Results 31 to 40 of about 1,239,123 (172)

Behçet’s Disease-related Budd–Chiari Syndrome Successfully Managed with anti-TNF Antibody: A Case Report and Review of the Literature

, 2022
Behçet’s disease (BD) is multisystemic vasculitis with heterogeneous clinical manifestations. We describe the case of a 26-year-old man who presented with Budd–Chiari syndrome (BCS) related to BD. The patient received infliximab (IFX) due to the severity
Uzun, Gullu Sandal, Keskin, Onur, Koksal, Deniz, Erul, Enes, Kalyoncu, Umut, Inkaya, Ahmet Cagkan, Uysal, Serkan   +6 more
core   +1 more source

Syndrome In Question [PDF]

Anais Brasileiros de Dermatologia, 2014
The authors present a male 40-year-old patient with established diagnosis of Behçet's disease which had evolved to recurrent bilateral auricular polychondritis crises.
Ana Claudia Mendes do Nascimento, Daniela Barros Cortez Gaspardo, Tatiana Mimura Cortez, Helio Amante Miot   +3 more
doaj   +1 more source

Budd-Chiari syndrome in association with Behçet's disease: review of the literature

São Paulo Medical Journal
The risk that patients with Behçet's disease may develop various thrombotic complications has been previously described. Although vascular complications from Budd-Chiari syndrome associated with Behçet's disease have been described, the pathogenic ...
Daniela Carvalho, Fernando Oikawa, Nilce Mitiko Matsuda, Alice Tatsuko Yamada   +3 more
doaj   +1 more source

Behçet’s syndrome

, 2010
Behçet’s syndrome is an inflammatory disorder of unknown aetiology that involves arteries and veins of all sizes. Most cases are from the countries around the Mediterranean basin, the Middle East and east Asia, with the highest prevalence in Turkey.
Hasan Yazici, Sebahattin Yurdakul, Izzet Fresko   +2 more
core   +1 more source

Evaluation of the Thyroid Gland in Patients with Behcet’s Syndrome

Endocrinology Research and Practice, 2005
Behcet’s Syndrome is a chronic, progressive, recurrent syndrome that can affect all organs and that histopathologically proceeds with vasculitis. Its etiology and pathogenesis is still unknown.
Yusuf Özkan, Ramis Çolak, Yunus Saral, Başak Kandi Coşkun, Orhan Kürşad Poyrazoğlu   +4 more
doaj   +2 more sources

Discordance Between Patient and Physician Global Assessments in Early Systemic Sclerosis

Arthritis Care &Research, EarlyView.
Objective This study aims to identify factors associated with patient global assessment (PtGA) and physician global assessment (PhGA) and discordance between them in systemic sclerosis (SSc). Methods Data from adults with early SSc (<5 years) from the Collaborative National Quality and Efficacy Registry were included.
Ellen Romich, Alexis Ogdie, Alisa Stephens Shields, Peter A. Merkel, Shervin Assassi, Elana J. Bernstein, Andreea Bujor, Flavia V. Castelino, Lorinda Chung, Luke B. Evnin, Tracy M. Frech, Jessica K. Gordon, Melissa Griffith, Faye N. Hant, Monica L. Harding, Laura K. Hummers, Dinesh Khanna, Kimberly S. Lakin, Dorota J. Lebiedz‐Odrobina, Yiming Luo, Ashima Makol, Maureen D. Mayes, Zsuzsanna H. McMahan, Jerry Molitor, Duncan F. Moore, Julie Paik, Carrie Richardson, Brian Skaug, Ami A. Shah, Ankoor Shah, Virginia Steen, John M. VanBuren, Elizabeth R. Volkmann, Carleigh Zahn, Nora Sandorfi, for the CONQUER Investigators   +35 more
wiley   +1 more source

MSJ786058_supplementary_table_1 – Supplemental material for Primary optic neuropathy in Behçet’s syndrome

, 2018
Supplemental material, MSJ786058_supplementary_table_1 for Primary optic neuropathy in Behçet’s syndrome by Qinglin Yang, Lin Sun, Qian Wang, Jiawei Wang, Chao Meng, Qinglin Chang, Xuehui Shi, Shilei Cui, Lei Liu and Chuntao Lai in Multiple Sclerosis ...
Chao Meng (467013), Lei Liu (4213336), Qian Wang (32718), Qinglin Chang (815818), Chuntao Lai (815817), Xuehui Shi (5500157), Shilei Cui (846480), Jiawei Wang (158148), Lin Sun (105539), Qinglin Yang (811623)   +9 more
core   +1 more source

Early versus late initiation of infliximab for refractory uveitis in a cohort of Egyptian BD patients

Journal of the Egyptian Ophthalmological Society
Introduction Behçet’s syndrome is a multisystem inflammatory disease characterized by recurrent oral aphthous ulcers, genital ulcers, skin lesions, and uveitis.
Mariam R Fadel, Shereen H AboulNaga, Nehal ElGhobashy, Sally S. Mohamed   +3 more
doaj   +1 more source

Distribution of Behçet's Syndrome in the World and in Iran: A Systematic Review and Meta Analysis [PDF]

Taṣvīr-i salāmat, 2016
​Background and objectives : Behçet's syndrome is an inflammatory disorder of unknown etiology that has a unique worldwide prevalence and distribution.
Dorna Ghafari, Behrooz Sari Sarraf, Zhila Khamnian, Roya Dolatkhah, Parastoo Moradi, Soraya Hadi, Saeid Dastgiri   +6 more
doaj  

MSJ786058_supplementary_figures – Supplemental material for Primary optic neuropathy in Behçet’s syndrome

, 2018
Supplemental material, MSJ786058_supplementary_figures for Primary optic neuropathy in Behçet’s syndrome by Qinglin Yang, Lin Sun, Qian Wang, Jiawei Wang, Chao Meng, Qinglin Chang, Xuehui Shi, Shilei Cui, Lei Liu and Chuntao Lai in Multiple Sclerosis ...
Chao Meng (467013), Lei Liu (4213336), Qian Wang (32718), Qinglin Chang (815818), Chuntao Lai (815817), Xuehui Shi (5500157), Shilei Cui (846480), Jiawei Wang (158148), Lin Sun (105539), Qinglin Yang (811623)   +9 more
core   +1 more source