Results 21 to 30 of about 179,655 (257)

Newborn hearing-screening project using transient evoked otoacoustic emissions: western sicily experience [PDF]

, 2006
OBJECTIVE: To study the incidence of congenital sensorineural hearing loss in all newborns introducing a screen test with a protocol no expensive, with a good "screen sensitivity" that could let an earlier identification of hearing impairment ...
FERRARA, M, MARTINES, Enrico, MARTINES, Francesco, MARTINES, M, PORRELLO, M   +4 more
core   +1 more source

Asymmetrically severe internal auditory canal hypoplasia: A case report. [PDF]

, 2020
We present a case of an otherwise healthy 20-month-old with congenital sensorineural hearing loss. CT and MR imaging demonstrated bilateral asymmetrically severe hypoplasia of the internal auditory canals and vestibulocochlear nerves.
Djalilian, Hamid R, Floriolli, David, Hasso, Anton, Martin, Jeremy W, Senturk, Cagin, Thompson, Matthew, Wishka, Christian   +6 more
core   +1 more source

Fluctuating Sensorineural Hearing Loss [PDF]

Audiology and Neurotology, 2019
<b><i>Background:</i></b> Several otologic conditions can present with fluctuating sensorineural hearing loss, including Ménière’s disease, autoimmune inner ear disease, and enlarged vestibular aqueduct. Although these 3 etiologies vary greatly, distinguishing between these conditions at initial presentation can be challenging ...
Hui Liu, Kunpeng Zhou, Xuemei Zhang, Kevin A. Peng   +3 more
openaire   +3 more sources

Noise-Induced Hearing Loss

Journal of Clinical Medicine, 2023
Noise-induced hearing loss (NIHL) is the second most common cause of sensorineural hearing loss, after age-related hearing loss, and affects approximately 5% of the world’s population.
Nirvikalpa Natarajan, Shelley A. Batts, K. Stankovic   +2 more
semanticscholar   +1 more source

Hearing impairment in Stickler syndrome: a systematic review [PDF]

, 2012
BACKGROUND: Stickler syndrome is a connective tissue disorder characterized by ocular, skeletal, orofacial and auditory defects. It is caused by mutations in different collagen genes, namely COL2A1, COL11A1 and COL11A2 (autosomal dominant inheritance ...
Acke, Frederic, De Leenheer, Els, Dhooge, Ingeborg, Malfait, Fransiska   +3 more
core   +2 more sources

Effects of cochlear implantation on binaural hearing in adults with unilateral hearing loss [PDF]

, 2018
A FDA clinical trial was carried out to evaluate the potential benefit of cochlear implant (CI) use for adults with unilateral moderate-to-profound sensorineural hearing loss.
Brown, Kevin D, Buchman, Craig A, Buss, Emily, Deres, Ellen J, Dillon, Margaret T, King, English R, Pillsbury, Harold C, Rooth, Meredith A   +7 more
core   +2 more sources

Sensorineural hearing loss and prematurity [PDF]

Archives of Disease in Childhood - Fetal and Neonatal Edition, 2000
To elucidate clinical antecedents of sensorineural hearing loss (SNHL) in very preterm infants.Case-control study.Fifteen children < 33 weeks' gestation with significant SNHL born between 1 January 1990 and 31 December 1994, detected within 9 months of birth, and 30 matched control children.Perinatal variables in the two groups were compared using non ...
Linda P. Hunt, Neil Marlow, Elaine S Marlow   +2 more
openaire   +3 more sources

Role of Oxidative Stress in Sensorineural Hearing Loss

International Journal of Molecular Sciences
Hearing is essential for communication, and its loss can cause a serious disruption to one’s social life. Hearing loss is also recognized as a major risk factor for dementia; therefore, addressing hearing loss is a pressing global issue.
M. Teraoka, Naohito Hato, Haruhiko Inufusa, Fukka You   +3 more
semanticscholar   +1 more source

Audio-vestibular symptoms in systemic autoimmune diseases [PDF]

, 2018
Immune-mediated inner ear disease can be primary, when the autoimmune response is against the inner ear, or secondary. The latter is characterized by the involvement of the ear in the presence of systemic autoimmune conditions. Sensorineural hearing loss
Adelchi, Croce, D'AGUANNO, VITTORIO, DE VINCENTIIS, Marco, DE VIRGILIO, ARMANDO, DI STADIO, Arianna, GRECO, Antonio, LONGO, Lucia, RALLI, MASSIMO   +7 more
core   +1 more source

Targeted Next Generation Sequencing Revealed a Novel Homozygous Loss-of-Function Mutation in ILDR1 Gene Causes Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in a Chinese Family

Frontiers in Genetics, 2019
Hereditary hearing impairment is one of the major and common birth defects in Chinese population. Non-syndromic sensorineural hearing loss (NSHL) is the most common types of hereditary hearing impairment.
J-X An, Jie-Wen Yang, Yan Wang, Yanxia Wang, Baicheng Xu, Guangmei Xie, Sanming Chai, Xiaoling Liu, Sijuan Xu, Xiaoxiao Wen, Qing He, Huijun Liu, Chen Li, S. Dey, Y. Ni, S. Banerjee   +15 more
semanticscholar   +1 more source