Bölüm "Kulak Burun Boğaz" Cerrahi Tıp Bilimleri Bölümü Makale Koleksiyonu için listeleme
Toplam kayıt 44, listelenen: 1-20
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A Rare Location of Angiofibroma in the Inferior Turbinate in Young Woman
(2015)Introduction Juvenile nasopharyngeal angiofibroma is a rare benign neoplasm in the nasopharynx. The tumor tends to be locally aggressive and is typically seen in adolescent boys. Extranasopharyngeal angiofibromas have been ... -
An Evaluation of the Quality of Life in Patients with Tracheostomy
(Professional Medical Publications, 2010)Objective: To evaluate the quality of life in patients with tracheostomy. Methodology: All the patients, who have had tracheostomy operations between 1998-2009 at a University Hospital, Turkey, constitute the population ... -
Association of Adenoid Surface Biofilm Formation and Chronic Otitis Media with Effusion
(Amer Medical Assoc, 2010)Objectives: To investigate bacterial biofilm formation on the adenoid surface of pediatric patients undergoing adenoidectomy and to reveal whether this formation is associated with chronic otitis media with effusion (COME). ... -
Association of Skin Thickness with Alar Base Reduction in Patients Undergoing Lateral Crural Repositioning and Strut Grafting
(Amer Medical Assoc, 2017)IMPORTANCE Knowing the operation plan is important for rhinoplasty surgeons to prevent unpredictable results. OBJECTIVES To investigate the frequency of alar base resection in patients with different skin thickness who ... -
Association of Ugrp2 Gene Polymorphisms with Adenoid Hypertrophy in the Pediatric Population
(Assoc Brasileira Otorrinolaringologia & Cirurgia Cervicofacial, 2018)Introduction: Adenoid hypertrophy is a condition that presents itself as the chronic enlargement of adenoid tissues; it is frequently observed in the pediatric population. The Ugrp2 gene, a member of the secretoglobin ... -
Auditory Evoked Potentials in a Newborn Wistar Rat Model of Hyperbilirubinemia
(Assoc Brasileira Otorrinolaringologia & Cirurgia Cervicofacial, 2016)Introduction: Hyperbilirubinemia is a common health problem in newborns. Its effects can be different according to the level and duration of the hyperbilirubinemia. The toxic effect of bilirubin on the auditory system can ... -
Classification And Current Management Of Inner Ear Malformations
(2017)Morphologically congenital sensorineural hearing loss can be investigated under two categories. The majority of congenital hearing loss causes (80%) are membranous malformations. Here, the pathology involves inner ear hair ... -
Clear Otorrhea: A Case Of Munchausen Syndrome In A Pediatric Patient
(2008)This paper reports a case of Munchausen syndrome in a pediatric patient. An 11-year-old girl presented with the complaint of clear fluid otorrhea. She underwent numerous investigations with deception of the physicians. The ... -
Cochlear Implantation In Neurobrucellosis
(Aves, 2016)Background: Neurobrucellosis is a disease consisting of a wide spectrum of complications such as peripheral neuropathy, cranial nerve involvement, ataxia, meningeal irritation, paraplegia, seizures, coma, and even death. ... -
Comparison Of Hearing Screening Protocols For Universal Newborn Hearing Screening In Turkey
(Aves, 2010)Objective: Congenital hearing loss is one of the most common major abnormalities present at birth. Early diagnose is very important. In this study a comparison of five different newborn hearing screening protocols are made ... -
Comparison Of Voice And Swallowing Parameters After Endoscopic Total And Partial Arytenoidectomy For Bilateral Abductor Vocal Fold Paralysis A Randomized Trial
(Amer Medical Assoc, 2013)IMPORTANCE Total arytenoidectomy is claimed to increase risk of aspiration and cause more voice loss than other operations performed for bilateral abductor vocal fold paralysis (BVFP). However, objective evidence for such ... -
Complete Labyrinthine Aplasia: Clinical And Radiologic Findings With Review Of The Literature
(Amer Soc Neuroradiology, 2009)BACKGROUND AND PURPOSE: Complete labyrinthine aplasia (CLA), also referred to as Michel aplasia, is a severe congenital anomaly of the inner ear, defined by the complete absence of inner ear structures. The purpose of this ... -
Congenital Laryngeal Cyst: A Rare Cause Of Polyhydramnios
(2013)Congenital laryngeal cyst is a rare cause of airway obstruction that may require urgent diagnosis and treatment. We report a case of a neonate having history of polyhydramnios and severe respiratory distress at birth. A ... -
Does Age Affect The Size of Metastatic Lymph Nodes in Head and Neck Cancer?
(Akad Doktorlar Yayınevi, 2013)The aim of the study was to determine if age plays a role in the size of metastatic lymph nodes in elderly patients with squamous cell carcinoma of the head and neck (HNSCC). In 180 HNSCC patients with metastatic lymph ... -
Effects Of Intrauterine And Extrauterine Gsm-Like Radiofrequency On Distortion Product Otoacoustic Emissions In Infant Female Rabbits
(Aves, 2009)Objective: We investigated the effects of 1,800 MHz GSM-like Radiofrequency (RF) on the cochlear functions of female infant rabbits by Distortion Product Otoacoustic Emission (DPOAE) recordings upon intrauterine (IU) and/or ... -
Management of Acquired Atresia of the External Auditory Canal
(Aves, 2015)OBJECTIVE: The aim was to evaluate surgical techniques and their relationship to postoperative success rate and hearing outcomes in acquired atresia of the external auditory canal. MATERIALS and METHODS: In this article, ... -
Novel Domain-Specific Pou3F4 Mutations Are Associated With X-Linked Deafness: Examples From Different Populations
(2015)Background Mutations in the POU3F4 gene cause X-linked deafness type 3 (DFN3), which is characterized by inner ear anomalies. Methods Three Turkish, one Ecuadorian, and one Nigerian families were included based on either ... -
Novel Pathogenic Variants Underlie Slc26A4-Related Hearing Loss In A Multiethnic Cohort
(Elsevier Ireland Ltd, 2017)Objectives: The genetics of sensorineural hearing loss is characterized by a high degree of heterogeneity. Despite this heterogeneity, DNA variants found within SLC26A4 have been reported to be the second most common ...