Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

J Zuber, F Fakhouri, LT Roumenina, C Loirat… - Nature Reviews …, 2012 - nature.com
In the past decade, a large body of evidence has accumulated in support of the critical role
of dysregulation of the alternative complement pathway in atypical haemolytic uraemic …

Posttransplant recurrence of primary glomerulonephritis

C Ponticelli, RJ Glassock - … Journal of the American Society of …, 2010 - journals.lww.com
All forms of primary GN may recur after kidney transplantation and potentially jeopardize the
survival of the graft. IgA nephritis (IgAN) may recur in approximately one third of patients …

[HTML][HTML] C3 glomerulopathy: consensus report

MC Pickering, VD D'agati, CM Nester, RJ Smith… - Kidney international, 2013 - Elsevier
C3 glomerulopathy is a recently introduced pathological entity whose original definition was
glomerular pathology characterized by C3 accumulation with absent or scanty …

[HTML][HTML] Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

A Servais, LH Noël, LT Roumenina, M Le Quintrec… - Kidney international, 2012 - Elsevier
Dense deposit disease and glomerulonephritis with isolated C3 deposits are
glomerulopathies characterized by deposits of C3 within or along the glomerular basement …

C3 glomerulopathy: clinicopathologic features and predictors of outcome

NR Medjeral-Thomas… - Clinical Journal of the …, 2014 - journals.lww.com
Results Eighty patients with C3 glomerulopathy were identified: 21 with DDD and 59 with
C3GN. Patients with DDD were younger, more likely to have low serum C3 levels, and more …

[图书][B] Heptinstall's Pathology of the Kidney

JC Jennette, VD D'Agati - 2023 - books.google.com
For nearly 60 years, Heptinstall's Pathology of the Kidney has been the reference of choice
for both pathologists and nephrologists for expert, authoritative coverage of kidney disease …

Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome

P Iatropoulos, M Noris, C Mele, R Piras, E Valoti… - Molecular …, 2016 - Elsevier
Background Membranoproliferative glomerulonephritis (MPGN) is an uncommon cause of
chronic nephropathy recently reclassified into immunoglobulin-associated MPGN (Ig-MPGN) …

[HTML][HTML] Evidence-based clinical practice guidelines for nephrotic syndrome 2014

S Nishi, Y Ubara, Y Utsunomiya, K Okada… - Clinical and …, 2016 - Springer
In Japan, original researches on nephrotic syndrome (NS) were initially performed by the
Ministry of Health, Labour and Welfare (MHLW) NS research group. The first definition of NS …

[HTML][HTML] Recurrent glomerulonephritis after kidney transplantation

BY Choy, TM Chan, KN Lai - American journal of transplantation, 2006 - Elsevier
Thirty to fifty percent of kidney transplant recipients have glomerular diseases as the
underlying causes of end-stage renal failure. While recurrence of glomerulonephritis is an …

Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients

SH Nasr, AM Valeri, GB Appel… - Clinical Journal of the …, 2009 - journals.lww.com
Dense Deposit Disease: Clinicopathologic Study of 32 Pediatr... : Clinical Journal of the
American Society of Nephrology Dense Deposit Disease: Clinicopathologic Study of 32 …