Results 61 to 70 of about 1,239,123 (172)
Introduction: Behçet’s disease was initially described by Behçet as a triad of symptoms, including recurring oral ulcers, recurring genital ulcers, and ocular involvement.
Parichehr Ghalyani, Fatemeh Babadi
doaj
Delphi consensus: First‐line use of biologics and small molecules in hidradenitis suppurativa
This Delphi Consensus study identified upgrade criteria for the use of biologics and small molecules as first‐line therapy in hidradenitis suppurativa (HS). European HS experts evaluated 16 clinical scenarios, voting on eligibility for therapy escalation.
Georgios Nikolakis +54 more
wiley +1 more source
This study aims to describe musculoskeletal manifestations (MSM) in children with Behçet’s syndrome (BS), their association with other disease manifestations, response to therapy, and long-term prognosis.
Karadeniz, H. +56 more
core
BEHÇET’S SYNDROME AND THROMBOSIS
<h2 style="line-height: 200%; margin: 10pt 0cm 0pt;"><span style="line-height: 200%; font-family: " lang="EN-US">Behçet syndrome (BS) is a multisystem vasculitis with unknown etiology and a unique geographic distribution.
Emire Seyahi, Sebahattin Yurdakul
doaj +3 more sources
Measuring success in HS treatment from the physician's and the patient's perspective
Integrated clinician (HiSCR, IHS4, IHS4‐55, HS‐IGA) and patient (HiSQOL, DLQI) scores, combined with imaging‐based fibrosis and inflammation assessment, redefine treatment success in hidradenitis suppurativa by aligning treat‐to‐target strategies with both inflammatory control and irreversible structural damage.
Georgios Nikolakis +4 more
wiley +1 more source
Behcet’s Syndrome resembling complex perianal Crohn’s Disease
Behcet’s syndrome is a systemic inflammatory disorder that involves several organ systems and is exceptionally rare in the Western world. The diagnosis is frequently difficult as it resembles several other disease processes.
Ali P Mourad +2 more
doaj +1 more source
Treatment strategies for interstitial granulomatous dermatitis: Systematic review and expert opinion
Systematic review of 108 studies with a total of 182 patients with interstitial granulomatous dermatitis (IGD). IGD was frequently associated with systemic conditions or drug exposure. Management includes careful medication review and prompt withdrawal of potential triggers. Corticosteroids (systemic and topical) were commonly effective, while biologic
Francesco Bellinato +4 more
wiley +1 more source
Behçet’s syndrome: one year in review 2024
The aim of this review is to provide a critical summary of studies published during 2023 that contribute to our understanding of Behçet’s syndrome. An increase in the incidence of BS was reported in Northern Spain after 2014.
Talarico, R. +5 more
core +1 more source
Modulation of sebocyte function in acne: A pathway‐inclusive review
Acne is multifactorial, with the sebocyte acting as a central immunometabolic hub linking lipogenic, inflammatory, hormonal and barrier pathways. Mapping established and investigational therapies onto this sebocyte‐centred model offers a mechanism‐based framework that complements existing treatment paradigms and may guide more targeted, antibiotic ...
Christos C. Zouboulis +3 more
wiley +1 more source
AI‐assisted reading with the open‐source SEE‐AI model improves lesion detection sensitivity and reduces reading time in small‐bowel capsule endoscopy. In a multicenter retrospective study of 249 cases, SEE‐AI provides visual cues that support physicians during interpretation while preserving physician‐led final decisions.
Satoshi Miyazono +19 more
wiley +1 more source

