Results 11 to 20 of about 27,098 (198)
Membranoproliferative glomerulonephritis complicating Waldenström’s macroglobulinemia [PDF]
Background Lymphoproliferative disorders causing paraproteinemia can be associated with various kidney injuries including the deposition of monoclonal immunoglobulins (Ig).
Kratochvil David +3 more
doaj +3 more sources
Retinal findings in membranoproliferative glomerulonephritis [PDF]
Purpose: To assess the evolution of retinal findings in patients with membranoproliferative glomerulonephritis (MPGN) by funduscopy, intravenous fluorescein angiography and optical coherence tomography. Observations: Three women and one man were followed
Ahmad M. Mansour +6 more
doaj +2 more sources
Membranoproliferative glomerulonephritis in sibs
Idiopathic membranoproliferative glomerulonephritis (MPGN) is a chronic renal disease with variable clinical expression and several distinct morphological subtypes.
O Söylemezoğlu +3 more
doaj +3 more sources
Dermatomyositis Sine Myositis with Membranoproliferative Glomerulonephritis [PDF]
Dermatomyositis (DM) is an autoimmune disease that is characterized by involvement of proximal musculature and skin. We report a 52-year-old woman with a 6-year history of dermatomyositis sine myositis, who developed lower extremity edema and proteinuria.
Mohammad Bagher Owlia +3 more
doaj +2 more sources
Membranoproliferative Glomerulonephritis Associated with Nivolumab Therapy [PDF]
Nivolumab is an immune checkpoint inhibitor that targets programmed death-1 on T cells and is designed to amplify an immunologic reaction against cancer cells.
Jessica Cruz-Whitley +3 more
doaj +2 more sources
Membranoproliferative glomerulonephritis (MPGN) is a rare cause of the nephrotic syndrome in adults and children. Though small focal crescents may be seen in up to 10% of cases of MPGN, the presence of more than 50% crescents (crescentic MPGN) is rare ...
Alok Sharma +4 more
doaj +2 more sources
Background: New classification for membranoproliferative glomerulonephritis has been proposed in the literature. The aim of this study was to compare the clinical, biochemical, etiology and renal biopsy findings of these patients grouped by ...
Cristiane Bitencourt Dias +4 more
doaj +2 more sources
Glomerular Capillary Microaneurysms in Membranoproliferative Glomerulonephritis: A Clinicopathological Study Highlighting the Involvement of IgG3. [PDF]
Glomerular capillary microaneurysms (GCMs) were most frequently observed in proliferative glomerulonephritis with monoclonal immunoglobulin G deposits (PGNMID) among MPGN‐pattern glomerular diseases, but were not restricted to this entity. These lesions were characterized by exclusive IgG3‐dominant glomerular deposition, irrespective of light‐chain ...
Mii A +11 more
europepmc +2 more sources
BACKGROUND: Intronic WT1 mutations are usually causative of Frasier syndrome with focal segmental glomerulosclerosis as the characteristic nephropathy. Membranoproliferative glomerulonephritis is not commonly associated with disorders of sex development ...
Harraway, James +9 more
core +1 more source
Membranoproliferative glomerulonephritis in Russian population [PDF]
Aim. Analysis of etiology, clinical and morphological manifestations, approaches to therapy and prognosis of membranoproliferative glomerulonephritis (MPGN). Materials and methods.
V A Dobronravov, A V Smirnov
doaj +1 more source

