Results 61 to 70 of about 8,451 (217)
An entity‐centric foundation model, GloPath, is introduced for comprehensive glomerular lesion assessment from routine renal biopsy images. Trained on over one million glomeruli, the framework enables robust lesion recognition, grading, and cross modality diag nosis, while uncovering large‐scale clinicopathological associations.
Qiming He +28 more
wiley +1 more source
ABSTRACT Acquired hemophilia A is a rare, potentially life‐threatening bleeding disorder caused by autoantibody inhibitors to coagulation factor VIII. We report the case of an 87‐year‐old female who presented with symptomatic bleeding and was subsequently diagnosed with acquired hemophilia A.
Kevin A. Murgas +4 more
wiley +1 more source
Detection of Antiphospholipid Antibody in Children With Henoch-Schonlein Purpura and Central Nervous System Involvement [PDF]
To explore the mechanisms of central nervous system involvement in children with Henoch-Schonlein purpura, levels of lupus anticoagulant, anticardiolipin antibodies, and anti-beta 2 glycoprotein I antibodies in serum and cerebrospinal fluid were ...
Liu, Ailin, Zhang, Hongwen
core +1 more source
A POSSIBLE RELATIONSHIP BETWEEN SERUM HOMOCYSTEINE LEVEL AND IgA NEPHROPATHY IN CHILDREN
Objective: The evidences from experimental and epidemiological studies suggests that elevated serum homocysteine levels may lead to renal injury and may be a significant risk factor for the development of chronic kidney disease. The aim of this study was
Cemile Pehlivanoğlu +12 more
doaj +1 more source
This graphical abstract depicts the clinical course of a 14‐year‐old male with moderate IgAV‐N treated with telitacicept combined with glucocorticoids as initial therapy. Rapid glucocorticoid tapering, normalized renal function, and continuous remission of proteinuria and hematuria were achieved.
Jiayi Li +7 more
wiley +1 more source
Lupus anticoagulant and thrombosis following Henoch-Schonlein purpura. [PDF]
A male adolescent developed a sinovenous thrombosis 4 weeks following a Henoch-Schonlein purpura episode. A hypercoagulation evaluation revealed a positive lupus anticoagulant.
Spencer, Charles H +2 more
core
The study developed the UPC index by integrating urine red blood cell distribution (URD), urine protein strip, and serum creatinine to enhance the diagnostic accuracy for distinguishing glomerular from nonglomerular hematuria. The UPC index demonstrated superior performance (AUC 0.857) compared to conventional parameters, showing high sensitivity and ...
Hae In Bang +4 more
wiley +1 more source
Recurrent adult onset Henoch-Schonlein Purpura: a case report [PDF]
Henoch-Schonlein purpura is an immunoglobulin A (IgA)-immune complex mediated leukocytoclastic vasculitis that classically manifests with palpable purpura, abdominal pain, arthritis, and hematuria or proteinuria. The condition is much more predominant in
Guido, Bruce +2 more
core +1 more source
Predictive role of laboratory markers and clinical features for recurrent Henoch-Schonlein Purpura in childhood: A study from Turkey [PDF]
Objectives: Henoch Schonlein Purpura is the most common systemic vasculitis of the childhood. the objective of this study was to evaluate whether there is a clinical significance of laboratory parameters and clinical features on the prediction of the ...
Kurugol, Zafer +3 more
core +1 more source
Does clinical exposure to different skin tones during training improve diagnostic ability?
Abstract Background Previous studies have shown that medical students demonstrate poorer performance when diagnosing pathology in skin of colour (SOC) compared to white skin (WS); it is important to understand the reasons underpinning this. If not addressed, poorer differential diagnostic ability in certain skin tones could entrench existing racial ...
Yusra Shammoon +10 more
wiley +1 more source

