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The American Journal of the Medical Sciences, ISSN 0002-9629, 2017, Volume 353, Issue 4, pp. 320 - 328
Journal Article
Kidney International, ISSN 0085-2538, 08/2012, Volume 82, Issue 4, pp. 465 - 473
C3 glomerulonephritis (C3GN) is a recently described disorder that typically results from abnormalities in the alternative pathway (AP) of complement. Here, we... 
C3GN | proteomics | C3 glomerulopathy | MPGN | alternative pathway of complement | C3 glomerulonephritis | MACULAR DEGENERATION | CLASSIFICATION | RISK | PROTEIN 5 | DENSE DEPOSIT DISEASE | ALTERNATIVE PATHWAY | UROLOGY & NEPHROLOGY | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | Complement C3 - analysis | Predictive Value of Tests | Recurrence | Follow-Up Studies | Humans | Middle Aged | Complement System Proteins - immunology | Laser Capture Microdissection | Molecular Sequence Data | Male | Glomerulonephritis, Membranoproliferative - complications | Complement System Proteins - analysis | Young Adult | Time Factors | DNA Mutational Analysis | Mass Spectrometry | Adult | Autoantibodies - analysis | Complement System Proteins - genetics | Female | Complement Pathway, Alternative - genetics | Proteomics - methods | Child | Amino Acid Sequence | Glomerulonephritis, Membranoproliferative - pathology | Genetic Predisposition to Disease | Proteinuria - immunology | Treatment Outcome | Complement C3 Nephritic Factor - analysis | Hematuria - immunology | Kidney Transplantation | Minnesota | Kidney Glomerulus - pathology | Glomerulonephritis, Membranoproliferative - therapy | Glomerulonephritis, Membranoproliferative - genetics | Glomerulonephritis, Membranoproliferative - immunology | Biopsy | Adolescent | Aged | Kidney Glomerulus - immunology | Mutation | Complement Factor H - genetics
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 10/2018, Volume 31, Issue 10, pp. 1165 - 1168
Background: The association of hyperthyroidism with renal disease is very rare and the importance of timely clinical recognition cannot be overemphasized. Case... 
Graves’ disease | membranoproliferative glomerulonephritis | proteinuria | Graves' disease | PEDIATRICS | THYROIDITIS | ENDOCRINOLOGY & METABOLISM | Female | Graves Disease - complications | Glomerulonephritis, Membranoproliferative - complications | Child | Humans | Vasculitis, Leukocytoclastic, Cutaneous - complications
Journal Article
Clinical Journal of the American Society of Nephrology, ISSN 1555-9041, 01/2014, Volume 9, Issue 1, pp. 46 - 53
Journal Article
Journal of the American Society of Nephrology : JASN, ISSN 1046-6673, 2014, Volume 25, Issue 4, pp. 850 - 863
Journal Article
Retinal Cases and Brief Reports, ISSN 1935-1089, 01/2016, Volume 10, Issue 1, pp. 72 - 78
Membranoproliferative glomerulonephritis (MPGN) classification has been changed from purely anatomic to molecular. This report describes two cases of MPGN with... 
Glomerulonephritis | Genetics | Complement factor H | Complement | Drusen | Retinal Drusen - etiology | Humans | Subretinal Fluid | Adult | Female | Glomerulonephritis, Membranoproliferative - complications | Fundus Oculi
Journal Article
Journal Article
by Zaidan, Mohamad and Terrier, Benjamin and Pozdzik, Agnieszka and Frouget, Thierry and Rioux-Leclercq, Nathalie and Combe, Christian and Lepreux, Sébastien and Hummel, Aurélie and Noël, Laure-Hélène and Marie, Isabelle and Legallicier, Bruno and François, Arnaud and Huart, Antoine and Launay, David and Kaplanski, Gilles and Bridoux, Frank and Vanhille, Philippe and Makdassi, Raifah and Augusto, Jean-François and Rouvier, Philippe and Karras, Alexandre and Jouanneau, Chantal and Verpont, Marie-Christine and Callard, Patrice and Carrat, Fabrice and Hermine, Olivier and Léger, Jean-Marc and Mariette, Xavier and Senet, Patricia and Saadoun, David and Ronco, Pierre and Brochériou, Isabelle and Cacoub, Patrice and Plaisier, Emmanuelle and Aaron, Laurent and Abad, Sébastien and Bakir, Redouane and Belenotti, Pauline and Benarous, Lucas and Beneton, Nathalie and Blaison, Gilles and Blanchard-Delaunay, Claire and Bonnet, Fabrice and Cathébras, Pascal and Carrat, Fabrice and Chiche, Laurent and Chosidow, Olivier and Combe, Bernard and Cordonnier, Carole and Costedoat-Chalumeau, Nathalie and Cougoul, Pierre and Cribier, Bernard and Croue, Anne and Daniel, Laurent and Defuentes, Gilles and Desvaux, Dominique and Dijoud, Frédérique and Diot, Elisabeth and Doucet, Laurent and Duong Van Huyen, Jean-Paul and Durieu, Isabelle and Evon, Philippe and Felix, Sophie and Ferlicot, Sophie and Fraisse, Thibault and Francès, Camille and Francois, Hélène and Geffray, Loik and Gil, Helder and Goujon, Jean Michel and Guillaudeau, Angélique and Gutnecht, Jean and Hachulla, Eric and Hinschberger, Olivier and Hot, Arnaud and Jourde, Noémie and Kahn, Jean-Emmanuel and Kemmeny, Jean Louis and Lacraz, Adeline and Lambotte, Olivier and Larroche, Claire and Lazaro, Estibaliz and Le Guenno, Guillaume and Leblond, Véronique and Limal, Nicolas and Liozon, Eric and Lok, Catherine and Loustaud-Ratti, Véronique and Ly, Kim and Machet, Marie-Christine and Maillard, Hervé and Martin, Antoine and Matignon, Marie and Meyer, Olivier and Michel, Catherine and Modesto-Segonds, Anne and Modiano, Philippe and Nochy, Dominique and Noel, David and Nove-Josserand, Raphaele and ... and CryoVas Study Grp and CryoVas study group and the CryoVas study group
Journal of the American Society of Nephrology, ISSN 1046-6673, 2016, Volume 27, Issue 4, pp. 1213 - 1224
Journal Article
Journal Article
Internal Medicine, ISSN 0918-2918, 2009, Volume 48, Issue 3, pp. 157 - 162
Autoimmune pancreatitis is characterized by diffuse enlargement of the pancreas, irregular narrowing of the pancreatic duct, high serum levels of IgG4, and... 
membranoproliferative glomerulonephritis-like glomerular disease | idiopathic thrombocytopenic purpura | IgG4 | autoimmune pancreatitis | tubulointerstitial nephritis | Idiopathic thrombocytopenic purpura | Glomerulonephritis-like glomerular disease | Membranoproliferative | Autoimmune pancreatitis | Tubulointerstitial nephritis | SYSTEMIC-DISEASE | INVOLVEMENT | INTERSTITIAL PNEUMONIA | SJOGRENS-SYNDROME | MIKULICZS-DISEASE | INFILTRATION | MEDICINE, GENERAL & INTERNAL | RETROPERITONEAL FIBROSIS | CHOLANGITIS | SCLEROSING PANCREATITIS | RENAL LESIONS | Glomerulonephritis, Membranoproliferative - pathology | Heart Failure - complications | Purpura, Thrombocytopenic, Idiopathic - complications | Nephritis, Interstitial - complications | Nephritis, Interstitial - diagnosis | Humans | Immunoglobulin G | Autoimmune Diseases - complications | Male | Glomerulonephritis, Membranoproliferative - complications | Pancreatitis - complications | Pancreatitis - drug therapy | Purpura, Thrombocytopenic, Idiopathic - drug therapy | Nephritis, Interstitial - pathology | Fatal Outcome | Aged, 80 and over | Anti-Inflammatory Agents - therapeutic use | Pancreatitis - immunology | Pneumonia, Mycoplasma - complications | Glomerulonephritis, Membranoproliferative - diagnosis | Prednisolone - therapeutic use | Autoimmune Diseases - drug therapy
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 2009, Volume 24, Issue 11, pp. 2097 - 2108
Renal transplantation (Tx) is the treatment of choice for end-stage renal disease. The incidence of acute rejection after renal Tx has decreased because of... 
Haemolytic uraemic syndrome | Disease recurrence | Focal and segmental glomerulosclerosis | Systemic lupus erythematosus | Membranoproliferative glomerulonephritis | Renal transplantation | Child | Primary hyperoxaluria type 1 | RITUXIMAB TREATMENT | HEMOLYTIC-UREMIC SYNDROME | FOCAL-SEGMENTAL GLOMERULOSCLEROSIS | I MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | POSTERIOR URETHRAL VALVES | PRIMARY HYPEROXALURIA TYPE-1 | THROMBOTIC MICROANGIOPATHY | KIDNEY-TRANSPLANTATION | UROLOGY & NEPHROLOGY | IGA NEPHROPATHY | PEDIATRICS | NEPHROTIC SYNDROME | Recurrence | Hemolytic-Uremic Syndrome - etiology | Glomerulosclerosis, Focal Segmental - surgery | Hyperoxaluria, Primary - complications | Hyperoxaluria, Primary - etiology | Humans | Child, Preschool | Glomerulonephritis, Membranoproliferative - complications | Glomerulosclerosis, Focal Segmental - complications | Incidence | Glomerulosclerosis, Focal Segmental - etiology | Hemolytic-Uremic Syndrome - surgery | Kidney Diseases - epidemiology | Lupus Erythematosus, Systemic | Kidney Diseases - complications | Glomerulonephritis - etiology | Glomerulonephritis, Membranous - etiology | Glomerulonephritis - epidemiology | Hyperoxaluria, Primary - surgery | Kidney - surgery | Glomerulonephritis, Membranous - surgery | Hemolytic-Uremic Syndrome - complications | Risk Factors | Glomerulonephritis, Membranoproliferative - surgery | Glomerulonephritis - surgery | Graft Rejection - surgery | Glomerulonephritis, Membranous - complications | Kidney Diseases - etiology | Glomerulonephritis, Membranoproliferative - etiology | Kidney Transplantation - adverse effects | Complications and side effects | Care and treatment | Kidneys | Chronic kidney failure | Patient outcomes | Development and progression | Transplantation | Research | Health aspects | Review | Primary hyperoxaluria type 1
Journal Article