Results 71 to 80 of about 166,190 (339)

Head Position Comparison between Students with Normal Hearing and Students with Sensorineural Hearing Loss

International Archives of Otorhinolaryngology, 2013
Introduction Head sense position is coordinated by sensory activity of the vestibular system, located in the inner ear. Children with sensorineural hearing loss may show changes in the vestibular system as a result of injury to the inner ear, which can ...
Renato de Souza Melo, Polyanna Waleska Amorim da Silva, Robson Arruda Souza, Maria Cristina Falcão Raposo, Karla Mônica Ferraz   +4 more
doaj   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat, Marjolaine Champagne, Mathieu Bergeron, Philippe Dodin, Nadia Roumeliotis   +4 more
wiley   +1 more source

Rehabilitation with Cochlear Implant in Patient with Harboyan Syndrome

International Archives of Otorhinolaryngology, 2013
Background Harboyan syndrome, defined as congenital corneal dystrophy associated with progressive sensorineural hearing loss, was first described by Harboyan in 1971.
Lauren Medeiros Paniagua, Maria Elza Kazumi Yamaguti Dorfman, Luiz Lavinsky, Pricila Sleifer   +3 more
doaj   +1 more source

Nationwide epidemiological survey of idiopathic sudden sensorineural hearing loss in Japan

Acta Oto-Laryngologica, 2017
Objectives: Using a large-scale nationwide survey database, we investigated the epidemiological characteristics for idiopathic SSNHL in Japan. Methods: The subjects for this analysis were patients registered in a Japanese multicentre database between ...
Ryosuke Kitoh, S. Nishio, K. Ogawa, S. Kanzaki, N. Hato, M. Sone, S. Fukuda, A. Hara, T. Ikezono, Kotaro Ishikawa, S. Iwasaki, K. Kaga, S. Kakehata, A. Matsubara, T. Matsunaga, T. Murata, Y. Naito, T. Nakagawa, K. Nishizaki, Y. Noguchi, H. Sano, Hiroaki Sato, Mikio Suzuki, H. Shojaku, Haruo Takahashi, H. Takeda, T. Tono, H. Yamashita, T. Yamasoba, S. Usami   +29 more
semanticscholar   +1 more source

Statistical shape modeling of the human inner ear through micro‐computed tomography imaging

The Anatomical Record, EarlyView.
In this study, 54 cadaveric temporal bone specimens underwent high‐resolution micro‐CT imaging. Images were semi‐automatically segmented and converted to 3D surface mesh models for morphological measurement and analysis. Statistical shape models were created for the inner ear, cochlea, and vestibular system, as well as for sex‐ and side‐based subgroups.
Carmine Spedaliere, Alexandra Vaupotic, Jaehyun Hwang, Khalil Husein, Mustafa Hafidh, Kyle Rioux, S. Alireza Rohani, Sumit K. Agrawal, Hanif M. Ladak   +8 more
wiley   +1 more source

Endometrial Stromal Cell Senescence: A Non‐Negligible Factor in Recurrent Pregnancy Loss

iMetaMed, EarlyView.
As populations age, links between female reproductive aging and infertility are increasingly evident. Cellular senescence, characterized by near‐irreversible cell‐cycle arrest and accumulation of damage, can impair tissue function. In the endometrium, aberrant senescence of endometrial stromal cells (EnSCs) may compromise receptivity, hinder embryo ...
Shuang Wu, Cenlan Bu, Qinzheng Xu, Xi Cheng, Junrong Zhang, Jinling Chen, Yun‐Zhao Xu   +6 more
wiley   +1 more source

Steroids and idiopathic sudden sensorineural hearing loss in Songklanagarind Hospital

Journal of Health Science and Medical Research (JHSMR), 2002
Objective: To study the effect of steroids on idiopathic sudden sensorineural hearing loss Material and Methods: Idiopathic sudden sensorineural hearing loss (ISHL) cases from 1998-2001 were collected and reviewed for demographic data, especially the ...
W Khaimook
doaj  

Identification of a Novel Likely Pathogenic Variant of DIAPH3 Associated With New Phenotype of Sensorineural Hearing Loss. [PDF]

Mol Genet Genomic Med
In this Chinese family with hereditary deafness, we identified a novel DIAPH3 point variant (NM_001042517.2:c.1472A>G). This variant manifests as late‐onset progressive sensorineural hearing loss, with congruent pure‐tone audiometry (PTA) and auditory brainstem response (ABR) thresholds.
Zeng L, Zheng Q, Wu X, Chen G, Xie L, Qiu W, Ning F, Bai L, Zhang Q.   +8 more
europepmc   +2 more sources

Clinical progress note: Rubella

Journal of Hospital Medicine, EarlyView.
Abstract Rates of rubella infection and congenital rubella syndrome decreased significantly since the introduction of the rubella vaccine in 1969. Endemic rubella was declared eliminated in the United States in 2004, and since 2012, all rubella cases in the United States have been associated with infections acquired abroad.
Adam E. Gailani, Walter Dehority, Sophie E. Katz   +2 more
wiley   +1 more source

The Role of Autoimmunity in the Pathogenesis of Sudden Sensorineural Hearing Loss

Journal of Neural Transplantation and Plasticity, 2018
Sudden sensorineural hearing loss (SSHL) is a clinically common acute symptom in otolaryngology. Although the incidence of SSHL has increased around the world in recent years, the etiology of the disease is still unclear.
Guangfei Li, Dan You, Jiaoyao Ma, Wen Li, Huawei Li, Shan Sun   +5 more
semanticscholar   +1 more source