Results 61 to 70 of about 220,566 (226)

Higher Complement C4 Gene Copy Number Constitutes a Shared Genetic Risk Factor for Giant Cell Arteritis and IgA Vasculitis

open access: yesArthritis &Rheumatology, EarlyView.
Objective Low copy number (CN) of complement C4 isoforms and high CN of retroviral HERV‐K elements are known risk factors for many immune‐mediated inflammatory diseases (IMIDs), often showing sex‐biased effects. Here, we assessed whether CN variation within the C4 gene contributes to giant cell arteritis (GCA) and IgA vasculitis (IgAV), two complex ...
Laura Martínez‐Gutiérrez   +295 more
wiley   +1 more source

Characteristics of scrotal involvement in IgA vasculitis: Relationship with disease activity and inflammatory markers

open access: yesEuropean Journal of Pediatrics
Immunoglobulin A (IgA) vasculitis is a common systemic vasculitis in children, involving the skin, joint, gastrointestinal tract and kidneys. Scrotal involvement is a less common manifestation in the course of IgA vasculitis, which alters disease ...
Ş. Ertem   +10 more
semanticscholar   +1 more source

Comparative study on clinicopathological features and prognosis of IgA vasculitis nephritis and IgA nephropathy in children

open access: yesBMC Pediatrics, 2023
Background IgA vasculitis nephritis (IgAVN) and IgA nephropathy (IgAN) share several clinical and pathological characteristics, though distinctions also exist. Their interrelation, however, remains undefined.
Yan-li Lv   +5 more
semanticscholar   +1 more source

IgA vasculitis in children [PDF]

open access: yesBrazilian Journal of Nephrology, 2022
Maria Goretti Moreira Guimarães Penido   +1 more
openaire   +5 more sources

Differences in SARS‐CoV‐2 Antigen Persistence in Individuals With Systemic Autoimmune Rheumatic Diseases Compared to the General Population: A RECOVER‐Adult Cohort Study

open access: yesArthritis &Rheumatology, EarlyView.
Objective Individuals with systemic autoimmune rheumatic diseases (SARDs) are at risk for worse acute and post–acute COVID‐19 outcomes, though whether individuals with SARDs have longer persistence of viral antigens after COVID‐19 has not been studied.
Naomi J. Patel   +18 more
wiley   +1 more source

Intermittent abdominal pain in IgA vasculitis

open access: yesRevista Paulista de Pediatria, 2021
Objective: To assess intermittent abdominal pain in IgA vasculitis patients and its relation to demographic data, clinical manifestations and treatments.
Izabel Mantovani Buscatti   +9 more
doaj   +2 more sources

Short-term outcome of patients with adult IgA vasculitis: a single-center experience

open access: yesFrontiers in Medicine, 2023
Background Follow-up data on IgA vasculitis (IgAV) in adults are scarce. We aimed to investigate the outcome of adult IgAV in a well-defined cohort. Methods Data from histologically proven patients diagnosed between January 2010 and July 2022 with at ...
A. Hočevar   +4 more
semanticscholar   +1 more source

Rare vasculitis types and obstetric and neonatal outcomes – A population‐based study

open access: yesInternational Journal of Gynecology &Obstetrics, EarlyView.
Abstract Objective Vasculitis is an infrequent pathology among reproductive‐aged women. While data exists regarding pregnancy outcomes in the more common vasculitis subtypes, data is limited regarding these outcomes in rare vasculitis subtypes. We aimed to compare pregnancy and perinatal outcomes between women who suffered from rare types of vasculitis
Uri Amikam   +4 more
wiley   +1 more source

Henoch–Schönlein Purpura (IgA Vasculitis) in Association with Thyrotoxicosis

open access: yesCase Reports in Endocrinology, 2021
Graves’ disease is the most common cause of hyperthyroidism, which is characterized by thyroid antibodies and the following clinical manifestations: goiter, ophthalmopathy, and pretibial myxedema.
Mojgan Sanjari   +2 more
doaj   +1 more source

IgA vasculitis with nephritis: update of pathogenesis with clinical implications

open access: yesPediatric nephrology (Berlin, West), 2021
IgA vasculitis with nephritis (IgAVN) shares many pathogenetic features with IgA nephropathy (IgAN). The purpose of this review is to describe our current understanding of the pathogenesis of pediatric IgAVN, particularly as it relates to the four-hit ...
M. C. Hastings   +6 more
semanticscholar   +1 more source

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