Yazar "Akdeniz, S." seçeneğine göre listele

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    Baseline and stimulated thyroid functions in Behcet's disease
    (Blackwell Publishing, 2006) Akdeniz, S.; Colak, S.; Tuzcu, A. K.; Bahceci, M.; Harman, M.
    [Abstract Not Available]
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    Lack of genotype-phenotype correlation for Kindlin-1 mutations in Kindler syndrome and evidence for possible genetic heterogeneity
    (Wiley-Blackwell, 2008) Lai-Cheong, J.; Liu, L.; Taskesen, M.; Akdeniz, S.; Maari, C.; Emanuel, P.; McGrath, J. A.
    [Abstract Not Available]
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    Loxosceles reclusa bite to the eyelid
    (Wichtig Editore, 2008) Keklikci, U.; Akdeniz, S.; Sakalar, Y. B.; Cakmak, S. S.; Unlu, K.
    PURPOSE. The authors report a case of Loxosceles reclusa infestation on the eyelid. METHODS. The specimen collected by swabbing the lesions with gauze was tested by using a venom-specific enzyme-linked immunosorbent assay. Loxosceles venom was detected in specimen. The patient was managed with conservative therapy that included saline compresses and ocular lubrication. RESULTS. The case presented with severe edema and necrosis on the left upper eyelid. On laboratory examination, a significant left shift of white blood cell count was detected. Although residual scar of the eyelid and punctate epitheliopathy on the inferior of cornea was detected, vision was not impaired. CONCLUSIONS. Supportive therapy may be reasonable treatment for Loxosceles reclusa infestation on the eyelids. The presence of venom proteins detected with an enzyme-linked immunosorbent assay technique is beneficial for supporting the diagnosis of Loxosceles envenomatio. (Eur J Ophthalmol 2008; 18: 633-5)
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    Netherton syndrome resulting from a novel homozygous SPINK5 mutation, p.Gln333X, in a Turkish pedigree
    (Wiley-Blackwell, 2011) Lai-Cheong, J.; Fong, K.; Akdeniz, S.; Isi, H.; Taskesen, M.; McGrath, J. A.
    [Abstract Not Available]
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    THE TUMOR NECROSIS FACTOR-A (TNF-A) GENE-308 G/A POLYMORPHISM AND THE TUMOR NECROSIS FACTOR-RELATED APOPTOSIS-INDUCING LIGAND (TRAIL) GENE POLYMORPHISMS IN BEHCET'S DISEASE
    (Diagnosis Press Ltd, 2010) Isi, H.; Erdal, M. E.; Akdeniz, S.; Oral, D.; Ay, O. I.; Tekes, S.; Sula, B.
    Behcet's disease (BD) is a chronic, multisystemic inflammatory disease. The specific etiology of BD remains elusive, but the interaction between infectious-agent exposure and genetic factors may have a role. In this report, we aim to investigate the possible association between pathogenesis of the BD and TNF-alpha gene 308A/G (rs1800629) polymorphism and the TRAIL gene (Arg141His, G422A (rs6557634), Thr209Arg, C626G (rs20575) and Glu228Ala, A683C (rs20576)) polymorphisms in people from southeast of Turkey. The study population consisted of 55 BD patients and 80 healthy subjects. All samples were collected and studied between July 2009 and January 2010. Polymorphisms were detected by polymerase chain reaction restriction fragment length-polymorphism (PCR-RFLP) analysis. The patients and healthy control groups were similar with respect to their ages and sex characteristic. Statistically, there was not significant difference between the BD patients and healthy control groups in terms of TRAIL Arg141His, G422A (rs6557634) polymorphism, TRAIL Thr209Arg, C626G (rs20575), TRAIL Glu228Ala, A683C (rs20576) and TNF-alpha-308 G/A (rs1800629) polymorphisms. We could not detect statistically significant difference between the BD patients and healthy control groups according to TNF-a-308 G/A (rs1800629), TRAIL Arg141His, G422A (rs6557634), TRAIL Thr209Arg, C626G (rs20575) and TRAIL Glu228Ala, A683C (rs20576) gene polymorphism.