Yazar "Aylanc, H." seçeneğine göre listele

Listeleniyor 1 - 3 / 3
  • [ X ]
    Öğe
    Does topical use of autologous serum help to reduce post-tonsillectomy morbidity? A prospective, controlled preliminary study
    (Cambridge Univ Press, 2016) Kara, M.; Erdogan, H.; Altinisik, H. B.; Aylanc, H.; Guclu, O.; Derekoy, F. S.
    Background: To evaluate the effects of autologous serum usage on throat pain, haemorrhage and tonsillar fossa epithelisation in patients after tonsillectomy. Methods: Thirty-two patients (aged 4-15 years) were included in the study. Tonsillectomy was performed and autologous serum was administered topically to the right tonsillar fossa during the operation, and at 8 and 24 hours post-operatively. The left side served as the control. A visual analogue scale was used to record the patient's pain every day. Each patient's oropharynx was observed on the 5th and 10th post-operative days to examine bleeding and epithelisation. Results: The pain scores for the side administered autologous serum were significantly lower than those for the control side, on the night following the operation and on the 1st, 2nd, 5th and 6th post-operative days. Tonsillar fossa epithelisation was significantly accelerated on the study side compared with the control side on the 5th and 10th post-operative days. Conclusion: In tonsillectomy patients, topically administered autologous serum contributed to throat pain relief and tonsillar fossa epithelisation during the post-operative period.
  • [ X ]
    Öğe
    Knowledge and attitudes regarding drug allergy among residents and interns in Tracia region of Turkey; a multicenter study
    (Wiley, 2019) Ozdemir, Gokmirza P.; Kizilca, O.; Aylanc, H.; Celik, V; Beken, B.; Yazicioglu, M.; Sut, N.
    [Anstract Not Available]
  • [ X ]
    Öğe
    THE MEFV GENE PATHOGENIC VARIANTS AND PHENOTYPE-GENOTYPE CORRELATION IN CHILDREN WITH FAMILIAL MEDITERRANEAN FEVER IN THE CANAKKALE POPULATION
    (Macedonian Acad Sciences Arts, 2016) Battal, F.; Sılan, Fatma; Topaloglu, N.; Aylanc, H.; Yildirim, S.; Binnetoglu, Koksal F.; Tekin, M.
    The aim of the current study was to determine the frequency of the Mediterranean fever (MEFV) gene pathogenic variants in 60 children diagnosed with familial Mediterranean fever (FMF) and to compare the phenotype-genotype correlation. Genomic DNA was isolated by the spin-column method from peripheral blood samples (collected in vacutainers containing EDTA) and buccal smears. The MEFV gene profiles for the current FMF cohort were genotyped by pyrosequencing and direct Sanger sequencing techniques for the target pathogenic variants. The most prominent clinical symptoms were abdominal pain (53.4%), fever (23.4%) and arthritis (23.3%). Eighteen different pathogenic variants were identified and the most frequent were p. Met694Val (20.0%), p. Glu148Gln (13.3%), p. Met680 Ile (11.7%) and p. Arg202Gln (11.7%). Abdominal pain, fever and arthritis were the most common presenting clinical characteristics. Results showed that not only clinical characteristics, but also genotyping of the MEFV gene is needed to establish the correct diagnosis of FMF in children and other family members.