Results 61 to 70 of about 2,477 (110)

The association of Behçet's syndrome with HLA-B51 as understood in 2021. [PDF]

Curr Opin Rheumatol, 2022
Takeno M.
europepmc   +1 more source

Behçet's Disease: A Rare Cause of Epididymo‐Orchitis

Trends in Urology &Men's Health, Volume 16, Issue 6, December 2025.
Ali S. Jawad
wiley   +1 more source

Ailesel sarkoidoz

Genel Tıp Dergisi, 2013
Sarkoidoz, nedeni tam olarak bilinmeyen ancak etiyolojisinde genetik, enfeksiyöz ajanlar, mesleksel maruziyet ve çevresel faktörlerin rol oynadığı multisistemik granülomatöz bir hastalıktır. Sarkoidozda ailesel yatkınlık bilinmekle beraber kalıtım şekli
Kürşat Uzun, Ayşe Uyanmış, Mustafa Dinç, Nadir Koçak, Mustafa Göktepe, Durdu Mehmet Yavşan   +5 more
doaj  

Behçet's disease risk-variant HLA-B51/ERAP1-Hap10 alters human CD8 T cell immunity. [PDF]

Ann Rheum Dis, 2022
Cavers A, Kugler MC, Ozguler Y, Al-Obeidi AF, Hatemi G, Ueberheide BM, Ucar D, Manches O, Nowatzky J.   +8 more
europepmc   +1 more source

ERAP1 Controls the Interaction of the Inhibitory Receptor KIR3DL1 With HLA-B51:01 by Affecting Natural Killer Cell Function. [PDF]

Front Immunol, 2021
D'Amico S, D'Alicandro V, Compagnone M, Tempora P, Guida G, Romania P, Lucarini V, Melaiu O, Falco M, Algeri M, Pende D, Cifaldi L, Fruci D.   +12 more
europepmc   +1 more source

Behcet's disease: demographic and genetic aspects (a literature review)

Современная ревматология, 2014
A review of literature focused on Behcet's disease (BD) is presented. BD is systemic vasculitis of unknown etiology affecting multiple organs. BD is endemic in the countries along the Eastern Mediterranean coast and the areas of Central and East Asia. We
Fatima Ismailovna Izmailova, Z S Alekberova   +1 more
doaj   +1 more source

From blindness to light: A clinical conundrum - central retinal vein occlusion as an initial manifestation of inflammatory bowel disease [PDF]

Romanian Medical Journal
This case report emphasizes central retinal vein occlusion (CRVO) as the primary cause of blindness, typically linked to impaired retinal venous drainage from critical vein obstruction.
Nithesh Babu Ramesh, Fathima S. Nilofar, Gnanadeepan Thirugnanam, Mahendra Kumar Kalappan, Venkateswaran A.R.   +4 more
doaj   +1 more source

Cerebral Aneurysms: A Rare Feature of Behçet's Disease—A Case Report and Review of the Literature

Case Reports in Neurological Medicine, 2013
Behçet's disease (BD) is a multisystem vascular inflammatory disease with several clinical manifestations. Intracranial aneurysms are an extremely rare but nevertheless severe complication of BD. We report a case of a 44-year-old man. The diagnosis of BD
Samia Younes, Yosra Cherif, Narjes Mokni, Olfa Berriche, Baha Zantour, Amel Boughammoura, Mahbouba Frih-Ayed, Saida Jerbi, Mohamed Habib Sfar   +8 more
doaj   +1 more source

Clinical Manifestations and Diagnosis of Behçet’s Syndrome

European Medical Journal Rheumatology, 2021
Behçet’s syndrome (BS) is a systemic vasculitis with a wide range of clinical presentations and disease courses. It may involve the mucosa, skin, joints, vessels, eyes, and nervous and gastrointestinal systems.
Sara Beça, Gerard Espinosa
doaj  

Coexistence of ankylosing spondylitis and Behçet's disease: Successful treatment with upadacitinib

Immunity, Inflammation and Disease
Background Ankylosing spondylitis (AS) and Behçet's disease (BD) are distinct inflammatory disorders, but their coexistence is a rare clinical entity. This case sheds light on managing this complex scenario with Janus kinase (JAK) inhibitors.
Krasimir Kraev, Petar Uchikov, Bozhidar Hristov, Maria Kraeva, Yordanka Basheva‐Kraeva, Stanislava Popova‐Belova, Milena Sandeva, Dzhevdet Chakarov, Snezhanka Dragusheva, Mariela Geneva‐Popova   +9 more
doaj   +1 more source