Search Results - "Bayazit, Yildirim A."

Significance of serotonin transporter gene polymorphism in tinnitus by Deniz, Murat, Bayazit, Yildirim A, Celenk, Fatih, Karabulut, Hayriye, Yilmaz, Akin, Gunduz, Bulent, Saridogan, Cagil, Dagli, Muharrerm, Erdal, Emin, Menevse, Adnan

“…To assess the role of serotonin transporter gene (SLC6A4) polymorphism in tinnitus. Fifty-four consecutive patients experiencing subjective tinnitus and 174…”
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Does MESNA application make sense in chronic otitis media surgery? by Kalcioglu, M. Tayyar, MD, Bayazit, Yildirim A., MD

“…[...]from a practical point of view and based on our observation MESNA seems to help dissection of the squamous epithelium…”
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Utilizing Ethnic-Specific Differences in Minor Allele Frequency to Recategorize Reported Pathogenic Deafness Variants by Shearer, A. Eliot, Eppsteiner, Robert W., Booth, Kevin T., Ephraim, Sean S., Gurrola, José, Simpson, Allen, Black-Ziegelbein, E. Ann, Joshi, Swati, Ravi, Harini, Giuffre, Angelica C., Happe, Scott, Hildebrand, Michael S., Azaiez, Hela, Bayazit, Yildirim A., Erdal, Mehmet Emin, Lopez-Escamez, Jose A., Gazquez, Irene, Tamayo, Marta L., Gelvez, Nancy Y., Leal, Greizy Lopez, Jalas, Chaim, Ekstein, Josef, Yang, Tao, Usami, Shin-ichi, Kahrizi, Kimia, Bazazzadegan, Niloofar, Najmabadi, Hossein, Scheetz, Todd E., Braun, Terry A., Casavant, Thomas L., LeProust, Emily M., Smith, Richard J.H.

“…Ethnic-specific differences in minor allele frequency impact variant categorization for genetic screening of nonsyndromic hearing loss (NSHL) and other genetic…”
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Global Research on Hereditary Hearing Impairment Over the Last 40 Years: A Bibliometric Study by Tekin, Ahmet M, Bahşi, İlhan, Bayazit, Yıldırım A, Topsakal, Vedat

“…Research on hereditary hearing impairment has had several boosts to identify deafness-causing genes. The number of studies regarding the diagnosis and…”
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Combined retrosigmoid retrolabyrinthine vestibular nerve section: results of our experience over 10 years by Goksu, Nebil, Yilmaz, Metin, Bayramoglu, Ismet, Bayazit, Yildirim A

“…We aimed to evaluate the results of our experience in vestibular nerve sectioning (VN), which was performed using combined retrosigmoid-retrolabyrinthine…”
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Association of GJB2 gene mutation with cochlear implant performance in genetic non-syndromic hearing loss by Karamert, Recep, Bayazit, Yildirim A, Altinyay, Senay, Yılmaz, Akın, Menevse, Adnan, Gokdogan, Ozan, Gokdogan, Cagil, Ant, Ayca

“…Abstract Objective To analyze the association of GJB2 gene mutations with cochlear implant performance in children. Methods Sixty-five consecutive children who…”
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Cutaneous Involvement in Hodgkin's Lymphoma: Report of Two Cases by Erkiliç, Suna, Erbagci, Zulal, Koçer, N Emrah, Bayazit, Yildirim A, Camci, Celalettin

“…Hodgkin's lymphoma (HL) comprises 20 to 30% of all lymphomas. Skin involvement is almost always secondary to visceral or nodal involvement. Secondary cutaneous…”
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Primary leiomyoma of the thyroid gland by Erkiliç, Suna, Erkiliç, Ahmet, Bayazit, Yildirim A

“…Primary thyroid leiomyomas are rare, and only four cases have been reported to date. This is a report of an additional case of primary thyroid leiomyoma in a…”
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An overview of hereditary hearing loss by Bayazit, Yildirim A, Yilmaz, Metin

“…Understanding the genetic basis of hearing loss is important because almost 50% of profound hearing loss are caused by genetic factors and more than 120…”
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Significance of the catechol-O-methyltransferase gene polymorphism in migraine by Emin Erdal, M., Herken, Hasan, Yilmaz, Mustafa, Bayazit, Yildirim A.

“…The objective was to assess the significance of the catechol-o-methyltransferase (COMT) enzyme polymorphism in migraine. For this reason, 62 migraineurs and 64…”
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Labyrinthotomy or vestibulotomy in anatomic and congenital variations of the oval window and facial nerve by Al-Mazrou, Khalid A, Bayazit, Yildirim A

“…To present the results of our experience with labyrinthotomy or vestibulotomy in cases where the oval window is blocked by the facial nerve and in the presence…”
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Complications of pediatric auditory brain stem implantation via retrosigmoid approach by Bayazit, Yildirim A, Abaday, Ayça, Dogulu, Fikret, Göksu, Nebil

“…We aimed to present the complications of auditory brain stem implantations (ABI) in pediatric patients which were performed via retrosigmoid approach. Between…”
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Genetic Non-Syndromic Hearing Loss in Turkey by Bayazit, Yildirim A

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Langerhans cell related inflammatory reaction in laryngeal squamous cell carcinoma by Karakök, Metin, Bayazıt, Yıldırım A, Ucak, Ramazan, Özer, Enver, Kanlıkama, Muzaffer, Mumbuc, Semih, Sarı, İbrahim

“…The major cells involved in cancer cell kill are the T lymphocytes. However, T cells need to be activated upon antigen presentation, which is mediated by the…”
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Bone cement ossiculoplasty: incus to stapes versus malleus to stapes cement bridge by Bayazit, Yildirim A, Ozer, Enver, Kanlikama, Muzaffer, Durmaz, Tuba, Yilmaz, Metin

“…In this study, our purpose was to evaluate results of our experience with bone cement repair of ossicular discontinuity between the incus and stapes and…”
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Role of nitric oxide synthase gene intron 4 and exon 7 polymorphisms in obstructive sleep apnea syndrome by Bayazit, Yildirim A., Yilmaz, Metin, Erdal, Emin, Ciftci, Tansu Ulukavak, Ceylan, Alper, Kokturk, Oguz, Celenk, Fatih, Kemaloglu, Yusuf K.

“…The objective of our study was to assess the association of eNOS4 and eNOS296 polymorphisms of endothelial nitric oxide synthase (eNOS) gene with obstructive…”
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Bacterial Colonization in the External Ear Canal and Ear Tampon with Special Interest to Tympanoplasty by Bayazit, Nurhayat, Cevizci, Rasit, Bayazit, Yildirim A

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Hearing Amplification and Quality of Life with Bone Anchored Hearing Aid (BAHA) in Turkish Population by Gunduz, Bulent, Bilgin, Cumhur, Gokdogan, Cagil, Tutar, Hakan, Bayazit, Yildirim A, Goksu, Nebil

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Fully implantable hearing device in isolated congenital external ear canal atresia by Tutar, Hakan

“…Aural atresia is the congenital malformation of the ear characterized by partial or complete atresia of the external ear. Our aim is to show the effectiveness…”
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Association of Serotonin Transporter Gene Polymorphism with Obstructive Sleep Apnea Syndrome by Ylmaz, Metin, Bayazit, Yildirim A., Ciftci, Tansu Ulukavak, Erdal, M Emin, Urhan, Meral, Kokturk, Oguz, Kemaloglu, Yusuf K., Inal, Erdogan

“…Background and Objective: Obstructive sleep apnea syndrome (OSAS) is a common condition characterized by repetitive pharyngeal collapse during sleep and…”
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