Search Results - "Gungor, Gulay"

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  1. 1

    Morphological Features of the Coccyx in the Turkish Population and Interrelationships Among the Parameters: A Computerized Tomography-Based Analysis by Guneri, Bulent, Gungor, Gulay

    Published in Curēus (Palo Alto, CA) (18-11-2021)
    “…Introduction The coccyx is well-known to be a highly variable structure considering its morphology. To our knowledge, the relationship between the coccygeal…”
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    Interpretation of thyroid glands in a group of healthy children: real-time ultrasonography elastography study by Yurttutan, Nursel, Gungor, Gulay, Bilal, Nagihan, Kizildag, Betul, Baykara, Murat, Sarica, Mehmet Akif

    “…This study aimed to determine the strain index (SI) of normal thyroid parenchyma in a group of healthy children, using ultrasound elastography (USE). The…”
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    The relationship between tinnitus and vascular anomalies on temporal bone CT scan: a retrospective case control study by Kizildag, Betul, Bilal, Nagihan, Yurttutan, Nursel, Sarica, Mehmet Akif, Gungor, Gulay, Baykara, Murat

    “…Introduction Tinnitus is a common symptom in which etiology is unclear in a group of patients. Some of anatomic or vascular variations diagnosed on temporal…”
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    Evaluation of Parotid Glands With Real‐time Ultrasound Elastography in Children by Gungor, Gulay, Yurttan, Nursel, Bilal, Nagihan, Menzicioglu, Mehmet Sait, Duymus, Mahmut, Avcu, Serhat, Citil, Serdal

    Published in Journal of ultrasound in medicine (01-03-2016)
    “…Objectives The aim of this study was to determine the strain index for parotid glands in children by using ultrasound elastography. Methods In this prospective…”
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    Ultrasound Elastography Evaluations in Patient Populations With Various Kidney Diseases by Gungor, Ozkan, Guzel, Fatma Betul, Sarica, Mehmet Akif, Gungor, Gulay, Ganidagli, Berivan, Yurttutan, Nursel, Gorgel, Ahmet Fazil, Altunoren, Orcun

    Published in Ultrasound quarterly (01-06-2019)
    “…ABSTRACTRenal elastography is an ultrasonographic method that has been recently found to provide information on renal functions and fibrosis. In this study, we…”
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    The comparison of resistivity index and strain index values in the ultrasonographic evaluation of chronic kidney disease by Menzilcioglu, Mehmet Sait, Duymus, Mahmut, Citil, Serdal, Gungor, Gulay, Saglam, Mustafa, Gungor, Ozkan, Boysan, Serife Nur, Sarıca, Akif, Avcu, Serhat

    Published in Radiologia medica (01-09-2016)
    “…Objectives Chronic kidney disease (CKD) is a disorder progressing to end-stage kidney failure. Early diagnosis and treatment are important for medical care…”
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    The effect of obstructive sleep apnea syndrome and hypothyroidism to intima-media thickness of carotid artery by Bozkus, Fulsen, Dikmen, Nursel, Güngör, Gülay, Samur, Anıl

    Published in Sleep & breathing (01-03-2017)
    “…Aim Obstructive sleep apnea syndrome (OSAS) is a common disorder and in subjects with OSAS the prevalence of hypothyroidism is approximately 1.2–11 %. The…”
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    A Fatal Complication: Intestinal Perforation Secondary to Migration of a Biliary Stent by Güngör, Gülay, Okur, Nazan

    Published in Polish journal of radiology (17-04-2016)
    “…Stent insertion is widely performed to restore biliary drainage in hepatic, biliary, and pancreatic obstructive conditions. Intestinal perforation due to the…”
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    Idiopathic Unilateral Paralysis of the Palate in a Youth by Güngör, Olcay, Kirik, Serkan, Işikay, Sedat, Güngör, Gülay, Bilal, Nagihan

    Published in Pediatric emergency care (01-06-2018)
    “…ABSTRACTUnilateral isolated paralysis of the soft palate is a rare clinical entity that is associated with rhinolalia and the flow of nasal fluids from the…”
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    Vanishing white matter disease with different faces by Güngör, Gülay, Güngör, Olcay, Çakmaklı, Seda, Maraş Genç, Hülya, İnce, Hülya, Yeşil, Gözde, Dilber, Cengiz, Aydın, Kürşad

    Published in Child's nervous system (01-02-2020)
    “…Purpose The goal of this study was to better understand vanishing white matter (VWM) disease, which is one of the most common hereditary white matter…”
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  12. 12

    Acute Mercury Poisoning in a Group of School Children by Güngör, Olcay, Özkaya, Ahmet Kağan, Kirik, Serkan, Dalkiran, Tahir, Güngör, Gülay, Işikay, Sedat, Davutoğlu, Mehmet, Dilber, Cengiz

    Published in Pediatric emergency care (01-10-2019)
    “…OBJECTIVEElemental mercury is a toxic liquid element that is used widely in the home, medicine, agriculture, and industry. It is readily vaporized and inhaled…”
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    Uncinate Process Variations and Their Relationship with Ostiomeatal Complex: A Pictorial Essay of Multidedector Computed Tomography (MDCT) Findings by Güngör, Gülay, Okur, Nazan, Okur, Erdoğan

    Published in Polish journal of radiology (20-04-2016)
    “…The ostiomeatal complex (OMC) is a key area for the drainage and ventilation of the paranasal sinuses. Stenosis created by inflammation and anatomic variations…”
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    A compound heterozygous EARS2 mutation associated with mild leukoencephalopathy with thalamus and brainstem involvement and high lactate (LTBL) by Güngör, Olcay, Özkaya, Ahmet Kağan, Şahin, Yavuz, Güngör, Gülay, Dilber, Cengiz, Aydın, Kürşad

    Published in Brain & development (Tokyo. 1979) (01-10-2016)
    “…Abstract Mitochondrial glutamyl-tRNA synthetase is a major component of protein biosynthesis that loads tRNAs with cognate amino acids. Mutations in the gene…”
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    A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis by Sahin, Yavuz, Güngör, Olcay, Ayaz, Akif, Güngör, Gülay, Sahin, Bedia, Yaykasli, Kursad, Ceylaner, Serdar

    Published in Brain & development (Tokyo. 1979) (01-02-2017)
    “…Abstract Hereditary congenital facial paresis (HCFP) is characterized by isolated dysfunction of the facial nerve (CN VII) due to congenital cranial…”
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    Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy by Sahin, Yavuz, Güngör, Olcay, Gormez, Zeliha, Demirci, Huseyin, Ergüner, Bekir, Güngör, Gülay, Dilber, Cengiz

    Published in Acta neurologica Belgica (01-03-2017)
    “…Neuronal ceroid lipofuscinosis (NCL), one of the most common neurodegenerative childhood-onset disorders, is characterized by autosomal-recessive inheritance,…”
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    Novel mutation in SUCLA2 identified on sequencing analysis by Güngör, Olcay, Özkaya, Ahmet Kağan, Güngör, Gülay, Karaer, Kadri, Dilber, Cengiz, Aydin, Kürşad

    Published in Pediatrics international (01-07-2016)
    “…Succinate‐CoA ligase, ADP‐forming, beta subunit (SUCLA2)‐related mitochondrial DNA depletion syndrome is caused by mutations affecting the ADP‐using isoform of…”
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