 0085-2538, 11/2017, Volume 92, Issue 5, pp. 1261 - 1271
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 11/2014, Volume 25, Issue 11, pp. 2425 - 2433
Journal Article