Results 81 to 90 of about 9,673 (180)
Case for diagnosis Caso para diagnóstico
Anais Brasileiros de Dermatologia, 2012 Henoch-Schönlein Purpura (HSP) is the most common vasculitis in children. In the absence of significant renal disease it has an excellent prognosis. In the case described, HSP initially presented together with orchitis. This infrequent event required the
Gustavo Januário, Felicidade Santiago
doaj +1 more source
ClinicsOBJECTIVES: Henoch-Schönlein purpura nephritis and immunoglobulin A nephropathy are two diseases with similar clinical presentations but very different prognoses.
Zhao Shuiai +4 more
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مجله دانشکده پزشکی اصفهان, 2018 Background: Henoch-Schonlein purpura (HSP) is a common childhood systemic vasculitis with clinical characteristics of cutaneous palpable purpura, arthralgia/arthritis, abdominal pain, and renal involvement.
Tooba Momen, Mohsen Jari, Hasan Nasimi
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Noninvasive Urinary Monitoring of Progression in IgA Nephropathy. [PDF]
, 2019 Standard methods for detecting and monitoring of IgA nephropathy (IgAN) have conventionally required kidney biopsies or suffer from poor sensitivity and specificity.
Fervenza, Fernando C +4 more
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Urticarial Systemic Allergic Dermatitis Following Mitomycin C Instillation
Contact Dermatitis, Volume 93, Issue 5, Page 433-435, November 2025.
Dani Heuts +4 more
wiley +1 more source
Haemorrhagic Bullous Lesion in Henoch-Schonlein Purpura
Berkala Ilmu Kesehatan Kulit dan Kelamin (Periodical of Dermatology and Venerology), 2016 Background: Henoch-Schonlein purpura (HSP) is a vasculitis of the small vessels and the most common type of vasculitis in children. Vesicles and haemorrhagic bullae were thought to be rare in HSP and maybe difficult to diagnose.
Renata Prameswari +2 more
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The association of complement with common connective tissue diseases - a review [PDF]
, 2008 Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/OpenA strong association has been found between complement and common connective tissue diseases, such as systemic lupus erythema and Henoch Schoenlein Purpura ...
Guðmundur Jóhann Arason
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The Turkish Journal of Pediatrics, 2010 We aimed to analyze the Toll-like receptor (TLR)2 and TLR4 expressions, which are known to be involved in the recognition of pathogens by the innate immune system, in patients with Henoch-Schönlein purpura.
Hande Canpinar +4 more
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Streptococcus pyogenes as the aetiological agent of Henoch–Schönlein purpura
Pediatria i Medycyna Rodzinna, 2017 Henoch–Schönlein purpura is a systemic disease mainly affecting school age children. It is characterised by leukocytoclastic small-vessel vasculitis with the deposition of IgA-containing immune complexes in cutaneous, gastrointestinal, articular and ...
Aleksandra Kundera +4 more
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Characteristics of articular syndrome in systemic vasculitis [PDF]
, 2017 The purpose of the study – investigation the separate joint lesion in systemic vasculitis, their X-ray sonographic characteristics, the correlation of the articular syndrome severity with extra-articular manifestations of the diseases, as well as ...
Gashynova, K. +4 more
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