Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Faisal Fayyad"'
Publikováno v:
RETINAL Cases & Brief Reports. 12:291-293
Purpose To report an association between a Stage 4 full-thickness macular hole and focal choroidal excavation. Methods Case report. Results A 46-year-old male patient with high myopia was referred for macular hole surgery and found to have an associa
Autor:
Gerrit R. J. Melles, Marieke Bruinsma, Rajvardhan Azad, Johannes Frank, Jerzy Nawrocki, Peter Szurman, Hein Van Wijck, Essam Alharthi, R.A. Bejjani, Marco Mura, Dan Bourla, Charbel Fahed, Marc Veckeneer, Brahim Bouassida, Kelvin Rivett, Gabor B. Scharioth, David Wong, Enrico Bertelli, Ian Y. H. Wong, Faisal Fayyad, Silke Oellerich, Ziad F. Bashshur, Dmitry O. Shkvorchenko, Andreas Mohr, Iñigo Corcóstegui Crespo
Publikováno v:
Università degli studi di Ferrara-IRIS
Acta ophthalmologica, 92(4), 339-344. Copenhagen Scriptor
Acta ophthalmologica, 92(4), 339-344. Copenhagen Scriptor
Purpose: To evaluate the feasibility of two novel ‘heavy’ dye solutions for staining the internal limiting membrane (ILM) and epiretinal membranes (ERMs), without the need for a prior fluid-air exchange, during macular surgery. Methods: In this p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aabcacaa809c06858a5108c55abb462
http://hdl.handle.net/11392/2481937
http://hdl.handle.net/11392/2481937
Autor:
David H. Verity, Graham R. Wallace, E Kondeatis, Wafa Madanat, H Zureikat, C. A. Kanawati, J. E. Marr, Robert Vaughan, Faisal Fayyad, Miles Stanford
Publikováno v:
European Journal of Immunogenetics. 27:73-76
Intercellular adhesion molecule-1 (ICAM-1) gene polymorphisms have been implicated in the susceptibility to inflammatory diseases, including multiple sclerosis and inflammatory bowel disease. The expression of both soluble and tissue ICAM-1 is increa
Autor:
Miles Stanford, J. E. Marr, G R Wallace, Wafa Madanat, D H Verity, Faisal Fayyad, C A Kanawati, Robert Vaughan, H Zureikat, E. Kondeatis
Publikováno v:
Tissue Antigens. 54:264-272
The role of HLA-B*51 and other major histocompatibility complex (MHC) genes in Behcet's disease (BD) remains unknown. We have performed HLA and tumour necrosis factor (TNF) polymorphism analysis in BD and evaluated their contribution to ocular diseas
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 0306477572
Symptomatic inflammatory bowel disease is not common in pts with BD from Jordan. Endoscopy must be performed in BD pts with GI symptoms.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29964856dd0b05fcf6fa0976ad624079
https://doi.org/10.1007/0-306-48382-3_92
https://doi.org/10.1007/0-306-48382-3_92
Publikováno v:
Advances in experimental medicine and biology. 528
Autor:
C.A Kanawati, D.H Verity, E Kondeatis, R.W Vaughan, Faisal Fayyad, M.R Stanford, Wafa Madanat, I Ayesh, H Zureikat, G.R Wallace
Publikováno v:
American journal of ophthalmology. 128(3)
PURPOSE: Behcet disease is a systemic disease of young adults characterized by venous occlusion in both the deep venous and retinal circulations. In severe ocular disease, blindness may occur despite immunosuppressive treatment. The most common inher