Results 11 to 20 of about 9,015 (118)
Successful Treatment of Severe Purpura Fulminans With Anakinra
Pediatric Dermatology, EarlyView.ABSTRACT Purpura fulminans (PF) is a rare, often fatal pediatric condition characterized by intravascular thrombosis and hemorrhagic infarction of the skin. A timely diagnosis and treatment are paramount to prevent the involvement of internal organs, causing disseminated intravascular coagulation and gangrene of the extremities.
Francesco Zulian +4 more
wiley +1 more source
Impact of graft loss among kidney diseases with a high risk of post-transplant recurrence in the paediatric population [PDF]
, 2017 Background Some kidney diseases tend to recur in the renal allograft after transplantation. We studied the risk of graft loss among primary renal diseases known for their high risk of recurrence and compared it with that of patients with hypoplasia and ...
Belingheri, Mirco +13 more
core +1 more source
Journal of Internal Medicine, Volume 299, Issue 2, Page 271-282, February 2026.Abstract Background Studies suggest an increase in autoimmune diseases following SARS‐CoV‐2 infection and/or COVID‐19‐vaccination. We aimed to describe possible associations in Norway. Methods We used information from the emergency preparedness register for COVID‐19, BeredtC19, for all residents aged 18–64 (N = 3,450,080).
Håkon Bøås +4 more
wiley +1 more source
Protein-losing enteropathy associated with Henoch-Schönlein purpura [PDF]
, 2010 The gastrointestinal manifestations of Henoch-Schönlein purpura include abdominal pain, gastrointestinal bleeding, intussusception, and perforation. Protein-losing enteropathy is rarely associated with Henoch-Schönlein purpura.
Fuchigami, Tatsuo +2 more
core +3 more sources
Interdisciplinary Medicine, Volume 4, Issue 1, January 2026.This review systematically summarizes recent advances in aggregation‐induced emission (AIE) materials for in vitro diagnostics (IVD). It highlights probe design strategies—categorizing them into direct‐responsive, indirect‐responsive, and nano‐immunoprobes—and their applications in detecting a wide range of biomarkers across diverse body fluids ...
Qi Liu +5 more
wiley +1 more source
Púrpura de henoch-schonlein: revisão bibliográfica e relato de um caso. [PDF]
, 1998 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Minatto, André Caporal
core
Therapeutic advances in the treatment of vasculitis [PDF]
, 2016 Considerable therapeutic advances for the treatment of vasculitis of the young have been made in the past 10 years, including the development of outcome measures that facilitate clinical trial design.
Brogan, PA, Eleftheriou, D
core +2 more sources
Comprehensive multi‐omics mapping of immune perturbations in autism spectrum disorder
Clinical and Translational Medicine, Volume 15, Issue 12, December 2025.• Integrated multi‐omics profiling reveals systemic immune dysregulation in ASD, marked by an expansion of atypical immune cell subsets and activation of immune‐related pathways. • Significant alterations in peripheral immune cell populations are observed, including dysregulated NK cells, expanded CD56+ monocytes, and elevated MDSCs, and these changes ...
Chun Yan +12 more
wiley +1 more source
Vancomycin-induced Henoch-Schönlein purpura: a case report [PDF]
, 2012 Introduction Henoch-Schönlein purpura is a small-vessel systemic vasculitis. Although its exact pathophysiology remains unknown, Henoch-Schönlein purpura has been reported in association with various medical conditions including hypersensitivity.
Anne-Marie Tasei +18 more
core +3 more sources
Familial Mediterranean Fever Present with Gastrointestinal Manifestations of Henoch Schonlein Purpura [PDF]
, 2021 Henoch Schönlein Purpura is the most common small vessel vasculitis in childhood which is characterized with non-thrombocytopenic purpuric skin rash, arthritis, abdominal pain and renal disease.
Güzel, Yusuf +4 more
core +1 more source