Results 51 to 60 of about 21,381 (225)
Incidence of glomerulonephritis in the western part of Switzerland over the last decade
Swiss Medical Weekly, 2020 BACKGROUND Glomerulonephritis is a rare yet serious group of diseases with a high risk of progression to end-stage renal disease. For optimal healthcare planning, detailed epidemiological and demographic data are essential.
Giliane Nanchen +6 more
doaj +1 more source
Clinical implications of imlifidase interference in antibody screening and transfusion management
Transfusion, EarlyView.Abstract Background Imlifidase has received conditional approval from the EMA for desensitizing deceased donor kidney transplant recipients. It works by cleaving IgG into F(ab′)2 and Fc fragments, thereby reducing the risk of antibody‐mediated rejection. However, its impact on diagnostic assays remains understudied. Case Report We present the case of a
Zgjim Osmani +2 more
wiley +1 more source
IGA Nephropathy : From Molecules to Men / [PDF]
, 1999 The author of this volume has studied IgA nephropathy for nearly 25 years, almost as long as primary IgA nephropathy has been recognized as a new disease.
Tomino, Y.
core
Experimental Physiology, EarlyView.Abstract IgA nephropathy (IgAN) is a common type of primary glomerulonephritis in children. The pathogenesis of childhood IgAN remains unclear, and there is a lack of effective non‐invasive biomarkers for this disease. Single‐cell RNA sequencing was performed in children with IgAN to delineate cellular and molecular compositions, and subcluster ...
Ling Yu +7 more
wiley +1 more source
Thrombinuria and fibrin deposition in glomerular tissues in glomerulonephritis. [PDF]
, 2015 *Thr and Fib indicate thrombinuria and fibrin deposition, respectively. Fibrin deposition was determined via immunofluorescence microscopy, and thrombin activities > and below the detection limit (0.2 U/L) were regarded as positive (+) and negative ...
Takahisa Imamura (692666) +6 more
core +1 more source
The FASEB Journal, Volume 40, Issue 13, 15 July 2026.Active immunization with recombinant THSD7A in mice induces autoreactive B cell activation and differentiation into CD138+ antibody‐secreting cells, leading to the production of anti‐THSD7A autoantibodies, glomerular immune injury and proteinuria, characteristic of membranous nephropathy. NDP‐MSH treatment modulates the MITF/IRF4 axis in primed B cells,
Mingzhuo Zhang +4 more
wiley +1 more source
Acute poststreptococcal glomerulonephritis superimposed on IgA nephropathy [PDF]
, 2008 Superimposition of poststreptococcal glomerulonephritis (PSGN) on the course of IgA nephropathy (IgAN) is uncommon. A case of PSGN during IgA nephropathy is presented.
임범진
core
Cutaneous IgA Vasculitis in Primary Sjögren Disease: Findings From a Medical Record–Based Review
ACR Open Rheumatology, Volume 8, Issue 7, July 2026.Objective This study aimed to describe clinical observations of patients presenting with palpable purpura, which is suspected to represent IgA vasculitis (IgAV) based on direct immunofluorescence (DIF), who were ultimately diagnosed with cutaneous vasculitis associated with primary Sjögren disease (SjD).
Shay Brikman +2 more
wiley +1 more source
BMC NephrologyBackground The factors influencing diffuse crescentic glomerulonephritis renal survival and prognosis remain uncertain. Additionally, there’s no literature on the clinical outcomes of IgA nephropathy, lupus nephritis, and IgA vasculitis nephritis in type
Shan Wen +5 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT A 66‐year‐old man presented with dialysis‐dependent acute kidney injury without cytopenia or peripheral blasts. Kidney biopsy revealed leukemic infiltration and led to the diagnosis of Philadelphia chromosome‐negative B‐acute lymphoblastic leukemia.
Semin Cho +9 more
wiley +1 more source