91
Starr A, Picton TW, Sininger Y, Hood LJ, Berlin CI. Auditory neuropathy.
Brain. 1996; (119):741-753.
Starr A. The neurology of auditory neuropathy. In: Sininger Y, Starr A
(editors). Auditory neuropathy: a new perspective on hearing disorders.
Canada: Singular; 2001. 37-50.
Starr A, Sininger Y, Pratt H. The varieties of auditory neuropathy. J Basic Clin
Physiol Pharmacol. 2000; 11(3):215-30.
Starr A, Picton TW, Kim R. Pathophysiology of auditory neuropathy. In:
Sininger Y, Starr A (editors). Auditory Neuropathy: a new Perspective on
Hearing Disorders. Canada: Singular; 2001: 67-82.
Starr A, Zeng FG, Michalewski HJ, Moser T. Perspectives on auditory
neuropathy: disorders of inner hair cell, auditory nerve and their synapse. In:
Basbaum AI, Kaneko A, Shepherd GM, Westheimer G, eds. The Senses: A
Comprehensive Reference. In: Dallos P, Oertel D, eds. Auditions. San Diego,
CA: Academic Press 2008; (3): 397-412.
Sutton G, Gravel J, Hood L, Lightfoot G, Mason S, Sirimanna T, Stevens J,
Wood S. Assessment and management of auditory neuropathy/Auditory dys-
synchronyem A recommended protocol version 1.1. NHS [ citado em 2008
setembro 27]. 2008. Disponível em:
http://hearing.screening.nhs.uk/cms.php?folder=84.
Trautwein PG, Sininger YS, Nelson R. Cochlear implantation of auditory
nuropathy.J. Am. Acad. Audiol. 2000; (11):309-15.
Varga R, Kelley PM, Keats BJ, Starr A, Leal SM, Cohn E, Kimberling WJ.
Non-syndromic recessive auditory neuropathy is the result of mutations in the
otoferlin (OTOF) gene. J Med genet [periódico online] 2003 [citado 2008 set.
20]; 40: 45-50. Disponível em: www.jmedgenet.com.
Walton J, Gibson WPR, Sanli H, Prelog K. Predicting Cochlear Implant
Outcomes in Children With Auditory Neuropathy. Otology & Neurotology
2008; 29:302-309.
Warr WB, Guinan JJ. Efferent innervation of the organ of Corti, two separate
systems. Brain Res. 1979; 173 (1):152-55.
Webster, DB. Neuroscience of communication 2ª ed. Singular. Sandiego .
london. 1999. 249.
Yasunaga S, Grati M, Cohen-Salmon M, El-Amraoui A, Mustapha M, Salem
N, El-Zir E, Loiselet J , Petit C. A mutation in OTOF, encoding otoferlin, a
FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness. Nat
Genet 1999; 21: 363-369.