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Pediatric Neurology|January 19, 2016
Correlation Between White Matter Lesions and Intelligence Quotient in Patients With Congenital Cytomegalovirus InfectionYuji Inaba, Mitsuo Motobayashi, Makoto Nishioka, et al.
Acta Oto-Laryngologica|April 28, 2022
Etiology of hearing loss affects auditory skill development and vocabulary development in pediatric cochlear implantation casesShin-Ya Nishio, Hideaki Moteki, Maiko Miyagawa, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutationHideaki Moteki, Hela Azaiez, Kevin T Booth, et al.
Scientific Reports|April 29, 2020
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing lossHiroki Miyajima, Hideaki Moteki, Timothy Day, et al.
Genes|September 19, 2019
Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of <i>OTOA</i>-Associated Hearing LossKenjiro Sugiyama, Hideaki Moteki, Shin-Ichiro Kitajiri, et al.
The Annals of Otology, Rhinology, and Laryngology|July 30, 2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic HybridizationHideaki Moteki, Hela Azaiez, Christina M Sloan-Heggen, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing lossNaoko Sakuma, Hideaki Moteki, Hela Azaiez, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 16, 2021
Identification of a Novel Copy Number Variation of EYA4 Causing Autosomal Dominant Non-syndromic Hearing LossTakashi Ishino, Yui Ogawa, Toru Sonoyama, et al.
Scientific Reports|February 29, 2020
Prevalence and clinical features of hearing loss caused by EYA4 variantsJun Shinagawa, Hideaki Moteki, Shin-Ya Nishio, et al.
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