Search Results - "CETIN, Timur"

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    Chronically Restricted Sleep Leads to Depression-Like Changes in Neurotransmitter Receptor Sensitivity and Neuroendocrine Stress Reactivity in Rats by NOVATI, Arianna, ROMAN, Viktor, CETIN, Timur, HAGEWOUD, Roelina, DEN BOER, Johan A, LUITEN, Paul G. M, MEERLO, Peter

    Published in Sleep (New York, N.Y.) (01-11-2008)
    “…Frequently disrupted and restricted sleep is a common problem for many people in our Western society. In the long run, insufficient sleep may have…”
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    A virtual reality simulation of a novel way to illuminate the surgical field - A feasibility study on the use of automated lighting systems in the operating theatre by Cetin, Timur, Mühlenbrock, Andre, Zachmann, Gabriel, Weber, Verena, Weyhe, Dirk, Uslar, Verena

    Published in Frontiers in surgery (02-03-2023)
    “…Surgical lighting systems have to be re-adjusted manually during surgery by the medical personnel. While some authors suggest that interaction with a surgical…”
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    Investigating the attentional focus to workplace-related soundscapes in a complex audio-visual-motor task using EEG by Rosenkranz, Marc, Cetin, Timur, Uslar, Verena N, Bleichner, Martin G

    Published in Frontiers in neuroergonomics (02-02-2023)
    “…In demanding work situations (e.g., during a surgery), the processing of complex soundscapes varies over time and can be a burden for medical personnel. Here…”
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    High TUBB2A expression in childhood T‐ALL is correlated with the clinical outcome by Khodzhaev, Khusan, Ng, Ozden Hatirnaz, Tugcu, Deniz, Erbilgin, Yucel, Ng, Yuk Yin, Celkan, Tiraje, Timur, Cetin, Karakas, Zeynep, Ozdemir, Gul Nihal, Yıldırmak, Yıldız, Sayitoglu, Muge

    “…Introduction Microtubules are polymers that perform functions such as mitosis, intracellular transport, cell morphology, and ciliary and flagellar motility…”
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    Case Report: How an Iliac Vein Lesion During Totally Endoscopic Preperitoneal Repair of an Inguinal Hernia Can Be Safely Managed by Tabriz, Navid, Uslar, Verena Nicole, Cetin, Timur, Marth, Andreas, Weyhe, Dirk

    Published in Frontiers in surgery (12-08-2021)
    “…Inguinal hernia repair is a common surgical procedure with an acceptably low complication rate. However, complications with potentially life-threating…”
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    Chylous ascites after lymphadenectomy in a Wilms` tumor patient by Yörük, Mustafa Asım, Erat-Nergiz, Meryem, Timur, Çetin, Canbolat-Ayhan, Aylin, Ergüven, Müferet

    Published in Turkish journal of pediatrics (2018)
    “…Yörük MA, Erat-Nergiz M, Timur Ç, Canbolat-Ayhan A, Ergüven M. Chylous ascites after lymphadenectomy in a Wilms` tumor patient. Turk J Pediatr 2018; 60:…”
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    Dopamine in the orbitofrontal cortex regulates operant responding under a progressive ratio of reinforcement in rats by Cetin, Timur, Freudenberg, Florian, Füchtemeier, Martina, Koch, Michael

    Published in Neuroscience letters (11-11-2004)
    “…Prefrontocortical dopamine (DA) plays an essential role in the regulation of cognitive functions and behavior. The orbitofrontal cortex (OFC) receives a…”
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    As a Rare Site of Invasive Fungal Infection, Chronic Granulomatous Aspergillus Synovitis: A Case Report by Canbolat Ayhan, Aylin, Ozkan, Korhan, Timur, Cetin, Aktaş, Birol, Ceyran, Ayse Bahar

    “…Aspergillus can causes invasive disease of various organs especially in patients with weakened immune systems. Aspergillus synovitis and arthritis are uncommon…”
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    Spontaneous Intestinal Perforation : An Atypical Presentation of Neutropenic Enterocolitis—A Case Report by Canbolat Ayhan, Aylin, Timur, Cetin, Bocu, Ersin, Gulcin, Neslihan

    Published in Case reports in hematology (01-01-2014)
    “…Background. Neutropenic enterocolitis is one of the most common gastrointestinal complications seen in patients who are receiving chemotherapy for leukemia…”
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    Myeloid Sarcoma Presenting with Leukemoid Reaction in a Child Treated for Acute Lymphoblastic Leukemia by Zemheri, Ebru, Sonmez, Seyma, Timur, Cetin, Canbolat Ayhan, Aylin, Yoruk, Asım

    Published in Case reports in hematology (01-01-2014)
    “…Background. Myeloid sarcoma is an extramedullary neoplasm of immature myeloid cells. Our study reports a presentation of myeloid sarcoma which presented with…”
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    INVESTIGATION OF SALİVARY MIR-9 AND SERUM CIP2A LEVELS IN FANCONI ANEMIA PATIENTS AT HIGH RISK OF DEVELOPING ORAL SQUAMOUS CELL CARCINOMA by Zişan Asal Kılıç, Çetin Timur, Tülin Tiraje Celkan, Şahin Öğreden, Nevin Yalman

    Published in Hematology, Transfusion and Cell Therapy (01-10-2023)
    “…Objective: Fanconi anemia (FA) is a rare bone marrow failure syndrome caused by mutations in DNA repair genes, and the risk of developing Oral Squamous Cell…”
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    Investigation of Possible Sources of Electrodermal Activity in Surgical Personnel to Assess Workplace Stress Levels by Schlender, Merle, Uslar, Verena, Uppenkamp, Stefan, Tabriz, Navid, Weyhe, Dirk, Cetin, Timur

    Published in Sensors (Basel, Switzerland) (08-11-2024)
    “…Objective: The aim of this study was to evaluate alternative measurement points to assess stress levels during surgery, given that taking electrodermal…”
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    RARE COAGULATION DISORDERS. Retrospective analyses of 156 patients in TURKEY by Fisgin, Tunc, Balkan, Can, Celkan, Tiraje, Kilinc, Yurdanur, Turker, Meral, Timur, Cetin, Gursel, Turkiz, Kurekci, Emin, Duru, Feride, Kupesiz, Alphan, Olcay, Lale, Yilmaz, Sebnem, Ozgen, Unsal, Unuvar, Aysegul

    Published in Turkish journal of haematology (01-03-2012)
    “…OBJECTIVE: We evaluated the clinical findings, laboratory data, management, and outcome of children with rare coagulation deficiencies (RCDs) diagnosed in…”
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    Use of a High-Purity Factor X Concentrate in Turkish Subjects with Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study by Öner, Ahmet F, Celkan, Tiraje, Timur, Çetin, Norton, Miranda, Kavaklı, Kaan

    Published in Turkish journal of haematology (25-05-2018)
    “…Hereditary factor X (FX) deficiency is a rare bleeding disorder more prevalent in countries with high rates of consanguineous marriage. In a prospective,…”
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    Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective by Karakaş, Zeynep, Koç, Begüm, Temurhan, Sonay, Elgün, Tuğba, Karaman, Serap, Asker, Gamze, Gençay, Genco, Timur, Çetin, Yıldırmak, Zeynep Yıldız, Celkan, Tiraje, Devecioğlu, Ömer, Aydın, Filiz

    Published in Turkish journal of haematology (01-12-2015)
    “…Alpha thalassemia syndromes are caused by mutations on one or more of the four α-globin genes. Mutations could be either more commonly deletional or…”
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