Results 61 to 70 of about 1,144,913 (219)

Severe panuveitis in neuro-Behçet’s disease in Malaysia: a case series

International Medical Case Reports Journal, 2017
Khairuddin Othman,1 Ahmad Tajudin Liza-Sharmini,1 Mohtar Ibrahim,1 John Tharakan,2 Ryoji Yanai,3 Embong Zunaina1 1Department of Ophthalmology, 2Department of Neurosciences, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan ...
Othman K, Liza-Sharmini AT, Ibrahim M, Tharakan J, Yanai R, Zunaina E   +5 more
doaj  

Inflammation Unchecked: Concurrent Kawasaki Disease and Stevens‐Johnson Syndrome in an 18‐Month‐Old Child

Arthritis Care &Research, EarlyView.
Catherine Deffendall, Jodi Backalar, Elizabeth Acevedo Zapata, Adriana Della Porta, Lorin Bibb, Tyler Reese, Charlotte M. Brown   +6 more
wiley   +1 more source

Factors Associated With Bilateral Involvement in Non‐Infectious Labyrinthitis: A Case–Control Study

The Laryngoscope, EarlyView.
Non‐infectious labyrinthitis may progress from unilateral to bilateral inner‐ear involvement, resulting in greater functional impairment. In this retrospective case–control study of 50 patients, younger age, female sex, and the presence of systemic disease were associated with bilateral involvement. These exploratory findings may help identify patients
Douglas Henderson, Blanca Amador Borrero, Aurélien Cadix, Karine Champion, Damien Sene, Philippe Herman, Charlotte Hautefort, Alain Londero, Michael Eliezer, Cassandre Djian   +9 more
wiley   +1 more source

How to treat myelodysplastic syndrome with clinical features resembling Behcet syndrome: a case-based systematic review

, 2020
The association between myelodysplastic syndrome (MDS) and Behcet syndrome (BS) is recognized for over 25 years. High frequency of trisomy 8 and intestinal ulcers are striking features of this association.
HATEMİ, Gülen, ERZİN, Yusuf Ziya, ÇELİK, Aykut Ferhat, AR, Muhlis Cem, Yılmaz, Umut, Esatoglu, Sinem Nihal, BAVUNOĞLU, Işıl, Yıldırım, Süleyman, HATEMİ, Ali İbrahim, Yildirim, Suleyman, YILMAZ, Umut   +10 more
core   +1 more source

Physiotherapeutic rehabilitation in Behçet Syndrome: a literature survey

O Mundo da Saúde, 2010
Behçet syndrome (BS) is a multi-systemic inflammatory affection of vascular incidence and unknown cause, characterized by recurrent mouth and genital ulcers, uveitis, cutaneous injuries, articulation and neuromuscular incidence.
Maurício Bezerra da Silva, Joyce de Sena Mantovani, Juliana Santos Cruz, Vanessa Simões Del Valhe dos Santos   +3 more
doaj  

Neuro angio Behçet: à propos d’un cas

Avicenna Medical Research
Résumé La maladie de Behçet est une vascularite chronique, multisystémique. L’atteinte thoracique la plus fréquente est l’anévrisme de l’artère pulmonaire. L’atteinte neurologique se présente avec des anomalies caractéristiques à l’imagerie.
H Menia, F Megdoud, F/Z. Lalami, A. Kadi, A Kheliouen, M GHARNAOUT   +5 more
doaj   +1 more source

Patterns of uveitis at a tertiary referral center in Northeastern Iran

Journal of Ophthalmic & Vision Research, 2018
Purpose: To describe the demographic and clinical patterns of patients with uveitis referred to a tertiary center in northeastern Iran. Methods: This cross-sectional retrospective study included 235 patients with uveitis who had been referred to the ...
Seyedeh Maryam Hosseini, Nasser Shoeibi, Raheleh Ebrahimi, Mehdi Ghasemi   +3 more
doaj   +1 more source

An Exploration of the Relationships Between Science Identity and Disabled Identities in Undergraduate Science Students

Science Education, EarlyView.
ABSTRACT Science identity is often conceptualized through constructs such as performance, competence, recognition, and interest, with prior research highlighting the roles of race, gender, and cultural background in shaping students' experiences. However, limited scholarship has examined how disability interacts with science identity in postsecondary ...
Ariel Chasen, Maura Borrego
wiley   +1 more source

Colchicine in Behcet Syndrome: A Longterm Survey of Patients in a Controlled Trial

, 2014
Objective. To test the hypothesis that colchicine use during early disease decreases immunosuppressive use in Behcet syndrome (BS) in the long ...
Ozyazgan, Yilmaz, Hamuryudan, Vedat, Hatemi, Gulen, Mat, Cem, Ugurlu, Serdal, Seyahi, Emire, Yurdakul, Sebahattin, Tascilar, Koray, Yazici, Hasan   +8 more
core   +1 more source

Primary Cutaneous Gamma‐Delta T‐Cell Lymphoma Complicating Long‐Standing Immunosuppressed Dermatomyositis

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Primary cutaneous gamma‐delta T‐cell lymphoma (PCGD‐TCL) is a rare cytotoxic lymphoma with key oncogenic drivers in the JAK/STAT pathway. Also primarily involving the subcutaneous adipose tissue, subcutaneous panniculitis‐like T‐cell lymphoma (SPTCL) is more frequently encountered in scenarios of autoimmune disorders.
Bennett Christie‐Nguyen, Youn H. Kim, David F. Fiorentino, Danielle Tartar, Ryanne Brown, Robert A. Novoa, Kerri E. Rieger   +6 more
wiley   +1 more source