Results 141 to 150 of about 8,337 (255)
Biomarkers of Lupus Nephritis Histopathology: Where Do We Stand?
Objective Lupus nephritis (LN) is characterized by a variable disease course, necessitating continuous monitoring. There is an urgent need to identify noninvasive biomarkers. By reviewing and critically assessing the quality of existing studies on LN biomarkers correlating with histopathology, we here explore the challenges in promoting their use in ...
Valentina Querin +11 more
wiley +1 more source
Not So Benign: Revisiting Pure Membranous Lupus Nephritis. [PDF]
Uzzo M, Calatroni M, Moroni GL.
europepmc +1 more source
Association of Autoimmune Diseases With Pancreatic Cancer: A Nationwide Follow‐Up Study From Sweden
Graphic abstract illustrating the nationwide cohort design used to investigate the association between autoimmune diseases and the risk of pancreatic cancer in Sweden. ABSTRACT Background The incidence of pancreatic cancer (PC) and autoimmune diseases (ADs) has been increasing worldwide.
Jiarong Gu +6 more
wiley +1 more source
At AML initial diagnosis, the lysozyme and creatinine levels were positively correlated. However, the effect of lysozyme levels on AML prognosis is limited, because renal function recovers in many patients with high‐lysozyme levels after chemotherapy. ABSTRACT Lysozyme‐induced nephropathy is a complication of chronic myelomonocytic leukemia and acute ...
Takafumi Tsushima +8 more
wiley +1 more source
Alport Syndrome: A Specific Case of Hereditary Nephropathy
Cohan Eric
doaj
Acute pancreatitis as a complication of epstein-barr virus infection: A case report and narrative review. [PDF]
Zako J, Cornut G, Monière-Wollank A.
europepmc +1 more source
Pediatric Non‐Lupus Full House Nephropathy: Case Report and Review of Literature
ABSTRACT Lupus nephritis is a severe manifestation of systemic lupus erythematosus (SLE) typically characterized by glomerular “full‐house” immunofluorescence. However, non‐lupus nephropathies may occasionally exhibit similar patterns, creating diagnostic uncertainty.
Mohammad Firoz Anjum +4 more
wiley +1 more source
Coexistence of Alport Syndrome and Fabry Disease in a Female with R112H Variant: Early Progression of Fabry Nephropathy. [PDF]
Grimaldi A +10 more
europepmc +1 more source
SQDHD exerts neuroprotective effects and alleviates behavioral deficits in PIL mice, likely by inhibiting the JAK1‐STAT3 pathway in activated CVECs. These findings underscore the therapeutic potential of SQDHD and establish it as a promising candidate for the treatment of NPSLE.
Jie Chen +9 more
wiley +1 more source

