Results 191 to 200 of about 139,917 (247)

An efficient strategy for establishing a model of sensorineural deafness in rats.

Neural Regen Res, 2015
Ma L, Yi HJ, Yuan FQ, Guo WW, Yang SM.
europepmc   +1 more source

Neonatal and Syndromic Forms of Diabetes. [PDF]

Curr Diab Rep
Gobble MRS, Stone SI.
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Hearing Loss in Connective Tissue Diseases: A Systematic Review. [PDF]

Eur J Rheumatol
Skare TL, Freire de Carvalho J.
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Whole exome sequencing diagnosing syndromic and non-syndromic hearing loss with expansion of the phenotypic spectrum related to TMC1 variants. [PDF]

Eur J Pediatr
Elbagoury NM, Ashaat EA, Mekkawy MK, Mohamed RY, Askoura AM, Milad PM, Essawi ML.   +6 more
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Speech, Spatial, and Qualities of Hearing Scale and Tinnitus Functional Index Improvements After Cochlear Implant Surgery for Single-Sided Deafness. [PDF]

Laryngoscope Investig Otolaryngol
Shapiro SB, Mowery TM, Wackym PA.
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Sensorineural hearing loss and CT abnormalities in otosclerosis: Insights from otopathological specimens. [PDF]

Braz J Otorhinolaryngol
Monsanto RDC, Malpaga CMD, Yamashita HK, Suzuki FB, Penido NO.   +4 more
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Genetic Sensorineural Deafness in Adults

Annals of Otology, Rhinology & Laryngology, 1975
Progressive genetic sensorineural hearing loss is a common problem in adults which is frequently incorrectly diagnosed or escapes diagnosis as to etiology altogether. If the hearing problem becomes manifest in the twilight of the patient's life it is often identified with the nondescriptive term “presbycusis.” In all patients with sensorineural ...
Rolf F. Ulvestad, David G. Hanson, Michael M. Paparella, K. N. Rao   +3 more
openaire   +3 more sources

Familial Progressive Sensorineural Deafness

Archives of Otolaryngology - Head and Neck Surgery, 1969
DEAFNESS resulting from genetic causes may be present at time of birth (congenital) or may develop subsequent to birth (acquired). In congenital deafness the end-or-gan of hearing may not develop in the first trimester (aplasia). It is also conceivable, but not proven, that a fully differentiated sense organ may degenerate during the second and third ...
Shigeru Sugiura, Michael M. Paparella, Tomoyuki Hoshino   +2 more
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Hereditary progressive sensorineural deafness

The Journal of Laryngology & Otology, 1976
Progressive 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, K. E. Hedberg, F. Suga, S. K. Maitland   +3 more
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Unilateral Sensorineural Deafness in Children

Otolaryngology–Head and Neck Surgery, 1988
Heredity, 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
openaire   +3 more sources