Results 81 to 90 of about 1,850 (127)

A Systematic Review on the Role of the Stria Vascularis in Menière's Disease Pathogenesis. [PDF]

J Assoc Res Otolaryngol
Cruz-Granados P, Das S, Bagheri-Loftabad K, Lopez-Escamez JA.   +3 more
europepmc   +1 more source

Astrocytes connect specific brain regions through plastic networks. [PDF]

Nature
Cooper ML, Selles MC, Cammer M, Redd C, Gildea HK, Sall J, Chiurri KE, Cheung P, Wheeler DG, Saab AS, Liddelow SA, Chao MV.   +11 more
europepmc   +1 more source

Erratum: Investigation of the GJB6 Deletion Mutations Del (GJB6-D13s1830) and Del (GJB6-D13s1854) in Iranian Patients with Autosomal-Recessive Non-Syndromic Hearing Loss (ARNSHL)

Brazilian Archives of Biology and Technology, 2016
doaj   +1 more source

Utilization of genetics services in the diagnosis of hearing loss in newborns in the state of Ohio. [PDF]

J Community Genet
Barnett CL, Malhotra P, VanHorn A, Zaharieva B, Myers J, Riggs WJ, Jordan E.   +6 more
europepmc   +1 more source

A Novel 1259 bp Intragenic Deletion in the <i>GJB2</i> Gene in a Mexican Family with Congenital Profound Hearing Loss. [PDF]

Audiol Res
Oaxaca-Castillo D, Taño-Portuondo L, Rodríguez-Ballesteros M, Pérez-Mendoza G, García-González I, Canto-Herrera J, Domínguez-Ruiz M, Pinto-Escalante D, Vargas-Sierra O, Estrella-Castillo D, López-González P, Sosa-Escalante JE, Del Castillo I, González-Herrera L.   +13 more
europepmc   +1 more source

A novel deletion upstream of <i>POU3F4</i> in a Chinese family with X-linked deafness 2 and a literature review. [PDF]

Front Genet
Yang Y, Huang S, Liu Y, Mu D, Bai T, Jing X, Xing L, Liu H.   +7 more
europepmc   +1 more source

Etiologies of Early-Onset Hearing Impairment in Rwanda. [PDF]

Genes (Basel)
Uwibambe E, Mutesa L, Muhizi C, Ncogoza I, Twumasi Aboagye E, Dukuze N, Adadey SM, DeKock C, Wonkam A.   +8 more
europepmc   +1 more source

Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience. [PDF]

Orphanet J Rare Dis
Yi S, Yang Q, Wang L, Zhou X, Zhang S, Qian J, Yi S, Huang J, Chen J, Zhang Q, Chen F, Li J, Wei S, Zhang X, Zhang Q, Pan P, Qin Z, Luo J.   +17 more
europepmc   +1 more source

Exploring Embryonic and Postnatal Gene Therapy Approaches for GJB2-Related Deafness: A Scoping Review. [PDF]

Audiol Res
Caragli V, Martini A.
europepmc   +1 more source

Erratum: GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana

Frontiers in Genetics, 2019
Frontiers Production Office
doaj   +1 more source