Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Fügen Ersoy"'
Autor:
Ilhan Tezcan, Burcin B Ozdag, Murat Irkec, Ozden Sanal, Fügen Ersoy, Lutfiye Mesci, Banu Bozkurt, Umut Arslan
Publikováno v:
Clinical & Experimental Ophthalmology. 40:e156-e162
Background: Tumour necrosis factor-alpha (TNF-α) is an important proinflammatory cytokine driving axonal degeneration and retinal ganglion cell apoptosis in glaucoma. The aim of the study was to evaluate the association of TNF-α -308 G/A and -238 G
Autor:
Fügen Ersoy, Mehmet Köse, Ayse Tana Aslan, Nazan Cobanoglu, Nural Kiper, Ebru Yalcin, Sevgi Pekcan, Cagman Tan, Ugur Ozcelik, Deniz Dogru
Publikováno v:
Parasitology Research. 106:795-800
Hydatid disease (HD) is a parasitosis caused by Echinococcus granulosus, which is still an important health problem worldwide, and our country is an endemic region for HD. There is little information regarding the role of human leucocyte antigen (HLA
Publikováno v:
Journal of Clinical and Analytical Medicine, Vol 6, Iss 152, Pp 261-266 (2016)
WOS: 000215591800002 Primary antibody deficiency (common variable immunodeficiency, Hyper IgM, X-linked agammaglobulinemia and selective Ig A deficiency) is a group of heterogeneous diseases characterized by defective antibody production. In primary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7732d7c47dc924fcf451a7fde85f2d2
https://hdl.handle.net/20.500.12605/8246
https://hdl.handle.net/20.500.12605/8246
Long-term survival in severe combined immune deficiency: The role of persistent maternal engraftment
Autor:
Fügen Ersoy, Francois Le Deist, Tuba Turul, Geneviève de Saint Basile, S. Caillat-Zucmann, Ozden Sanal, Ilhan Tezcan, Duygu Uckan, Sevim Balci, Marguerite Prieur, Gönül Hiçsönmez
Publikováno v:
The Journal of Pediatrics. 146:137-140
Two siblings with severe combined immune deficiency, one with maternal engraftment and detectable immunologic functions who was alive at the age of 8 years are presented. Both patients had the same JAK3 gene mutation, suggesting that maternal engraft
Publikováno v:
Journal of Clinical Immunology. 24:411-417
Immunodeficiency is a characteristic feature of ataxia-telangiectasia (A-T). Humoral immunodeficiency generally consists of hypogammaglobulinemia and impaired antibody response to bacterial and viral antigens. We previously observed defective antibod
Autor:
Geneviève de Saint Basile, Gaël Ménasché, Aytemiz Gurgey, Izzet Berkel, Ayse Metin, Fügen Ersoy, Ilhan Tezcan, Ozden Sanal, Leman Yel
Publikováno v:
Journal of Clinical Immunology. 22:237-243
Griscelli disease is a rare autosomal recessive disorder characterized by diffuse pigmentary dilution and occurrence of acute phases of uncontrolled lymphocyte and macrophage activation, so-called “hemophagocytic syndrome” (HS) that leads to deat
Autor:
Yves Levy, Alain Fischer, Alessandro Plebani, Ozden Sanal, Frederic Geissmann, Ilhan Tezcan, Kazuo Kinoshita, Masamichi Muramatsu, Anne Durandy, Hülya Kayserili, Nicole Brousse, Monique Forveille, Fügen Ersoy, Patrick Revy, Dufourcq-Lagelouse R, Alberto G. Ugazio, Nadia Catalan, Taro Muto, Tasuku Honjo, Luigi D. Notarangelo, Andrew R. Gennery
Publikováno v:
Cell. 102:565-575
The activation-induced cytidine deaminase (AID) gene, specifically expressed in germinal center B cells in mice, is a member of the cytidine deaminase family. We herein report mutations in the human counterpart of AID in patients with the autosomal r
Autor:
Dario Campana, Lisa Rapalus, Mary Ellen Conley, Fügen Ersoy, Elaine Coustan-Smith, Yoshiyuki Minegishi
Publikováno v:
Journal of Clinical Investigation. 104:1115-1121
Mutations in Btk, mu heavy chain, or the surrogate light chain account for 85-90% of patients with early onset hypogammaglobulinemia and absent B cells. The nature of the defect in the remaining patients is unknown. We screened 25 such patients for m
Autor:
Ozden Sanal, Leman Yel, Fatma Gumruk, Gülten Seçmeer, Fügen Ersoy, Gulten Turkkani, Ilhan Tezcan, Ateş Kara
Publikováno v:
Pediatric Infectious Disease Journal. 26:366-368
Interleukin-12 receptor beta-1 (IL-12Rbeta1) defect is generally associated with selective susceptibility to weakly pathogenic mycobacteria and Salmonella species. Patients rarely experience infections caused by other organisms. We report a 5-year-ol
Publikováno v:
American Journal of Rhinology. 10:383-386
We report on a 3 month-old female patient having leukocyte adhesion deficiency (LAD) of severe phenotype presenting with perforation of the nasal septum and ulceration on the right ala nasi. Laboratory investigations revealed marked leukocytosis, def