Ipoacusia in età infantile. Diagnosi e trattamento

2355

di Laura Siri, Maria Adelaide Zucchinali, Laura Cervetto, Paola Mori, Benedetta Cerruti

Centro di Riabilitazione La Nostra Famiglia, Varazze
Ambulatorio di Neuropsichiatria Infantile, SC di Neonatologia e Pediatria, Ospedale San Paolo, Savona

Il Pediatra 2016; 2: 52-56

 

Bibliografia

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  6. Gualandi E, Ravani A, Berto A, et al. Occurrence of del (GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele. Acta Otolaryngol Suppl 2004; 552: 29-34.
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  8. Suppiej A, Rizzardi E, Zanardo V, et al. Reliability of hearing screening in high-risk neonates: Comparative study of otoacoustic emission, automated and conventional auditory brainstem response. Clin Neurophysiol 2007; 118: 869-876.
  9. Warren FM, Wiggins RH, Pitt C, et al. Apparent cochlear nerve aplasia: to implant or not to implant? Pubblicazione ufficiale di otologia e neurotologia della American Otological Society American Neurotology Society e della European Academy of Otology and Neurotology 2010; 31(7): 1088-1094.
  10. Lee Y-M, Kim L-S, Jeong S-W, Kim J-S, Chung S-H. Performance of children with mental retardation after cochlear implantation: speech perception, speech intelligibility, and language development. Actaotolaryngologica 2010; 130(8): 924-934.
  11. Linee guida SIO 2009 Impianti Cocleari. Acta Otorhinolaryngoiatrica 2009; 3: 1-5.