Search Results - "inner ear"

Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms by Hui Zhang, Jian Gao, Hanjun Wang, Mengli Liu, Shuangshuang Lu, Hongen Xu, Wenxue Tang, Guoxi Zheng

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Diffusion Tensor Imaging of Human Cerebellar Pathways and their Interplay with Cerebral Macrostructure by Zafer eKeser, Khader M Hasan, Benson eMwangi, Arash eKamali, Fehime Eymen Ucisik-Keser, Roy F Riascos, Nuray eYozbatiran, Gerard E. Francisco, Ponnada eNarayana

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Single-cell RNA-sequencing of stria vascularis cells in the adult Slc26a4 -/- mouse by Jin-Young Koh, Corentin Affortit, Paul T. Ranum, Cody West, William D. Walls, Hidekane Yoshimura, Jian Q. Shao, Brian Mostaert, Richard J.H. Smith

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A young soldier with Susac syndrome: a case report by Sabeeh Ahmed, Taimoor A. Khan, Talha Liaqat, Umer Ijaz, Haroon Sarfaraz

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Effect of sound and Bone Conduction Ultrasound stimulation on Tinnitus Inhibition by Nasrin Gohari, Abdolreza Sheibanizadeh, Mohammadreza Keihani

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Pioglitazone Represents an Effective Therapeutic Target in Preventing Oxidative/Inflammatory Cochlear Damage Induced by Noise Exposure by Fabiola Paciello, Fabiola Paciello, Fabiola Paciello, Anna Rita Fetoni, Anna Rita Fetoni, Anna Rita Fetoni, Rolando Rolesi, Matthew B. Wright, Claudio Grassi, Claudio Grassi, Diana Troiani, Gaetano Paludetti, Gaetano Paludetti

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Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling by Cong Ma, Lv Liu, Fang-Na Wang, Hai-Shen Tian, Yan Luo, Rong Yu, Liang-Liang Fan, Ya-Li Li

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eHealth for Addressing Balance Disorders in the Elderly: Systematic Review by Gaspar, Andréa G Martins, Lapão, Luís Velez

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AAV-ie-mediated UCP2 overexpression accelerates inner hair cell loss during aging in vivo by Chunli Zhao, Zijing Yang, Zhongrui Chen, Wenqi Liang, Shusheng Gong, Zhengde Du

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Patient‐Led Research to Develop a Training Programme for Restoring Musical Joy in Cochlear Implant Recipients: A Reflexive Process Evaluation by Marjo J. M. Maas, Joke Veltman, Philip J. van derWees, Cilia Beijk, Wendy J. Huinck, Adinda Y. M. Groenhuis, Huib Versnel, Gertjan Schuiling, Alex E. Hoetink

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Trajectory of hearing loss in children with unilateral hearing loss by Elizabeth M. Fitzpatrick, Elizabeth M. Fitzpatrick, Flora Nassrallah, Isabelle Gaboury, JoAnne Whittingham, JoAnne Whittingham, Bénédicte Vos, Doug Coyle, Andrée Durieux-Smith, Andrée Durieux-Smith, Marie Pigeon, Janet Olds, Janet Olds

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Clinical evaluation of cochlear implantation in children younger than 12 months of age by Yang Yang, Min Chen, Jun Zheng, Jinsheng Hao, Bing Liu, Wei Liu, Bei Li, Jianbo Shao, Haihong Liu, Xin Ni, Jie Zhang

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Utilizing cell-free DNA to validate targeted disruption of MYO7A in rhesus macaque pre-implantation embryos by Junghyun Ryu, Fernanda C. Burch, Emily Mishler, Martha Neuringer, Jon D. Hennebold, Carol Hanna

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The effects of altered BMP4 signaling in first branchial-arch-derived murine embryonic orofacial tissues by Jue Xu, Meiling Chen, Yanan Yan, Qiaoxue Zhao, Meiying Shao, Zhen Huang

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Hearing aid effectiveness after aural rehabilitation - individual versus group (HEARING) trial: RCT design and baseline characteristics by Heagerty Patrick J, Liu Chuan-Fen, Souza Pamela E, Collins Margaret P, Amtmann Dagmar, Yueh Bevan

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The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells by Andrew Parker, Sally H. Cross, Ian J. Jackson, Rachel Hardisty-Hughes, Susan Morse, George Nicholson, Emma Coghill, Michael R. Bowl, Steve D. M. Brown

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The effectiveness of the use of superelastic nitinol stapedial prostheses in comparison with titanium ones in the surgical treatment of patients with otosclerosis by Khassan M.A. Diab, Nikolai A. Daikhes, Olga A. Pashchinina, Svetlana V. Kokhanyuk, Anastasiya V. Smirnova, Amina G. Zukhba

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Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study by Santos Sofía, Soto-Varela Andrés, Gonzalez-Oller Carlos, Moreno Antonia, Gazquez Irene, Saenz-Lopez Pablo, Lopez-Escamez José A, Aran Ismael, Perez-Garrigues Herminio, Ibañez Águeda, Lopez-Nevot Miguel A

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Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects by Renata Watanabe Nonose, Karina Lezirovitz, Maria Teresa Balester de Mello Auricchio, Ana Carla Batissoco, Guilherme Lopes Yamamoto, Regina Célia Mingroni-Netto

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WFS1 autosomal dominant variants linked with hearing loss: update on structural analysis and cochlear implant outcome by Hui Dong Lim, So Min Lee, Ye Jin Yun, Dae Hee Lee, Jun Ho Lee, Seung-Ha Oh, Sang-Yeon Lee

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