Results 61 to 70 of about 15,099 (182)
Exploring the Shared Genetic Basis of Age at Menopause and Osteoarthritis
ACR Open Rheumatology, Volume 8, Issue 7, July 2026.Objective The relationship between age at menopause and osteoarthritis (OA) remains unclear. Methods The genetic commonalities between age at menopause and OA were investigated using data from publicly accessible genome‐wide association studies. A variety of methods were employed in this exploration, such as linkage disequilibrium score regression ...
Bingru Luo +3 more
wiley +1 more source
Scurvy masquerading as IgA vasculitis
Pediatric RheumatologyAbstract Background Vitamin C deficiency, or scurvy, is rare but poses risks for children with poor diets, limited resources, or malabsorption issues. It may also be common in children with restrictive or selective dietary habits in children with global developmental delay, autism spectrum disorder, and physical ...
Hanna L. Kassa +10 more
openaire +3 more sources
A Painful Purpuric Rash in a Febrile Smoker
JEADV Clinical Practice, EarlyView.
Eugerta Dilka +3 more
wiley +1 more source
A Review and Future Perspective on Renal Outcome Definitions in Lupus Nephritis
ACR Open Rheumatology, Volume 8, Issue 7, July 2026.Lupus nephritis (LN) remains a leading cause of morbidity and mortality in systemic lupus erythematosus, yet the lack of standardized definitions for renal outcomes hinders effective diagnosis, prognosis, treatment personalization, comparisons across trials, and interpretable trial endpoints.
Ioannis Parodis +4 more
wiley +1 more source
Arthritis &Rheumatology, Volume 78, Issue 7, Page 1393-1402, July 2026.Sjögren disease (SjD) is a common systemic autoimmune disorder characterized by inflammation of the exocrine glands, resulting in dryness. Patients frequently exhibit extraglandular manifestations affecting various organ systems. To date, there are no US Food and Drug Administration (FDA)‐approved disease‐modifying therapies for SjD. In this review, we
Rachael A. Gordon, Sara S. McCoy
wiley +1 more source
Exercise‐induced vasculitis with histological and genetic evidence of complement involvement
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Massimo Cugno +6 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT A 12‐year‐old boy presented with recurrent oral and scrotal ulcers, papulopustular lesions, arthralgia, and a positive pathergy test. Autoimmune tests were negative; ophthalmologic and gastrointestinal assessments were reassuring. Topical therapy and colchicine produced sustained improvement.
Fares Basel Abu Taha +8 more
wiley +1 more source
Fasciitis as a Complication of IgA Vasculitis
CureusImmunoglobulin A vasculitis (IgAV) is a systemic small-vessel vasculitis caused by the deposition of IgA-based immune complexes, with myalgia being a rare complication. This study reports a pediatric case of IgAV with fasciitis. A five-year-old boy with no previous medical history was admitted to the hospital with abdominal pain and repeated bilious ...
Nii, Kohichiroh +4 more
openaire +2 more sources
Suspected Alcohol-Induced Immunoglobulin A Vasculitis: A Case Series and Review of the Literature
Case Reports in DermatologyIntroduction: Immunoglobulin A (IgA) vasculitis is a small vessel leukocytoclastic vasculitis marked by IgA-dominant immune complex deposition, typically affecting the skin, joints, gastrointestinal tract, and kidneys.
Aidan Maxwell, Kent Axcell, Matthew Helm
doaj +1 more source
Advances in Rheumatology, 2019 Background The Henoch-Schönlein Purpura (HSP) orIgA vasculitis is the most common vasculitis of childhood and may occur with renal involvement, with hematuria and / or proteinuria, and may cause severe and non-reversible sequelae. Objectives To establish
Vânia Schinzel +6 more
doaj +1 more source