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Universal newborn hearing screening in the Italian Region of Sicily in 2018.
Ferlito S, Maniaci A, Cocuzza S, La Mantia I, Di Mauro P, Poli G, Maiolino L, Coco S, Merlino F, Maltese M, Ragliani M, Russo M, Gulino A, Azieli C, Martines F, Galletti F, Bubbico L. Ferlito S, et al. Acta Otorhinolaryngol Ital. 2021 Aug;41(4):356-363. doi: 10.14639/0392-100X-N1162. Acta Otorhinolaryngol Ital. 2021. PMID: 34533539 Free PMC article.
Therefore, the main objective was to collect in the year 2018 the following data: number of newborns screened for hearing loss, number of infants "referred" to transiently evoked otoacoustic emissions (TEOAE), number of infants with pathologic auditory brainstem res …
Therefore, the main objective was to collect in the year 2018 the following data: number of newborns screened for hearing loss …
Insulin for the treatment of women with gestational diabetes.
Brown J, Grzeskowiak L, Williamson K, Downie MR, Crowther CA. Brown J, et al. Cochrane Database Syst Rev. 2017 Nov 5;11(11):CD012037. doi: 10.1002/14651858.CD012037.pub2. Cochrane Database Syst Rev. 2017. PMID: 29103210 Free PMC article. Review.
Low-quality evidence also found no clear differences between groups for rates of neurosensory disabilities in later childhood: hearing impairment (RR 0.31, 95% CI 0.01 to 7.49; one study, 93 children), visual impairment (RR 0.31, 95% CI 0.03 to 2.90; o …
Low-quality evidence also found no clear differences between groups for rates of neurosensory disabilities in later childhood: hea …
Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History.
Nisenbaum E, Yan D, Shearer AE, de Joya E, Thielhelm T, Russell N, Staecker H, Chen Z, Holt JR, Liu X. Nisenbaum E, et al. Audiol Neurootol. 2023;28(6):407-419. doi: 10.1159/000528766. Epub 2023 Jun 16. Audiol Neurootol. 2023. PMID: 37331337 Free PMC article. Review.
BACKGROUND: Mutations in TMPRSS3 are an important cause of autosomal recessive non-syndromic hearing loss. The hearing loss associated with mutations in TMPRSS3 is characterized by phenotypic heterogeneity, ranging from mild to profound heari …
BACKGROUND: Mutations in TMPRSS3 are an important cause of autosomal recessive non-syndromic hearing loss. The hearing …