Results 101 to 110 of about 4,852,263 (194)
When to consider an inborn error of immunity: clues for physicians
Abstract The term inborn errors of immunity (IEIs) refers to the rapidly expanding group of genetic disorders causing dysregulation of the immune system. With improved genetic testing in recent years, the number of defined IEIs and their range of phenotypic presentations has grown vastly, with more than 550 IEIs now described.
Meera Thangarajah, Lucinda J. Berglund
wiley +1 more source
Colon Perforation And Budd-Chiari Syndrome In Behçet’S Disease
Patient: Female, 38 , Final Diagnosis: Behçet’s disease , Symptoms: Severe abdominal pain • fever , Medication: — , Clinical Procedure: Parsiyel colectomy ...
Güney, Güven +9 more
core +1 more source
The Spectrum of Clinical Symptomatology in Patients with Neuro-Behcet’s Disease
Objective: To understand the pattern of neurological symptoms in patients diagnosed with Neuro-Behcet's disease. Study Design: Cross-sectional study. Duration and Place of Study: Pak Emirates Military Hospital Rawalpindi, from Jun 2013 to Jun 2018.
Jahanzeb Liaqat +4 more
doaj
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
Bimekizumab 2‐year efficacy by hidradenitis suppurativa duration: BE HEARD EXT results
Journal of the European Academy of Dermatology and Venereology, EarlyView.
Raj Chovatiya +9 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
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 syndrome is a systemic inflammatory panvasculitis (affecting all sizes of vessels) of unknown aetiology. It is in vogue to include it among the systemic autoinflammatory conditions.
Hasan Yazici +2 more
core +1 more source
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
Demographic features and clinical aspects of Behçet’s disease in Omani patients
Objectives: Behçet’s disease is a chronic, relapsing, multisystem vasculitis of unknown etiology. Few reports support the hypothesis that Behçet’s disease has a primarily hereditary basis.
Humaid Al Wahshi, Aadil Al Ghafri
core +1 more source

