Results 71 to 80 of about 12,383 (215)
Kimura’s disease with membranoproliferative glomerulonephritis: a case report with literature review
Renal Failure, 2019 Background: Kimura's disease is a rare disease and its etiology is still unclear. Here we reported a case with lymphadenopathy complicated with secondary membranoproliferative glomerulonephritis.
Sensen Su +4 more
doaj +1 more source
Concurrent nephrotic syndrome and acute renal failure caused by chronic lymphocytic leukemia (CLL): a case report and literature review [PDF]
, 2011 Kidney injury associated with lymphocytic leukemia (CLL) is typically caused by direct tumor infiltration which occasionally results in acute renal failure. Glomerular involvement presenting as proteinuria or even nephrotic syndrome is exceptionally rare.
Xianrui Dou +6 more
core +2 more sources
Challenges of modeling pristane‐induced lupus in non‐human primates
Animal Models and Experimental Medicine, Volume 9, Issue 2, Page 399-406, February 2026.Systemic lupus erythematosus (SLE) in cynomolgus monkeys was modeled by two intraperitoneal injections of pristane at a dose of 3.5 mL/kg, administered at weeks 1 and 23. Serum samples from all monkeys that received pristane tested positive for antinuclear antibodies.
Elena Vladimirovna Vinogradova +5 more
wiley +1 more source
Case Reports in Nephrology, 2017 In 2004, the novel category of monoclonal IgG deposition disease has been proposed and termed “proliferative glomerulonephritis with monoclonal IgG deposits” (PGNMID). This disease is characterized by membranoproliferative glomerulonephritis and staining
Homare Shimohata +6 more
doaj +1 more source
T cells, adhesion molecules and modulation of apoptosis in visceral leishmaniasis glomerulonephritis [PDF]
, 2010 Background: Immune complex deposition is the accepted mechanism of pathogenesis of VL glomerulopathy however other immune elements may participate. Further in the present study, no difference was seen between immunoglobulin and C3b deposit intensity in ...
Francisco AL Costa +5 more
core +2 more sources
IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic Purpura
Pediatric Blood &Cancer, Volume 73, Issue 2, February 2026.ABSTRACT Pathogenic variants in IKZF1 (IKAROS) are linked to immunodeficiency, malignancy, and immune dysregulation. We describe a family with a rare IKZF1 variant presenting with humoral immunodeficiency and thrombotic thrombocytopenic purpura (TTP). A non‐consanguineous family was clinically monitored; clinical, immunological, and genetic data (exome
Ilia Spivak +7 more
wiley +1 more source
Journal of Internal Medicine, Volume 299, Issue 2, Page 196-215, February 2026.Abstract Cryoglobulinemia (CG) is defined by the presence of serum immunoglobulins that precipitate below 37°C and redissolve upon rewarming. It is classified into three types based on immunoglobulin composition. Type I, a rare form, involves monoclonal IgM or IgG and is linked to lymphoproliferative disorders.
Anna Linda Zignego +7 more
wiley +1 more source
Immunology and Disease of the Kidney [PDF]
, 1977 The emphasis of this paper is the review of several aspects of renal disease which have immunologic overtones and clinical relevance. The pathogenesis of several subtypes of glomerulonephritis will be discussed, the immunologic implications of ...
Falls, William F., Jr.
core +1 more source
Nephrology, Volume 31, Issue 2, February 2026.This study analysed urinary volatile organic compounds (VOCs) to identify non‐invasive biomarkers for monitoring metabolic mechanisms of SGLT2 inhibitor renoprotection in diabetic kidney disease. The results revealed significantly higher levels of urinary acetone and 2‐pentanone in the treated group, indicating that these ketone‐related VOCs serve as ...
Risa Hara +6 more
wiley +1 more source
On the applicability of the CASPAR criteria in psoriatic arthritis [PDF]
, 2008 Udgivelsesdato: 2008 ...
Junker, P, Pedersen, O B
core +1 more source