Effects of cochlear implantation on auditory temporal processing in single-sided deafness: a report of two cases von Gumus, Birgul, Incesulu, Armagan, Kaya, Ercan

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Effects of Oxygen Therapies in Experimental Acute Acoustic Trauma von Ata, Nazim, Kahraman, Erkan, Incesulu, Armagan, Yildirim, Engin

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International Otology Outcome Group and the International Consensus on the Categorization of Tympanomastoid Surgery von Yung, Matthew, James, Adrian, Merkus, Paul, Philips, John, Black, Bruce, Tono, Tetsuya, Linder, Thomas, Dornhoffer, John, İncesulu, Armagan

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Audio-vestibular and radiological analysis in Meniere’s disease von Kirbac, Arzu, Incesulu, Saziye Armagan, Toprak, Ugur, Caklı, Hamdı, Ozen, Hulya, Saylisoy, Suzan

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Investigation of the Presence of Biofilms in Chronic Suppurative Otitis Media, Nonsuppurative Otitis Media, and Chronic Otitis Media with Cholesteatoma by Scanning Electron Microsc... von Acar, Mustafa, Gurbuz, Melek Kezban, Incesulu, Armagan, Dag, Ilknur, Kaya, Ercan, Birdane, Leman

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Cochlear Implantation in Patients with Keratitis-Ichthyosis-Deafness Syndrome: A Report of Two Cases von Gumus, Birgul, Pinarbasli, Mehmet Ozgur, Incesulu, Armagan

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Analysis of cochlear implant revision surgeries von Gumus, Birgul, İncesulu, Armagan S., Kaya, Ercan, Kezban Gurbuz, M., Ozgur Pınarbaslı, M.

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The Importance of Thrombotic Risk Factors in the Development of Idiopathic Sudden Hearing Loss von Yildiz, Zuleyha, Ulu, Arzu, Incesulu, Armagan, Ozkaptan, Yalcin, Akar, Nejat

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Recurrent and private MYO15A mutations are associated with deafness in the Turkish population von Cengiz, F Basak, Duman, Duygu, Sirmaci, Asli, Tokgöz-Yilmaz, Suna, Erbek, Seyra, Oztürkmen-Akay, Hatice, Incesulu, Armagan, Edwards, Yvonne J K, Ozdag, Hilal, Liu, Xue Z, Tekin, Mustafa

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EAONO/JOS Joint Consensus Statements on the Definitions, Classification and Staging of Middle Ear Cholesteatoma von Yung, Matthew, Tono, Tetsuya, Olszewska, Ewa, Yamamoto, Yutaka, Sudhoff, Holger, Sakagami, Masafumi, Mulder, Jef, Kojima, Hiromi, İncesulu, Armağan, Trabalzini, Franco, Özgirgin, Nuri

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Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort von Bademci, Guney, Foster, Joseph, Mahdieh, Nejat, Bonyadi, Mortaza, Duman, Duygu, Cengiz, F.Basak, Menendez, Ibis, Diaz-Horta, Oscar, Shirkavand, Atefeh, Zeinali, Sirous, Subasioglu, Asli, Tokgoz-Yilmaz, Suna, Huesca-Hernandez, Fabiola, de la Luz Arenas-Sordo, Maria, Dominguez-Aburto, Juan, Hernandez-Zamora, Edgar, Montenegro, Paola, Paredes, Rosario, Moreta, Germania, Vinueza, Rodrigo, Villegas, Franklin, Mendoza-Benitez, Santiago, Guo, Shengru, Bozan, Nazim, Tos, Tulay, Incesulu, Armagan, Sennaroglu, Gonca, Blanton, Susan H., Ozturkmen-Akay, Hatice, Yildirim-Baylan, Muzeyyen, Tekin, Mustafa

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Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development von Bademci, Guney, Abad, Clemer, Cengiz, Filiz B, Seyhan, Serhat, Incesulu, Armagan, Guo, Shengru, Fitoz, Suat, Atli, Emine Ikbal, Gosstola, Nicholas C, Demir, Selma, Colbert, Brett M, Seyhan, Gozde Cosar, Sineni, Claire J, Duman, Duygu, Gurkan, Hakan, Morton, Cynthia C, Dykxhoorn, Derek M, Walz, Katherina, Tekin, Mustafa

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FOXF2 is required for cochlear development in humans and mice von Bademci, Guney, Abad, Clemer, Incesulu, Armagan, Elian, Fahed, Reyahi, Azadeh, Diaz-Horta, Oscar, Cengiz, Filiz B, Sineni, Claire J, Seyhan, Serhat, Atli, Emine Ikbal, Basmak, Hikmet, Demir, Selma, Nik, Ali Moussavi, Footz, Tim, Guo, Shengru, Duman, Duygu, Fitoz, Suat, Gurkan, Hakan, Blanton, Susan H, Walter, Michael A, Carlsson, Peter, Walz, Katherina, Tekin, Mustafa

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Anesthesia for a Child with Congenital Long QT Syndrome, a Case Report and Literature Review von Yaman, Ferda, Baydogan, Nurdan, Bilir, Ayten, Incesulu, Armagan

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The Effect of Nasal Obstruction after Different Nasal Surgeries Using Acoustic Rhinometry and Nasal Obstruction Symptom Evaluation Scale von Kahraman, Erkan, Cil, Yakup, Incesulu, Armagan

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The round window diameter in congenital aural atresia and comparison with sensorineural hearing loss and control group von Saylisoy, Suzan, Incesulu, Armagan, Kaya, Ercan, Pinarbasli, Ozgur, Adapinar, Baki

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Computed tomographic findings of X-linked deafness: a spectrum from child to mother, from young to old, from boy to girl, from mixed to sudden hearing loss von Saylisoy, Suzan, Incesulu, Armagan, Gurbuz, Melek Kezban, Adapinar, Baki

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A novel missense mutation in a C2 domain ofOTOF results in autosomal recessive auditory neuropathy von Tekin, Mustafa, Akcayoz, Duygu, Incesulu, Armagan

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Women in otolaryngology in Turkey: Insight of gender equality, career development and work-life balance von Eyigor Hülya Eyigör, Can, İlknur Haberal, İncesulu, Incesulu Armağan, Senol, Yeşim Şenol

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MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss von Bademci, Guney, Abad, Clemer, Incesulu, Armagan, Rad, Abolfazl, Alper, Ozgul, Kolb, Susanne M., Cengiz, Filiz B., Diaz-Horta, Oscar, Silan, Fatma, Mihci, Ercan, Ocak, Emre, Najafi, Maryam, Maroofian, Reza, Yilmaz, Elanur, Nur, Banu G., Duman, Duygu, Guo, Shengru, Sant, David W., Wang, Gaofeng, Monje, Paula V., Haaf, Thomas, Blanton, Susan H., Vona, Barbara, Walz, Katherina, Tekin, Mustafa

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