Results 101 to 110 of about 12,383 (215)

Diagnostic and therapeutic challenges in dense deposit disease: case report

Počki
We report a complex case of a 15-year-old girl initially diagnosed with post-streptococcal glomerulonephritis (PSGN) but later identified as having dense deposit disease, which was initially classified as type 2 membranoproliferative glomerulonephritis ...
Anand Prasad, Dhruv Jain, Navya Jaiswal, Harsha Shahi   +3 more
doaj   +1 more source

C3 glomerulonephritis associated with monoclonal gammopathy of renal significance: case report

BMC Nephrology, 2018
Background Morbidity associated with monoclonal gammopathy of renal significance is high due to the severe renal lesions and the associated systemic alterations.
Juana Alonso-Titos, Lara Perea-Ortega, Eugenia Sola, Alvaro Torres-Rueda, Myriam León, Remedios Toledo, Ana D. Duarte, Teresa Vazquez, Maria Dolores Martinez-Esteban, Alicia Bailen, Pedro Ruiz-Esteban, Domingo Hernandez   +11 more
doaj   +1 more source

Efficacy and Safety of Pegcetacoplan in Kidney Transplant Recipients With Recurrent Complement 3 Glomerulopathy or Primary Immune Complex Membranoproliferative Glomerulonephritis. [PDF]

Kidney Int Rep
Bomback AS, Daina E, Remuzzi G, Kanellis J, Kavanagh D, Pickering MC, Sunder-Plassmann G, Walker PD, Wang Z, Ahmad Z, Fakhouri F.   +10 more
europepmc   +2 more sources

Haemolytic uraemic syndrome caused by factor H mutation: is single kidney transplantation under intensive plasmatherapy an option? [PDF]

, 2017
Complement factor H (CFH) mutation is one of the causes of atypical haemolytic uraemic syndrome (aHUS). Patients with CFH mutation-associated aHUS progress often to end-stage renal disease despite plasma exchange therapy.
Dickenmann, Michael, Frémeaux-Bacchi, Véronique, Hirt-Minkowski, Patricia, Mayr, Michael, Schaub, Stefan, Schifferli, Jürg A., Steiger, Jürg   +6 more
core  

Tacrolimus in pediatric renal transplantation [PDF]

, 1996
Tacrolimus was used as the primary immunosuppressive agent in 69 pediatric renal transplantations between December 17, 1989, and June 30, 1995. Children undergoing concomitant or prior liver and/or intestinal transplantation were excluded from analysis ...
Ellis, D, Fung, JJ, Gilboa, N, Gritsch, HA, Hakala, TR, Irish, W, Jordan, ML, Lombardozzi-Lane, S, Scantlebury, VP, Shapiro, R, Simmons, RL, Starzl, TE, Vivas, C   +12 more
core   +1 more source

Profile of glomerular diseases associated with hepatitis B and C: A single-center experience from India

Saudi Journal of Kidney Diseases and Transplantation, 2017
Hepatitis B and C are known to affect kidneys in a number of ways. Glomerular diseases associated with hepatitis B and C include membranous nephropathy (MN), membranoproliferative glomerulonephritis (MPGN), focal segmental glomerulosclerosis ...
Nishad Raveendran, Pankaj Beniwal, Amith Vijay Leon D′Souza, Rajendra Singh Tanwar, Piyush Kimmatkar, Dhananjai Agarwal, Vinay Malhotra   +6 more
doaj   +1 more source

ACUTE RENAL FAILURE DUE TO MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS AND TUMORAL CELL INFILTRATION IN A PATIENT WITH MANTLE CELL LYMPHOMA: A CASE REPORT

Mediterranean Journal of Hematology and Infectious Diseases, 2014
Mantle cell lymphoma (MCL) is a subtype of non-Hodgkin lymphoma that presents in a disseminated state at diagnosis. Multiple extranodal site involvement is frequent, however genitourinary system is rarely affected, being kidneys the most common location.
Maria Julia Montoro, Elias Alejandro Jatem, Pau Abrisqueta, Nerea Castillo, Maria Teresa Salcedo, Josepa Vila   +5 more
doaj  

Histopathological findings in elderly patients [PDF]

, 2010
INTRODUCTION: The elderly population has significantly increased worldwide and recent studies have evidenced a 10-year increase in Brazilian life expectancy.
Bastos, Marcus Gomes, Carmo, Priscylla Aparecida Vieira do, Carmo, Wander Barros do, Franco, Marcello Fabiano de [UNIFESP], Mastroianni Kirsztajn, Gianna [UNIFESP]   +4 more
core   +2 more sources

Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in mice [PDF]

, 2019
Atypical hemolytic uremic syndrome (aHUS) is frequently associated in humans with loss-of-function mutations in complement-regulating proteins or gain-of-function mutations in complement-activating proteins.
Atkinson, John P, Barlow, Paul N, Cook, H. T, Cooke, Katie, Denton, Harriet, Kavanagh, David, Liszewski, M. K, Marchbank, Kevin J, Pappworth, Isabel Y, Pickering, Matthew C, Smith-Jackson, Kate, Yang, Yi   +11 more
core   +3 more sources

Chidhood Nephrotic Syndrome in Ilorin.

Nigerian Journal of Paediatrics
Summary: A cohort of 17 children (12M:5F), aged 3-16 years, with nephrotic syndrome seen at the University of Ilorin Teaching Hospital, Ilorin, between Janu ary 1995 and December 1998 were studied. Renal biopsies were performed in eight patients.
Adedoyin OT , Gbelee HOD , Adeniyi A.   +2 more
doaj