Results 111 to 120 of about 4,851,513 (185)
Pseudo-Kaposi's sarcoma in Behçet's disease
Thrombosis in BehÇet's disease (BD) is not uncommon and venous occlussions affecting the venae cavae and their tributaries may result in during the course of the disease.
Süleyman Özbek +3 more
core +1 more source
Mapping the Altered Landscape of TCR Repertoire in Autoimmune Diseases
ABSTRACT Autoimmune diseases arise from the breakdown of immune tolerance through complex interactions between genetic predisposition, environmental exposures, and adaptive immune responses. High‐throughput T‐cell receptor (TCR) repertoire sequencing has transformed our ability to characterize these responses, providing unprecedented insights into ...
Celine Albalaa +3 more
wiley +1 more source
Tubulointerstitial Nephritis With Uveitis (TINU) Syndrome: A Case Series and Review of Literature
ABSTRACT Tubulointerstitial nephritis with uveitis (TINU) syndrome is a rare disorder characterised by the simultaneous or sequential occurrence of acute tubulointerstitial nephritis and uveitis, in the absence of systemic disease. Its true prevalence is likely underestimated, as renal and ocular manifestations may not appear concurrently. We conducted
Weaam Ali +5 more
wiley +1 more source
Lymphocyte gamma-glutamyl transferase activity in Behçet's disease.
In this study the activity of a membrane-bound enzyme, gamma-glutamyl transferase GGT (gamma-glutamyl transpeptidase - GGTP), was investigated in the peripheral blood lymphocytes (PBL) from patients with Behçet's disease.
Karan A. +3 more
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ABSTRACT Background Complex regional pain syndrome type 1 (CRPS1) is a disabling pain syndrome whose treatment remains challenging. Mesotherapy is a therapeutic method involving the injection of low doses of active substances through the skin. No studies assessed mesotherapy in CRPS1 patients.
Philippe Lafuma +12 more
wiley +1 more source
Behçet’s disease, also known as the oral–ocular–genital syndrome, is a chronic systemic vasculitis characterized by recurrent oral and genital ulcers as well as ocular manifestations such as uveitis and conjunctivitis.
Dou Yuan
doaj +1 more source
We report an autopsy case of VEXAS syndrome presenting with aggressive clinical course. Pathologically, the disease manifested as systemic granulocytic vasculitis affecting both arteries and veins, characterized by the presence of histiocytoid myeloid cells associated with low‐risk MDS.
Kayo Ueda +5 more
wiley +1 more source
TWO CASES COMBINED WITH BEHCET’S DISEASE AND RHEUMATIC VALVULAR HEART DISEASE WERE DIAGNOSED
Recent studies have revealed that streptococci play an important role in the etiology of Behcet's disease. As it is known, rheumatic valvular heart disease results from carditis occuring after group A streptococcal infections.
Engin Bozkurt +2 more
doaj
ABSTRACT Objectives This study aimed to determine the effects of caregiver burden on the healthy lifestyle behaviours of people caring for patients with Alzheimer's disease. Methods The Caregiver Burden Inventory (CBI) and the Healthy Lifestyle Behaviour Scale‐II (HLBS‐II) were administered to caregivers of Alzheimer's disease patients who were ...
Büşra Neva Tekin +3 more
wiley +1 more source
New insights in the clinical understanding of Behçet's disease [PDF]
Behçet's disease is a chronic relapsing multisystemic inflammatory disorder characterized by four major symptoms (oral aphthous ulcers, genital ulcers, skin lesions, and ocular lesions) and occasionally by five minor symptoms (arthritis, gastrointestinal
방동식, 조성빈
core

