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Sensorineural hearing loss in neurobrucellosis
The Journal of Laryngology & Otology, 1993AbstractA case of neurobrucellosis presenting to the otologist with sensorineural hearing loss (SNHL) as the predominant clinical feature is reported. The diagnostic features and treatment options are discussed and the need for prolonged combination treatment to prevent relapse and further deterioration of hearing stressed. SNHL in neurobrucellosis has
Ratna Thomas +3 more
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Sensorineural Impairment in Unilateral Otosclerosis
Annals of Otology, Rhinology & Laryngology, 1975Audiometric findings were evaluated in a group of patients with clinical unilateral otosclerosis. A comparison was made between bone conduction threshold in the better hearing ear and the ear with the mixed hearing loss. Over 50% of the patients had a significant elevation in the bone conduction thresholds in the ear with clinical otosclerosis as ...
Fred H. Linthicum, A. S. Lalani
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HISTOPATHOLOGY OF PROFOUND SENSORINEURAL DEAFNESSa
Annals of the New York Academy of Sciences, 1983In all the cases of profound deafness that we examined, the sensory epithelium along the basilar membrane had severely degenerated. However, ganglion cell counts and peripheral fiber estimates demonstrated a high degree of variability when analyzed with respect to the state of the organ of Corti or the etiology of the original cochlear disorder.
Raäl Hinojosa, Mitchell Marion
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Unilateral Sensorineural Deafness in Children
Otolaryngology–Head and Neck Surgery, 1988Heredity, viral infection, and head or acoustic trauma are considered the common etiologies for a unilateral sensorineural deafness in children. The incidence of perilymphatic fistula in a unilateral hearing loss is still unknown. Inner ear‐related symptoms in children are scarce, and little diagnostic laboratory testing is available.
William H. Friedman, Izak H. Kielmovitch
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Database for sensorineural hearing loss
International Journal of Pediatric Otorhinolaryngology, 1996We are creating a bank of EBV immortalized lymphoblast cells and extracted DNA taken from the blood of deaf children and their relatives, in order to study the molecular basis of hereditary deafness. We have established a corresponding database for sensorineural hearing loss that records clinical data for each entered specimen.
Andrew J. Fishman, Nancy Sculerati
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Reversible sensorineural hearing loss
International Journal of Pediatric Otorhinolaryngology, 2002We present an unusual case of temporary sensorineural hearing loss in a 6-year-old child due to carbon monoxide. This was shown on both the audiograms and confirmed with objective testing using otoacoustic emissions. Carbon monoxide poisoning is one of the few recognised causes of reversible sensorineural hearing loss, though it may also lead to a ...
C Lee, P Robinson, J Chelladurai
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Journal of Paediatrics and Child Health, 1991
ABSTRACTHearing losses in children are disabling and frequently unrecognized. Children with persistent uncorrected hearing impairment are at high risk for speech and language delays, behavioural problems, and socialization and learning difficulties. Although most hearing impairment in childhood is conductive in type. about 1 in 1000 Australian children
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ABSTRACTHearing losses in children are disabling and frequently unrecognized. Children with persistent uncorrected hearing impairment are at high risk for speech and language delays, behavioural problems, and socialization and learning difficulties. Although most hearing impairment in childhood is conductive in type. about 1 in 1000 Australian children
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Hereditary progressive sensorineural deafness
The Journal of Laryngology & Otology, 1976Progressive sensorineural hearing losses found in seven members of three families are presented. Genetic transmission patterns in the study appeared to be autosomal dominant in two families and recessive in one family. The common audiological features of these cases include bilaterally symmetrical audiometric configuration and fairly good speech ...
R. F. Naunton +3 more
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[Hereditary sensorineural deafness].
La Revue du praticien, 2000Deafness is the most common sensory defect. The investigation of the cause of deafness is critical for genetic counselling, and sometimes for appropriate management of associated pathologies. About two thirds of cases of congenital deafness are genetic forms, and the proportion is probably similar concerning the forms of deafness that appears during ...
Denoyelle, Françoise +3 more
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Epidemiology of Sensorineural Hearing Loss
International Journal of Audiology, 1973The paper is based on the author's epidemiological studies of sensorineural hearing loss in Ghana, Jamaica, Nigeria and the United Kingdom. Basically, the method has been one of direct examination of random or total samples. Such a study is more difficult than a study of conductive hearing loss because there is no qualitative difference between ...
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