Results 51 to 60 of about 27,754 (168)
Could it be Henoch-Schönlein purpura?
Background: Henoch-Schönlein purpura is the most common form of systemic vasculitis in the paediatric setting with 90% of cases occuring in childhood.
Cheng, Lisa N C +2 more
core +1 more source
Recurrent Henoch-Schönlein purpura controlled with ciclosporin
Even when Henoch–Schönlein purpura is not accompanied by nephritis, powerful immunosuppressive therapy may be ...
Harries, M.J.; id_orcid +2 more
core +1 more source
Henoch-Schönlein purpura nephritis and IgA nephropathy are currently considered to be different clinical presentations of the same disease. There is need for a reliable proven, morphologic classification that can help clinicians more accurately formulate
Hamid Nasri
doaj
PECU: A multicenter study on pediatric patients with cold‐induced urticaria
Abstract Background Cold‐induced urticaria (ColdU) is a rare chronic inducible urticaria that can cause systemic reactions, including cold‐induced anaphylaxis (ColdA), but pediatric data are limited. The aim of this study was to evaluate the clinical characteristics, comorbidities, management approaches, risk of anaphylaxis, and long‐term course of ...
Betul Gemici Karaaslan +59 more
wiley +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
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
Henoch-Schonlein Purpura (HSP)
—Henoch-Schonlein purpura (HSP) is a systemic vasculitic disease (vascular inflammation) characterized by the deposition of immune complexes consisting of IgA in kidney skin.
Lucia Pudyastuti Retnaningtyas
doaj +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
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
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

