Results 61 to 70 of about 101,671 (163)

Bilateral Retrobulbar Optic Neuritis as the First Manifestation of Neuro-Behçet Disease

Case Reports in Rheumatology, 2020
Background. Behçet disease (BD) is a polygenic and chronic autoinflammatory multisystem vasculitis. Acute optic neuritis has been rarely reported in patients with BD, especially in children. Case Presentation. We reported an 8-year-old girl with a sudden
Mohsen Jari, Taiiebeh Mohammadi, Ensiyeh Taheri   +2 more
doaj   +1 more source

Nomenclature for Factors of the HLA System, 2026

HLA, Volume 107, Issue 3, March 2026.
Steven G. E. Marsh, Kazutoyo Osoegawa, Walter F. Bodmer, Ronald E. Bontrop, Mary N. Carrington, Henry A. Erlich, Sebastiaan Heidt, Rhonda Holdsworth, Wolfgang R. Mayr, Martin Maiers, Peter Parham, Effie W. Petersdorf, James Robinson, John Trowsdale, Marcelo Fernández‐Viña   +14 more
wiley   +1 more source

Atypical Pediatric‐Onset Behçet's Disease Presenting With Superior Vena Cava Thrombosis in an Adolescent Male: A Case Report

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Behçet's disease is a chronic, relapsing multisystem vasculitis known for its highly variable clinical spectrum. We report the case of an 18‐year‐old male who presented with progressive headache and facial swelling. Imaging revealed extensive thrombosis involving the dural venous sinuses, superior vena cava, and left brachiocephalic vein ...
Ubaid Ullah, Tahreem Mari, Ubaid Ullah Mian, Aizaz Ali, Samra Aleem, Tarmim Lal, Abdul Moeez, Tanzeela Begum, Jibran Ikram   +8 more
wiley   +1 more source

Long-Term Outcomes of Behçet’s Syndrome-Related Uveitis: A Monocentric Italian Experience

Mediators of Inflammation, 2020
Objectives. To examine demographic and clinical characteristics and long-term visual outcome in a cohort of Italian patients affected by Behçet’s uveitis (BU). Materials and Methods.
Jurgen Sota, Luca Cantarini, Antonio Vitale, Arianna Sgheri, Stefano Gentileschi, Valeria Caggiano, Viviana Gelardi, Bruno Frediani, Gian Marco Tosi, Claudia Fabiani   +9 more
doaj   +1 more source

HLA types in Turkish children with celiac disease

The Turkish Journal of Pediatrics, 2008
The aim of this study was to assess the distribution of human leukocyte antigen (HLA) groups in Turkish children with celiac disease (CD) and to investigate the association of HLA types and clinical manifestations of CD. Seventy-five children with
Zarife Kuloğlu, Tümay Doğanci, Aydan Kansu, Fulya Demirçeken, Murat Duman, Hüseyin Tutkak, Arzu Ensari, Nurten Girgin   +7 more
doaj  

Descubriendo el Síndrome de Behçet. Reporte de caso de una enfermedad rara en Colombia

Biociencias
Introducción: El síndrome de Behçet es un trastorno multisistémico de etiología desconocida clasificado como vasculitis de vaso variable, que se caracteriza por úlceras orales y genitales, lesiones cutáneas y manifestaciones oftalmológicas ...
Luisa Fernanda Jiménez Arcia, Estiven de Jesús Crespo Vizcaíno, Carlos José Brito Jácome, Evis Adriana Castellón de la Rosa   +3 more
doaj   +1 more source

Epistatic interaction of ERAP1 and HLA-B in Behçet disease: a replication study in the Spanish population.

PLoS ONE, 2014
Behçet's disease (BD) is a multifactorial disorder associated with the HLA region. Recently, the ERAP1 gene has been proposed as a susceptibility locus with a recessive model and with epistatic interaction with HLA-B51.
Marta Conde-Jaldón, Marco Antonio Montes-Cano, José Raul García-Lozano, Lourdes Ortiz-Fernández, Norberto Ortego-Centeno, Rocío González-León, Gerard Espinosa, Genaro Graña-Gil, Juan Sánchez-Bursón, Miguel Angel González-Gay, Ana Celia Barnosi-Marín, Roser Solans, Patricia Fanlo, Mónica Rodríguez Carballeira, Teresa Camps, Santos Castañeda, Javier Martín, María Francisca González-Escribano   +17 more
doaj   +1 more source

Delayed Massive Haemoptysis Following EBUS‐TBNA Revealing a Pseudoaneurysm of an Ectopic Bronchial Artery: A Rare Complication at the Crossroads of Interventional Pulmonology and Radiology

Respirology Case Reports, Volume 13, Issue 12, December 2025.
A 31‐year‐old woman with Budd–Chiari syndrome developed delayed massive haemoptysis 1 week after EBUS‐TBNA due to pseudoaneurysms arising from 4R lymph nodes. Diagnosis was confirmed by CT angiography and bronchoscopy, and successful microcoil embolisation achieved complete resolution.
Julien G. Cohen, Matthieu Papillard, Romain Messe   +2 more
wiley   +1 more source

The evaluation of HLA class I association with allergic Asthma

مجله دانشگاه علوم پزشکی گرگان, 2002
Major histocompatibility complex (MHC), which plays a major biological function in immune response, is generally associated with so many human disease. During recent years a new clinical relevance of MHC disease.
E.Alijani (M.Sc), M.Shekarabi (Ph.D), M.Kamgooyan (M.Sc), S.Arshi (M.D), M.Jafari-Modrek (M.Sc)   +4 more
doaj  

Rare Wound: Extensive Skin Lesions and Poor Wound Healing of the Calf in a Patient With Behçet's Disease

International Wound Journal, Volume 23, Issue 2, February 2026.
Xian Sun, Yang Xia, Jia‐Jun Wu, Ke‐Jia Li   +3 more
wiley   +1 more source