Results 31 to 40 of about 28,155 (144)

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

open access: yes, 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   +3 more
core   +2 more sources

Post vaccinal temporary sensorineural hearing loss [PDF]

open access: yes, 2018
In our systematic research we identified four studies concerning the onset of neurological adverse events following vaccination and two excluding this association.
De Cesare, Donato Pompeo   +8 more
core   +1 more source

Non-Syndromic Sensorineural Prelingual and Postlingual Hearing Loss due to COL11A1 Gene Mutation [PDF]

open access: yes, 2021
This paper aims to present a third world case of Non-Syndromic sensorineural hearing loss (NSHL) due to a novel missense variant in COL11A1 gene, defined as DFNA37 non-syndromic hearing loss.
Andrea Ciorba   +6 more
core   +1 more source

Bilateral Sudden Sensorineural Hearing Loss after Treatment of Aneurysmal Subarachnoid Hemorrhage by Angiographic Embolization: A Case Report

open access: yesTurkish Archives of Otorhinolaryngology, 2014
Bilateral sudden sensorineural hearing loss is a rare otologic emergency and constitutes 0.44%-4.9% of overall sudden sensorineural hearing loss cases. Microvascular dysfunction secondary to systemic cardiovascular diseases, such as embolism, vasospasm ...
Çağatay Han Ülkü, Abitter Yücel
doaj   +1 more source

Characteristics of hearing-impairment among patients in Ghana [PDF]

open access: yes, 2008
The causes, and characteristics of hearing-impairment were determined prospectively among six thousand, four hundred and twenty-eight (6,428) patients who reported at the Komfo Anokye Teaching Hospital (KATH) with hearing problems.
Amedofu, GK, Antwi, BB, Ocansey, G
core   +2 more sources

Sensorineural hearing loss and prematurity [PDF]

open access: yesArchives 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   +2 more
openaire   +3 more sources

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

open access: yes, 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   +7 more
core   +2 more sources

Hearing Profile of Children Below Three Years Old at Jatinangor Integrative Health Care Center, West Java, Indonesia [PDF]

open access: yes, 2022
Background: Hearing function is one of the most important factors affecting children’s development process. The first three years of life is a golden period of growth and development of children.
Allisha, Fidkya   +2 more
core   +2 more sources

Analysis of congenital hearing loss after neonatal hearing screening

open access: yesFrontiers in Pediatrics, 2023
IntroductionNeonates undergo neonatal hearing screening to detect congenital hearing loss at an early stage. Once confirmed, it is necessary to perform an etiological workup to start appropriate treatment.
Gill Verstappen   +6 more
doaj   +1 more source

Hereditary sensorineural hearing loss in a bird [PDF]

open access: yesNaturwissenschaften, 1994
The avian cochlea is the principal model for the investigation of hair-cell regeneration and the recovery of function in the vertebrate auditory periphery [1]. This capacity for repair in birds would seem to preclude permanent sensorineural hearing loss involving hair cells, which is the most common cause of hearing disabilities in humans [2]. Here, we
Gleich, Otto   +2 more
openaire   +3 more sources

Home - About - Disclaimer - Privacy