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Clinical update on sensorineural hearing loss in Turner syndrome and the X‐chromosome
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2019Hearing loss is one of the major medical concerns in girls and women with Turner syndrome (TS) and has a negative effect on well‐being and quality of everyday life.
Åsa Bonnard +2 more
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Sensorineural hearing loss and mumps
British Journal of Audiology, 1987Out of 360 children with hearing loss seen during 1 year in the Haringey Audiology Unit, 21 had unilateral, sensorineural hearing loss. Sixteen had previously been checked to have no loss. It is strongly suspected that the hearing loss resulted from mumps, and therefore the disability in such children could be prevented by introducing mumps vaccination
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Sudden Sensorineural Hearing Loss
Otolaryngologic Clinics of North America, 1983Sudden sensorineural hearing loss is a frightening experience for the patient. The patient's worse fears concern tumors or stroke. Although the physician is often frustrated by a symptom whose cause at times is not apparent, every effort should be made to identify the causes of sudden sensorineural hearing loss and possible predisposing causes of ...
William L. Meyerhoff, Robert G. Anderson
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Inflammatory cytokines and mononuclear cells in sudden sensorineural hearing loss
Journal of Laryngology and Otology, 2019Objective This study evaluated tumour necrosis factor-α, interleukins 10 and 12, and interferon-γ levels, peripheral blood mononuclear cells, and clusters of differentiation 17c and 86 expression in unilateral sudden sensorineural hearing loss.
S. Yoon +4 more
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Sensorineural Hearing Loss in Cholesteatoma
Otology & Neurotology, 2016To determine whether middle ear cholesteatoma is associated with, sensorineural hearing loss, and whether patient age, cholesteatoma growth pattern, or, air bone gap size contribute to inner ear impairment.Cross-sectional comparative.A tertiary hospital.The subjects were 115 patients with middle ear cholesteatoma in one ear, and normal video-otoscopy ...
Luciana Fick Silveira Netto +3 more
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Sudden sensorineural hearing loss
British Journal of Hospital Medicine, 2012This article highlights the importance of recognizing sudden onset sensorineural hearing loss and summarizes the key diagnostic and management points. There is much to learn about its pathogenesis, and more trials are needed to establish evidence-based management.
Benjamin Stew +2 more
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2015
Previously termed nerve deafness, sensorineural hearing loss (SNHL) is due to impairments in the function of the cochlea or auditory nerve. The majority of cases are due to acquired causes, but congenital cases have many implications for childhood development and merit detailed discussion. Sensorineural hearing loss may coexist with conductive loss,
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Previously termed nerve deafness, sensorineural hearing loss (SNHL) is due to impairments in the function of the cochlea or auditory nerve. The majority of cases are due to acquired causes, but congenital cases have many implications for childhood development and merit detailed discussion. Sensorineural hearing loss may coexist with conductive loss,
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SENSORINEURAL HEARING LOSS IN CHILDREN
Pediatric Clinics of North America, 1996Hearing loss in infants and children may be sensorineural, conductive, or mixed. Severity varies from mild to profound. Educational initiatives aimed at children, parents, and primary health care providers could help prevent needless permanent hearing impairment.
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Acupuncture for Sensorineural Hearing Loss
Archives of Otolaryngology - Head and Neck Surgery, 1975Forty children, aged 9 to 16 years, with severe and profound sensorineural hearing loss received acupuncture five times weekly for three out of four weeks for a period of six months. The children had weekly audiometric evaluations. There were no clinically important differences during and post acupuncture.
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Sensorineural hearing loss in children
International Journal of Pediatric Otorhinolaryngology, 1999Sensorineural hearing loss in children, either congenital or acquired, has an incidence of 2-4 per million. Molecular diagnosis of early childhood deafness became available for some types of syndromal and non-syndromal forms and will offer different treatment modalities in the future.
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