Results 21 to 30 of about 4,852,104 (194)

Budd-Chiari syndrome in a 25-year-old woman with Behçet's disease: a case report and review of the literature

Journal of Medical Case Reports, 2011
Introduction The risk that patients with Behçet's disease will develop thrombotic complications has been previously described. Although it is distributed worldwide, Behçet's disease is rare in the Americas and Europe.
Évora Paulo RB, Matsuda Nilce M, Oikawa Fernando T, Carvalho Daniela T, Yamada Alice T   +4 more
doaj   +1 more source

Additional file 2: of A metagenomic study of the gut microbiome in Behcetâ s disease

, 2018
Supplementary Figures. (PDF 975 kb)
Ye, Zi, Zhang, Ni, Wu, Chunyan, Zhang, Xinyuan, Wang, Qingfeng, Huang, Xinyue, Du, Liping, Cao, Qingfeng, Tang, Jihong, Zhou, Chunjiang, Hou, Shengping, He, Yue, Xu, Qian, Xiong, Xiao, Kijlstra, Aize, Qin, Nan, Yang, Peizeng   +16 more
openaire   +1 more source

0274: Cardiac involvement in Behcet’s disease [PDF]

, 2015
BackgroundBehcet’s disease is a multisystem disorder and classified as « vasculitic syndrome with a wide variety of clinical manifestations. » Cardiac involvement is very rare but can occur with different presentations.ObjectiveTo analyze the clinical ...
Leila, Abid, Ahmed, Tounsi, Sahar, Elaoud, Feten, Frikha, Mourad, Hentati, Zouhir, Bahloul, Samir, Kammoun, Malek, Akrout   +7 more
core   +1 more source

Behçet's Disease (Adamantiades-Behçet's Disease)

Clinical and Developmental Immunology, 2011
Adamantiades-Behçet's disease (ABD) is characterized by starting with oral aphthous ulceration and developing of the systemic involvements. The pathogenesis of ABD is closely correlated with the genetic factors and the triggering factors which acquire ...
Fumio Kaneko, Ari Togashi, Sanae Saito, Hideo Sakuma, Noritaka Oyama, Koichiro Nakamura, Kenji Yokota, Keiji Oguma   +7 more
doaj   +1 more source

Additional file 1: of Predictors of paravalvular aortic regurgitation after surgery for Behcetâ s disease-related severe aortic regurgitation

, 2019
Figure S1. Schematic diagram showing the selection process of the patient population. Figure S2. Kaplan-Meier estimates of freedom from paravalvular leakage (PVL) stratified by satisfaction of the International Study Group (ISG) criteria. Figure S3. Kaplan-Meier estimates of freedom from paravalvular leakage (PVL) in patients who received postoperative
Choi, Hong-Mi, Kim, Hyung-Kwan, Park, Sung-Ji, Lee, Hyun-Jung, Yoon, Yeonyee, Park, Jun-Bean, Kim, Yong-Jin, Cho, Goo-Young, Hwang, In-Chang, Sohn, Dae-Won, Oh, Jae   +10 more
openaire   +1 more source

Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. [PDF]

, 2010
The unparalleled collection of clinical data and biomaterials within the EHDN's REGISTRY can expedite the search for disease modifiers (genetic and environmental) of age at onset and disease progression that could be harnessed for the development of ...
Handley, Olivia J, Landwehrmeyer, G Bernhard, Aileen K Ho, Bisson, Jonathan Ian, Schwenke C, David Craufurd, Dunnett, Stephen B., Handley, Olivia, Investigators of the European Huntington's Disease Network, The, DI MARIA, EMILIO, Craufurd D, Dunnett, SB, Carsten Schwenke, the investigators of the European Huntington's Disease Network, Craufurd, David, Edward Wild, Landwehrmeyer, GB, Busse, Monica, Rosser, Anne Elizabeth, Olivia J Handley, Romano Silvia., Tabrizi SJ, Ho, Aileen K., Wild, E, Landwehrmeyer GB, Craufurd, D, Tabrizi, SJ, Tabrizi, Sarah J., Handley, OJ, Rickards, Hugh, Dunnett, Stephen, Ho, Aileen K, Orth, Michael, Ho, AK, Wild, Edward, Stephen B. Dunnett, Sarah J Tabrizi, Wild, EJ, Landwehrmeyer, G. Bernhard, Naji, Jenny, Landwehrmeyer, G. Bernhard, Wild E, Investigators of the European Huntington's Disease Network, Handley, Olivia J., Orth, M, Ellison-Rose, Lynda, Tabrizi, Sarah J, Price, Kathleen, Ho AK, ABBRUZZESE, GIOVANNI, Schwenke, C, Ho, A, Orth M, Handley OJ, Schwenke, Carsten, Dunnett SB, Dunnett, Stephen B, Michael Orth, G. Bernhard Landwehrmeyer   +59 more
core   +1 more source

Behcet’s Disease; do natural killer cells play a significant role?

Frontiers in Immunology, 2015
Behçet's Disease is a complex inflammatory disease, of unknown aetiology. While disease pathogenesis remains unclear, a strong relationship between Behçet’s Disease and HLA-B*51 has been established over the last 30 years.
Harry ePetrushkin, Md Samiul eHasan, Miles eStanford, Farida eFortune, Graham eWallace   +4 more
doaj   +1 more source

Retractions in Rheumatology: Trends, Causes, and Implications for Research Integrity

Arthritis Care &Research, EarlyView.
Objective We aimed to describe the trends and main reasons for study retraction in rheumatology literature. Methods We reviewed the Retraction Watch database to identify retracted articles in rheumatology. We recorded the main study characteristics, authors’ countries, reasons for retraction, time from publication to retraction, and trends over time ...
Anna Maria Vettori, Michele Iudici
wiley   +1 more source

Efficacy of Adalimumab in a Girl with Refractory Intestinal Behcet’s Disease [PDF]

, 2015
We describe our experience with a juvenile patient who had refractory intestinal Behcet’s disease that responded to adalimumab, a fully humanized antibody against soluble TNF-α and its receptor.
Satoru Nagata, Satoshi Fujikawa, Takayuki Kishi, Mariko Kaji, Hisashi Yamanaka, Takako Miyamae   +5 more
core   +1 more source

Acute myeloid leukemia in a young male patient with Behçet’s disease presenting with febrile neutropenia

Rheumatology, 2019
Behçet’s disease is a multi-systemic vasculitis which is characterized by recurrent oral and genital ulceration with positive pathergy test. These features may also be seen in various hematological malignancies. In patients with leukemia who present with
Ashish Sharma, Mohammad Ali, Shruti Chauhan, Smita Singh, Vivek Arya   +4 more
doaj   +1 more source