Results 101 to 110 of about 18,807 (198)
Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation [PDF]
, 2011 Complement factor H (CFH) is a regulator of the alternative complement activation pathway. Mutations in the CFH gene are associated with atypical hemolytic uremic syndrome, membranoproliferative glomerulonephritis type II and C3 glomerulonephritis. Here,
Marquart, H V +13 more
core +1 more source
C3 metabolism in acute glomerulonephritis: Implications for sites of complement activation [PDF]
, 1984 C3 metabolism in acute glomerulonephritis: Implications for sites of complement activation. Immunochemical and metabolic studies of complement were performed in 11 patients with acute poststreptococcal glomerulonephritis (AGN) to determine the mechanism ...
Pussell, Bruce A. +4 more
core +1 more source
Indian Journal of Kidney DiseasesImmunotactoid glomerulonephritis (ITGN) is characterized by organized deposits in the form of microtubules on electron microscopy that stain for monoclonal or polyclonal immunoglobulins (Igs) along with complements.
Gnanapriya Vellaisamy +4 more
doaj +1 more source
C3-Dominant Infection Related Crescentic Glomerulonephritis.
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologiaInfection related glomerulonephritis and more specifically streptococcal glomerulonephritis is a rare disease in adults, and so is C3 glomerulonephritis. It has been recognized that a clinical and morphological overlap between these two entities exists. We present a case of a 59-year-old man with previous treated HIV infection with virological response,
Wilson, Suarez Molina +8 more
openaire +2 more sources
Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies [PDF]
, 2012 Dense deposit disease and glomerulonephritis with isolated C3 deposits are glomerulopathies characterized by deposits of C3 within or along the glomerular basement membrane.
Le Quintrec, Moglie +14 more
core +1 more source
Kidney Research and Clinical Practice, 2014 Background: All types of membranoproliferative glomerulonephritis (MPGN) are progressive diseases with poor prognoses. Recently, a newly proposed classification of these diseases separated them into immune complex- and complement-mediated diseases.
Sung Ae Woo +9 more
doaj +1 more source
C3 glomerulopathia és új célzott kezelési lehetősége = C3 glomerulopathy and its new targeted treatment options [PDF]
A membranoproliferatív glomerulonephritisek szövettani alapúfelosztása helyett az utóbbi években az etiológiai alapú osztályozás kezd elterjedni.A komplementrendszerben a C3 aktiválódásának zavara következtében kialakulóglomerularis betegségeket ...
Kovács, Tibor
core +1 more source
C3 glomerulopathy disease [PDF]
, 2018 C3 glomerulopati (C3G), kompleman aktivasyonunun anormal kontrolü ile oluşan bir grup böbrek hastalığını kapsayan yakın zamanda tanımlanmış bir hastalıktır.
Ferhan Candan³ +2 more
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Rituximab for Treatment of Membranoproliferative Glomerulonephritis and C3 Glomerulopathies [PDF]
, 2020 Membranoproliferative glomerulonephritis (MPGN) is a histological pattern of injury resulting from predominantly subendothelial and mesangial deposition of immunoglobulins or complement factors with subsequent inflammation and proliferation particularly ...
Michael Rudnicki
core
A rare co-existence of celiac disease and C3 glomerulopathy
Nefrología (English Edition)Glomerulonephritis associated with celiac disease (CD) is rarely reported. Here we report a rare case of nephrotic syndrome associated with C3 glomerulopathy (C3G) in a patient with CD. A 19-year-old female with bilateral leg swelling and hypoalbuminemia
Ali Ilter +3 more
doaj +1 more source