Results 111 to 120 of about 220,566 (226)

Deregulation in adult IgA vasculitis skin as the basis for the discovery of novel serum biomarkers

Arthritis Research & Therapy
Introduction Immunoglobulin A vasculitis (IgAV) in adults has a variable disease course, with patients often developing gastrointestinal and renal involvement and thus contributing to higher mortality.
M. Bajželj, M. Hladnik, R. Blagus, V. Jurčič, Ana Markež, T. D. Toluay, S. Sodin‐Šemrl, A. Hočevar, K. Lakota   +8 more
semanticscholar   +1 more source

Palbociclib-induced IgA vasculitis

Dermatology Online Journal, 2022
Patel, Payal M, Kelm, Ryan C, Amber, Kyle T   +2 more
openaire   +4 more sources

Correlation between antiphospholipid antibodies and renal involvement in children with Henoch-Schönlein purpura: A cross-sectional study [PDF]

Caspian Journal of Internal Medicine
Background: Renal involvement is the most damaging long-term complication of Immunoglobulin-A (IgA) vasculitis. In the lack of a definite predictive biomarker for renal involvement, antiphospholipid antibodies (aPL) have been proposed in recent years ...
Mehrnoush Hassas Yeganeh, Reza Sinaei, Aye Yaraghi, Khosro Rahmani, Vadood Javadi Parvaneh, Reza Shiari, Hamid Hosseinzadeh   +6 more
doaj  

Insight into the Interplay of Gd-IgA1, HMGB1, RAGE and PCDH1 in IgA Vasculitis (IgAV)

International Journal of Molecular Sciences
The pathogenesis of IgAV, the most common systemic vasculitis in childhood, appears to be complex and requires further elucidation. We aimed to investigate the potential role of galactose-deficient immunoglobulin A1 (Gd-IgA1), high-mobility group box 1 ...
M. Held, A. Kozmar, M. Šestan, D. Turudić, N. Kifer, S. Srsen, A. Gagro, M. Frković, M. Jelušić   +8 more
semanticscholar   +1 more source

Vasculitis por IgA con compromiso gastrointestinal en un adolescente: Reporte de un caso y revisión de la literatura

Revista Reumatología al Día
La vasculitis por IgA es la vasculitis sistémica más frecuente en la edad pediátrica y adolescencia, caracterizada por depósito de inmunocomplejos de IgA en vasos de pequeño calibre.
Kerly Janina Cruz Mayor, José Franco Litardo   +1 more
doaj   +1 more source

Annular and Purpuric Plaques with Systemic Symptoms: A Unique Presentation of Immunoglobulin A Vasculitis

Journal of Dermatology and Dermatologic Surgery
A male in his 20s presented to the hospital with a rash, abdominal pain, blood in the stool, and fatigue. The rash, originally diagnosed as urticarial vasculitis, developed 4 months prior and had been treated with several courses of low-dose steroids ...
Rachel V. Goff, Eliana F. Zamora, Cindy Owen   +2 more
doaj   +1 more source

Glucocorticoids in IgA vasculitis

Acta Medica
IgA vasculitis (IgAV) is an immune complex vasculitis affecting small vessels characterized by IgA1 immune deposits. IgA vasculitis typically resolves spontaneously in most cases, especially in pediatric cases but may have more severe outcomes in adults and the optimal treatment for IgAV remains controversial.
openaire   +1 more source

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Ultraviolet Purpura in IgA Vasculitis [PDF]

Mayo Clinic Proceedings, 2018
Daisuke, Tsukui, Hajime, Kono
openaire   +2 more sources