Results 51 to 60 of about 8,434 (216)

Oxford Classification of IgA Nephropathy Is Applicable to Predict Long-Term Outcomes of Henoch-Schönlein Purpura Nephritis

Iranian Journal of Allergy, Asthma and Immunology, 2014
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  

A POSSIBLE RELATIONSHIP BETWEEN SERUM HOMOCYSTEINE LEVEL AND IgA NEPHROPATHY IN CHILDREN

İstanbul Tıp Fakültesi Dergisi, 2021
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, Zeynep Nagehan Yürük Yıldırım, Alev Yılmaz, Asuman Gedikbaşı, Nurinisa Karagöz, Nurver Akıncı, Aysel Kıyak, Gül Özçelik, Mesude Yasemin Özlük, Işın Kılıçaslan, Ayşe Ayşim Özağarı, Bağdagül Yavaş Aksu, Sevinç Emre   +12 more
doaj   +1 more source

Bartonella seropositivity in children with Henoch-Schonlein purpura [PDF]

BMC Infectious Diseases, 2005
Abstract Background An association between Henoch-Schonlein purpura (HSP) and seropositivity for Bartonella henselae (BH) has been described. The objective of this study was to see if such an association exists in northern Alberta. Methods
McColl Dorothy, Prasad Errol, Spady Donald W, Robinson Joan L, Artsob Harvey   +4 more
openaire   +3 more sources

Does clinical exposure to different skin tones during training improve diagnostic ability?

Medical Education, Volume 60, Issue 4, Page 410-417, April 2026.
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, Anna Coulson, Bethan Trigg, Nariell Morrison, Adam Potts, Moira Pain, Olamide Oguntimehin, Eleanor J. Hothersall‐Davies, Richard Hankins, Celia A. Brown, Amir H. Sam   +10 more
wiley   +1 more source

Safety of Immune Checkpoint Inhibitors in Cancer Patients With Preexisting Autoimmune Vasculitis

ACR Open Rheumatology, Volume 8, Issue 3, March 2026.
Objective Immune checkpoint inhibitors (ICIs) are effective cancer therapies but often cause serious immune‐related adverse events (irAEs). Patients with preexisting autoimmune diseases, including vasculitis, are excluded from trials. We aimed to evaluate the frequency, severity, and outcomes of vasculitis flares and irAEs in this population.
Juan Sevillano, Noha Abdel‐Wahab, Yixuan Zhou, Juan I. Ruiz, Maria E. Suarez‐Almazor   +4 more
wiley   +1 more source

Henoch–Schonlein Purpura Leads to Functional Gastrointestinal Disorders

, 2010
Pain predominant functional gastrointestinal disorders such as irritable bowel syndrome may develop as sequelae to acute infectious gastroenteritis. Henoch-Schonlein purpura is a vaculitis that causes an inflammatory insult to the intestinal mucosa.
Saps, Miguel, Ashish Chogle, Miguel Saps, Chogle, Ashish, Gati Dhroove, Dhroove, Gati   +5 more
core   +1 more source

Fractional Microneedling Radiofrequency for Hidradenitis Suppurativa: A Real‐World Retrospective Study Demonstrating Clinical Efficacy and Safety Across Diverse Anatomical Sites

Journal of Cosmetic Dermatology, Volume 25, Issue 3, March 2026.
ABSTRACT Background Hidradenitis suppurativa (HS) remains a therapeutically challenging disease despite expanding research and evolving systemic treatments. Energy‐based modalities, such as fractional microneedling radiofrequency (FMR), are being increasingly explored as novel treatment options.
Ari Safir, Eyal Taleb, Daniella Berzin, Manny Arieli, Aspasia Liassidou, Waseem Shehadeh, Ariela Hafner, Ofir Artzi   +7 more
wiley   +1 more source

Successful Treatment of Severe Purpura Fulminans With Anakinra

Pediatric Dermatology, Volume 43, Issue 2, Page 421-424, March/April 2026.
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, Luca Spiezia, Antonio Amabile, Francesca Tirelli, Alessandra Meneghel   +4 more
wiley   +1 more source

Cerebral Vasculitis in Henoch-Schonlein Purpura: A Case Report

, 2017
Henoch-Schonlein purpura is a common form of systemic small vessel vasculitis in childhood. Although headache and behavioral changes have been described in a significant proportion of children with Henoch-Schonlein purpura, severe neurological ...
Akcaboy, Meltem and Fidan, Kibriya and Kandur, Yasar and Isiyel, Emel and Buyukkaragoz, Bahar and Ezgu, Sevcan Azime Bakkaloglu and Buyan, Necla and Hasanoglu, Enver and Soylemezoglu, Oguz
core   +1 more source

Recurrent adult onset Henoch-Schonlein Purpura: a case report [PDF]

, 2016
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, Gaskill, Neil, Mago, Cynthia   +2 more
core   +1 more source