Results 161 to 170 of about 17,520 (209)

Cochlear Implant Challenges in Children with Ichthyosis: A Systematic Review. [PDF]

Genes (Basel)
Caragli V, Luppi L, Tegmeyer NC, Genovese E, Soloperto D.   +4 more
europepmc   +1 more source

A deafness-blindness syndrome results from ATF6-based disruption of the unfolded protein response. [PDF]

J Clin Invest
Joshi Y, Savas JN.
europepmc   +1 more source

Neonatal and Syndromic Forms of Diabetes. [PDF]

Curr Diab Rep
Gobble MRS, Stone SI.
europepmc   +1 more source

Hearing Loss in Connective Tissue Diseases: A Systematic Review. [PDF]

Eur J Rheumatol
Skare TL, Freire de Carvalho J.
europepmc   +1 more source

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

Herpes simplex virus 2-induced aseptic meningitis presenting with sudden deafness: A case report.

World J Clin Cases
Liu YC, Hsiao SH, Chen PR.
europepmc   +1 more source

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
europepmc   +1 more source

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
europepmc   +1 more source

The genetic susceptibility of SOD2 gene polymorphism in sudden sensorineural hearing loss (SSNHL). [PDF]

Glob Med Genet
Deng J, Ma G, Cao X, Chen Y, Hu L, Zhang J.   +5 more
europepmc   +1 more source

Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct. [PDF]

Mol Med
Bernardinelli E, Liuni R, Jamontas R, Tesolin P, Morgan A, Girotto G, Roesch S, Dossena S.   +7 more
europepmc   +1 more source