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A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy.
Rodríguez-Ballesteros M, Reynoso R, Olarte M, Villamar M, Morera C, Santarelli R, Arslan E, Medá C, Curet C, Völter C, Sainz-Quevedo M, Castorina P, Ambrosetti U, Berrettini S, Frei K, Tedín S, Smith J, Cruz Tapia M, Cavallé L, Gelvez N, Primignani P, Gómez-Rosas E, Martín M, Moreno-Pelayo MA, Tamayo M, Moreno-Barral J, Moreno F, del Castillo I. Rodríguez-Ballesteros M, et al. Among authors: arslan e. Hum Mutat. 2008 Jun;29(6):823-31. doi: 10.1002/humu.20708. Hum Mutat. 2008. PMID: 18381613
Electrocochleography in auditory neuropathy.
Santarelli R, Arslan E. Santarelli R, et al. Among authors: arslan e. Hear Res. 2002 Aug;170(1-2):32-47. doi: 10.1016/s0378-5955(02)00450-1. Hear Res. 2002. PMID: 12208539
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian family.
Alemanno MS, Cama E, Santarelli R, Carella M, Zelante L, Toffolatti L, Palladino T, Melchionda S, Arslan E. Alemanno MS, et al. Among authors: arslan e. Int J Pediatr Otorhinolaryngol. 2009 Jan;73(1):127-31. doi: 10.1016/j.ijporl.2008.09.019. Epub 2008 Nov 5. Int J Pediatr Otorhinolaryngol. 2009. PMID: 18990456
Global problem of drug-induced hearing loss.
Arslan E, Orzan E, Santarelli R. Arslan E, et al. Ann N Y Acad Sci. 1999 Nov 28;884:1-14. doi: 10.1111/j.1749-6632.1999.tb00277.x. Ann N Y Acad Sci. 1999. PMID: 10842579 Review.
622 results