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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 27, 2010
Is preeclampsia a new risk factor for cochlear damage and hearing loss?Muzeyyen Yildirim Baylan, Umur Kuyumcuoglu, Ahmet Kale, et al.Indian Journal of Otolaryngology and Head and Neck Surgery : Official Publication of the Association of Otolaryngologists of India|March 2, 2013
An evaluation of preoperative computed tomography on patients with chronic otitis mediaMuzeyyen Yildirim-Baylan, Cihan Akgul Ozmen, Ramazan Gun, et al.International Journal of Pediatric Otorhinolaryngology|January 11, 2014
The pathology of silent otitis media: a predecessor to tympanogenic meningitis in infantsMuzeyyen Yildirim-Baylan, Patricia Schachern, Vladimir Tsuprun, et al.International Journal of Pediatric Otorhinolaryngology|April 22, 2014
Evidence for genotype-phenotype correlation for OTOF mutationsMuzeyyen Yildirim-Baylan, Guney Bademci, Duygu Duman, et al.Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|May 17, 2011
Association between type 1 diabetes mellitus and deposits in the semicircular canalsShigetoshi Yoda, Sebahattin Cureoglu, Muzeyyen Yildirim-Baylan, et al.The Journal of Craniofacial Surgery|May 30, 2013
Evaluation of hyperactivity, attention deficit, and impulsivity before and after adenoidectomy/adenotonsillectomy surgeryMuhammed Ayral, Muzeyyen Yildirim Baylan, Vefa Kinis, et al.Human Genetics|June 9, 2019
A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing lossClaire J Sineni, Muzeyyen Yildirim-Baylan, Shengru Guo, et al.Proceedings of the National Academy of Sciences of the United States of America|June 21, 2022
Mutations in <i>MINAR2</i> encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and miceGuney Bademci, María Lachgar-Ruiz, Mangesh Deokar, et al.Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2015
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohortGuney Bademci, Joseph Foster, Nejat Mahdieh, et al.Pageof 1