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Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Papillorenal syndrome (PAPRS), or renal coloboma syndrome, is a rare autosomal dominant disorder caused by PAX2 mutations. It classically manifests with renal hypodysplasia and optic nerve anomalies. However, recent literature suggests an expanding phenotypic spectrum.
Nadira Sultana +2 more
wiley +1 more source
Mesangial cell-binding activity of serum immunoglobulin G in patients with lupus nephritis [PDF]
, 2014 In vitro data showed that immunoglobulin G (IgG) from patients with lupus nephritis (LN) could bind to cultured human mesangial cells (HMC). The clinical relevance of such binding was unknown.
Chan, DTM +4 more
core +1 more source
Use of Plasmapheresis and Immunosuppressants to Treat Diffuse Alveolar Hemorrhage in a Patient with Granulomatosis with Polyangiitis. [PDF]
, 2019 Granulomatosis with polyangiitis (GPA) is a systemic granulomatous inflammatory disease characterized by small-to-medium vessel vasculitis due to Central Anti-Neutrophil Cytoplasmic Antibody (C-ANCA).
Sattar, Yasar +4 more
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Immunohistochemistry in the diagnosis of membranous glomerulonephritis: a comparative study of chromogen + counterstaining combination [PDF]
, 2013 A glomerulonefrite membranosa faz parte das doenças glomerulares que provocam glomerulonefrite crônica, apresentando-se como uma das causas da doença renal terminal.
Dias, Susana C. +3 more
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C3 deposits worsens the prognosis in type iii extracapillary glomerulonephritis
Nefrología (English Edition), 2018 Introduction: Type iii extracapillary glomerulonephritis (PEGN) is a common cause of rapidly progressive glomerulonephritis and it is usually associated with circulating anti-neutrophil cytoplasmic antibodies (ANCAs). Recent evidence points to complement
Marina Sánchez-Agesta Martínez +6 more
doaj +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
Hepatitis B and Renal Disease [PDF]
, 2010 Glomerulonephritis is an important extrahepatic manifestation of chronic hepatitis B virus (HBV) infection. The uncommon occurrence, variability in renal histopathology, and heterogeneity in clinical course present challenges in clinical studies and have
Tak Mao Chan
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22nd Annual Scientific Meeting of the Australasian Society of Nephrology [PDF]
, 1986 This repository item contains a single issue of The ISCIP Analyst, an analytical review journal published from 1996 to 2010 by the Boston University Institute for the Study of Conflict, Ideology, and ...
Cavan, Susan +8 more
core +20 more sources
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
Alternative Pathway Dysregulation and the Conundrum of Complement Activation by IgG4 Immune Complexes in Membranous Nephropathy [PDF]
, 2016 Membranous nephropathy (MN), a major cause of nephrotic syndrome, is a non-inflammatory immune kidney disease mediated by IgG antibodies that form glomerular subepithelial immune complexes.
Dorin-Bogdan Borza
core +2 more sources