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by Rovin, Brad H and Caster, Dawn J and Cattran, Daniel C and Gibson, Keisha L and Hogan, Jonathan J and Moeller, Marcus J and Roccatello, Dario and Cheung, Michael and Wheeler, David C and Winkelmayer, Wolfgang C and Floege, Jürgen and Adler, Sharon G and Alpers, Charles E and Ayoub, Isabelle and Bagga, Arvind and Barbour, Sean J and Barratt, Jonathan and Chan, Daniel T.M and Chang, Anthony and Choo, Jason Chon Jun and Cook, H. Terence and Coppo, Rosanna and Fervenza, Fernando C and Fogo, Agnes B and Fox, Jonathan G and Glassock, Richard J and Harris, David and Hodson, Elisabeth M and Hoxha, Elion and Iseki, Kunitoshi and Jennette, J. Charles and Jha, Vivekanand and Johnson, David W and Kaname, Shinya and Katafuchi, Ritsuko and Kitching, A. Richard and Lafayette, Richard A and Li, Philip K.T and Liew, Adrian and Lv, Jicheng and Malvar, Ana and Maruyama, Shoichi and Mejía-Vilet, Juan Manuel and Mok, Chi Chiu and Nachman, Patrick H and Nester, Carla M and Noiri, Eisei and O'Shaughnessy, Michelle M and Özen, Seza and Parikh, Samir M and Park, Hyeong-Cheon and Peh, Chen Au and Pendergraft, William F and Pickering, Matthew C and Pillebout, Evangéline and Radhakrishnan, Jai and Rathi, Manish and Ronco, Pierre and Smoyer, William E and Tang, Sydney C.W and Tesař, Vladimír and Thurman, Joshua M and Trimarchi, Hernán and Vivarelli, Marina and Walters, Giles D and Wang, Angela Yee-Moon and Wenderfer, Scott E and Wetzels, Jack F.M and Conf Participants and Conference Participants
Kidney International, ISSN 0085-2538, 02/2019, Volume 95, Issue 2, pp. 281 - 295
In November 2017, the Kidney Disease: Improving Global Outcomes (KDIGO) initiative brought a diverse panel of experts in glomerular diseases together to... 
monoclonal gammopathies of renal significance | membranoproliferative glomerulonephritis | C3 glomerulopathy | KDIGO | lupus nephritis | anti-neutrophil cytoplasmic antibody–associated vasculitis | minimal change disease | focal and segmental glomerulosclerosis | CLINICS CLASSIFICATION CRITERIA | SYSTEMIC-LUPUS-ERYTHEMATOSUS | HEMOLYTIC-UREMIC SYNDROME | THROMBOTIC MICROANGIOPATHY | UROLOGY & NEPHROLOGY | ANCA-ASSOCIATED VASCULITIS | anti-neutrophil cytoplasmic antibody-associated vasculitis | IDIOPATHIC NEPHROTIC SYNDROME | B MEMBER 9 | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | CHAIN DEPOSITION DISEASE | STAGE RENAL-DISEASE | Glomerulonephritis - therapy | Genetic Testing | Humans | Paraproteinemias - genetics | Nephrology - standards | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis - diagnosis | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis - complications | Nephrology - methods | Glomerulonephritis - etiology | Nephrosis, Lipoid - etiology | Glomerular Filtration Rate | Paraproteinemias - diagnosis | Risk Factors | Biomarkers - analysis | Treatment Outcome | Nephrosis, Lipoid - therapy | Paraproteinemias - complications | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis - genetics | Podocytes - pathology | Consensus Development Conferences as Topic | Disease Progression | Nephrosis, Lipoid - pathology | Glomerulonephritis - pathology | Podocytes - immunology | Practice Guidelines as Topic | Life Sciences | Biochemistry, Molecular Biology | Genomics
Journal Article
Kidney International, ISSN 0085-2538, 02/2019, Volume 95, Issue 2, pp. 268 - 280
Journal Article
NEFROLOGÍA, ISSN 0211-6995, 07/2016, Volume 36, Issue 4, pp. 339 - 346
La lesión renal aguda en los pacientes críticos representa un factor de riesgo independiente de la morbilidad y la mortalidad a corto y a largo plazo, con un... 
Biomarkers | Biomarcadores | Lesión renal aguda | Acute kidney injury
Journal Article
NEFROLOGIA (English Edition), ISSN 2013-2514, 07/2016, Volume 36, Issue 4, pp. 339 - 346
Acute kidney injury in the critically ill represents an independent risk factor of morbidity and mortality in the short and long terms, with significant... 
Biomarkers | Biomarcadores | Lesión renal aguda | Acute kidney injury
Journal Article
Salud(i)Ciencia, ISSN 1667-8982, 11/2012, Volume 19, Issue 5, pp. 427 - 430
Journal Article
Journal of Nephrology, ISSN 1121-8428, 12/2016, Volume 29, Issue 6, pp. 791 - 797
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 05/2015, Volume 30, Issue suppl_3, pp. iii437 - iii437
Journal Article
International Journal of Nephrology, ISSN 2090-214X, 2017, Volume 2017, pp. 1287289 - 7
. Despite enzyme replacement therapy, Fabry nephropathy still progresses. Podocyturia is an irreversible event that antedates proteinuria and leads to chronic... 
Medicine, Experimental | Medical research | Enzymes | Lipids | Chronic kidney failure | Urine | Mutation | Kidney diseases | Laboratories | Patients
Journal Article
Nephron Extra, ISSN 1664-5529, 05/2017, Volume 7, Issue 2, pp. 52 - 61
Podocyturia may determine the evolution to podocytopenia, glomerulosclerosis, and renal failure. According to the Oxford classification of IgA nephropathy... 
Glomerulonephritis | Glomerulosclerosis | IgA nephropathy | Podocyturia | CD80 | Urokinase-type plasminogen activator receptor | Integrins | Proteinuria
Journal Article
Clinical kidney journal, ISSN 2048-8505, 02/2019, Volume 12, Issue 1, pp. 53 - 60
In Fabry nephropathy, podocyturia is an early event that may lead to glomerulosclerosis and chronic kidney disease. The glycocalyx is a potential podocyte... 
Journal Article
Journal Article
Nephron Clinical Practice, ISSN 1660-2110, 02/2011, Volume 117, Issue 3, pp. c198 - c205
Journal Article