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Featured researches published by Murat Sayan.


Journal of Clinical Virology | 2016

Clinical outcomes in children with herpes simplex encephalitis receiving steroid therapy

Hülya Maraş Genç; Emek Uyur Yalçın; Murat Sayan; Asuman Bayhan; Selim Öncel; Emin Sami Arisoy; Bülent Kara

BACKGROUNDnHerpes simplex virus encephalitis (HSE) is a significant cause of morbidity and mortality. Neurologic sequelae are common even after early initiation of acyclovir treatment. The host immune response during HSE can also lead to brain damage. There are an increasing number of reports favoring steroid use in HSE.nnnOBJECTIVESnWe aimed to compare the prognosis of children with HSE with and without steroid therapy.nnnSTUDY DESIGNnWe retrospectively screened our hospital archive from 2009 to 2014 for patients diagnosed with HSE with a positive result for herpes simplex virus polymerase chain reaction in cerebrospinal fluid. Patients ≥1 month and ≤18 years at diagnosis were included in the study. Clinical outcomes in terms of cognitive function, motor function, electroencephalographic findings, seizure frequency, and radiologic findings were compared in patients who received adjuvant steroid therapy with those who did not.nnnRESULTSnSix patients (1 boy, 5 girls; aged 4 months to 10 years) were included. Overall symptom duration before hospital admission was ≤5days. Patients received acyclovir treatment for 21-28days. Three received steroid therapy early during the disease and three patients did not. No adverse effects related to steroids were observed. Follow-up duration was 6 months to 5 years. All patients had radiologic sequelae of encephalitis. Cognition, motor function, and seizure control were better in patients who received steroid therapy.nnnCONCLUSIONSnAdjuvant steroid therapy seems to be effective in decreasing morbidity in children with HSE but the radiologic sequelae were the same in both groups.


Pathology Research and Practice | 2016

Detection of human papillomavirus in esophageal and gastroesophageal junction tumors: A retrospective study by real-time polymerase chain reaction in an instutional experience from Turkey and review of literature.

Düriye Özer Türkay; Çiğdem Vural; Murat Sayan; Yesim Gurbuz

Esophageal cancer is a poor-prognosis malignancy that ranks eighth among all cancer types, and its prevalence shows differences among geographical regions. Although the most important risk factors for esophageal carcinoma are alcohol and smoking, viral infections, particularly HPV infection, are also considered among etiological agents. Our study aims to detect the presence of HPV in esophageal cancers in our patient population and to investigate its correlation with clinico-pathological parameters. We investigated the presence of HPV-DNA by real-time polymerase chain reaction in a total of 52 patients with esophageal cancer. Subtype analysis was performed in positive cases and was correlated with selected clinico-pathological parameters. Five (9.6%) of 52 tumor samples, 3 squamous cell carcinomas (3/33 cases) and 2 adenocarcinomas (2/19 cases), were HPV-DNA-positive. Subtype analysis could be performed in four HPV-DNA-positive cases, of which three were HPV type-39 and 1 was type-16. The Marmara region, where the present study was carried out, is a region with low-moderate risk for esophageal cancer, and the prevalence of HPV-DNA in these tumors is similar to the prevalence of HPV-DNA reported in the literature for regions with similar risk. In conclusion, we detected HPV DNA in a subset of esophageal and gastroesophageal junction tumors. HPV infection may have a role in esophageal carcinogenesis and high-risk HPV subtypes can particularly be considered among risk factors since the prevalence of high risk HPV infection has also been found to be increased in regions with a high risk for esophageal cancer compared to low-moderate risk regions.


International Journal of Infectious Diseases | 2016

Protease Inhibitors Drug Resistance Mutations in Turkish Patients with Chronic Hepatitis C

Elif Sargin Altunok; Murat Sayan; Sila Akhan; Bilgehan Aygen; Orhan Yildiz; Suda Tekin Koruk; Resit Mistik; Nese Demirturk; Onur Ural; Şükran Köse; Aynur Aynioglu; Fatime Korkmaz; Gulden Ersoz; Nazan Tuna; Celal Ayaz; Faruk Karakecili; Derya Keten; Dilara Inan; Saadet Yazici; Safiye Koculu; Taner Yildirmak

BACKGROUNDnDrug resistance development is an expected problem during treatment with protease inhibitors (PIs), this is largely due to the fact that Pls are low-genetic barrier drugs. Resistance-associated variants (RAVs) however may also occur naturally, and prior to treatment with Pls, the clinical impact of this basal resistance remains unknown. In Turkey, there is yet to be an investigation into the hepatitis C (HCV) drug associated resistance to oral antivirals.nnnMATERIALS AND METHODSn178 antiviral-naïve patients infected with HCV genotype 1 were selected from 27 clinical centers of various geographical regions in Turkey and included in the current study. The basal NS3 Pls resistance mutations of these patients were analyzed.nnnRESULTSnIn 33 (18.5%) of the patients included in the study, at least one mutation pattern that can cause drug resistance was identified. The most frequently detected mutation pattern was T54S while R109K was the second most frequently detected. Following a more general examination of the patients studied, telaprevir (TVR) resistance in 27 patients (15.2%), boceprevir (BOC) resistance in 26 (14.6%) patients, simeprevir (SMV) resistance in 11 (6.2%) patients and faldaprevir resistance in 13 (7.3%) patients were detected. Our investigation also revealed that rebound developed in the presence of a Q80K mutation and amongst two V55A mutations following treatment with TVR, while no response to treatment was detected in a patient with a R55K mutation.nnnCONCLUSIONnWe are of the opinion that drug resistance analyses can be beneficial and necessary in revealing which variants are responsible for pre-treatment natural resistance and which mutations are responsible for the viral breakthrough that may develop during the treatment.


Journal of global antimicrobial resistance | 2016

Epidemiological and molecular characteristics of meticillin-resistant Staphylococcus aureus in Turkey: A multicentre study

Devrim Dundar; Ayse Willke; Murat Sayan; Meliha Meric Koc; Özay Arıkan Akan; Bulent Sumerkan; Nese Saltoglu; Akgün Yaman; Celal Ayaz; Iftihar Koksal

The aim of this study was to investigate the epidemiological and molecular features of clinical meticillin-resistant Staphylococcus aureus (MRSA) isolates in Turkey. MRSA isolates were collected from six regions of Turkey. The mecA and nuc genes were detected by PCR. Antimicrobial susceptibilities were determined by the disk diffusion method. Staphylococcal cassette chromosome mec (SCCmec) and staphylococcal protein A (spa) typing were performed by the sequencing method for 270 randomly selected MRSA isolates. The US Centers for Disease Control and Prevention (CDC) definition was used for epidemiological diagnosis of community-associated MRSA (CA-MRSA). Resistance rates of MRSA to ciprofloxacin, gentamicin, clindamycin, erythromycin, rifampicin, trimethoprim/sulfamethoxazole and tetracycline were 93.4%, 81.2%, 38.5%, 57.8%, 93.9%, 1.1% and 93.1%, respectively. The most frequent SCCmec type was SCCmec III (91.1%). SCCmec type IV was found in 5.2% of the isolates. The most frequent spa type was t030 (81.1%). Five isolates were CA-MRSA if only the epidemiological definition was used (5/725; 0.7%). Two isolates were defined as CA-MRSA both by epidemiological features and SCCmec typing (2/270; 0.7%). Of 14 SCCmec type IV isolates, 12 were not defined as CA-MRSA by epidemiological features. In conclusion, this is the most comprehensive multicentre study in Turkey investigating MRSA using both epidemiological and genotypic features. The CA-MRSA rate is low in Turkey. Combined use of epidemiological and genotypic methods is the most accurate approach for the diagnosis of CA-MRSA.


Future Virology | 2013

Investigation of adipogenic effects of human adenovirus serotypes 36 and 5 in a Colo-320 cell line

Tamer Sanlidag; Sinem Akcali; Seda Vatansever; Candan Çiçek; Murat Sayan; Elcin Kal Cakmakliogullari; Pinar Taskiran Sen


Mikrobiyoloji Bulteni | 2012

Molecular typing of adenoviruses isolated from clinical specimens by PCR and DNA sequencing methods

Candan Çiçek; Tamer Sanlidag; Sinem Akcali; Murat Sayan; Yalaz M; Metin Dy


Future Virology | 2018

Could resistant and escape variants of hepatitis B virus be a problem in the future

Müge Özgüler; Murat Sayan


Mikrobiyoloji Bulteni | 2017

Genotip 1 ile Enfekte Kronik Hepatit C Hastalarında NS3 İnhibitörü İlaçların Direnç Mutasyonlarının Belirlenmesi

Tamer Şanlidağ; Murat Sayan; Sinem Akcali; Elmas Kasap; Tahir Buran; Arıkan A


Journal of Biotechnology | 2017

Performance characteristics and comparison of DxN Veris system versus Qiagen PCR kit for Hepatitis B virus quantification

Murat Sayan; Arıkan A; Tamer Sanlidag


Journal of Biotechnology | 2017

Determination of NS3 inhibitors drug resistance mutations in chronic Hepatitis C patients infected with genotype 1

Tamer Sanlidag; Murat Sayan; Si̇nem Akcali; Elmas Kasap; Tahi̇r Buran; Arıkan A

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