References
- Bertorini T., Narayanaswami P., Rashed H. 2004. Charcot-Marie-Tooth disease (hereditary motor sensory neuropathies) and hereditary sensory and autonomic neuropathies. The Neurologist, 10: 327–337.
- Charcot J.M., Marie P. 1886. Sur une forme particuliere d'atrophie musculaire progressive, souvent familial debtant par les pieds et les jambs et atteignant plus tard les mains. Revue medicale, Paris, 6: 97–138.
- Gibson W.P.R., Graham J.M. 2008. Editorial: ‘Auditory neuropathy’ and cochlear implantation – myths and facts. Cochlear Implants International, 9(1): 1–7.
- Jani-Acsadi A., Krajewski K., Shy M.E. 2008. Charcot-Marie-Tooth neuropathies: diagnosis and management. Seminars in Neurology, 28(2): 185–194.
- Joo I.S., Ki C.S., Joo S.Y., Huh K., Kim J.W. 2004. A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness. Neuromuscular Disorders, 14(5): 325–328.
- Kovach M.J., Campbell K.C., Herman K., Waggoner B., Gelber D., Hughes L.F., et al. 2002. Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: delineation of the clinical features and review of the literature. American Journal of Medical Genetics, 108(4): 295–303.
- Krajewski K.M., Lewis R.A., Fuerst D.R. 2000. Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A. Brain, 123(7): 1516–1517.
- Mason J.C., Michele A.D., Stevens C., Ruth R.A., Hashisaki G.T. 2003. Cochlear implantation in patients with auditory neuropathy of varied etiologies. The Laryngoscope, 113: 45–49.
- Postelmans J.T.F., Stokroos R.J. 2006. Cochlear implantation in a patient with deafness induced by Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathies). Journal of Laryngology & Otology, 120: 508–510.
- Raglan E., Prasher D.K., Trinder E., Rudge P. 1987. Auditory function in hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Acta Oto-Laryngologica (Stockholm), 103: 50–55.
- Rapin I., Gravel J. 2003. ‘Auditory neuropathy’: physiologic and pathologic evidence calls for more diagnostic specificity. International Journal of Pediatric Otorhinolaryngology, 67: 707–728.
- Runge-Samuelson C.L., Drake S., Wackym P.A. 2008. Quantitative analysis of electrically evoked auditory brainstem responses in implanted children with auditory neuropathy/dyssynchrony. Otology & Neurotology, 29: 174–178.
- Sambuughin N., de Bantel A., McWilliams S., Sivakumar K. 2003. Deafness and CMT disease associated with a novel four amino acid deletion in the PMP22 gene. Neurology, 60: 506–508.
- Shallop J.K., Peterson M.A., Facer G.W., Fabry L.B., Driscoll C.L.W. 2001. Cochlear implants in five cases of auditory neuropathy: postoperative findings and progress. The Laryngoscope, 111: 555–562.
- Sininger Y.S., Trautwein P. 2002. Electrical stimulation of the auditory nerve via cochlear implants in patients with auditory neuropathy. Annals of Otology, Rhinology & Laryngol Supplement, 189: 29–31.
- Starr A., Picton T.W., Sininger Y., Hood L.J., Berlin C.I. 1996. Auditory neuropathy. Brain, 119: 741–753.
- Szigeti K., Lupski J.R. 2009. Charcot-Marie–Tooth disease. European Journal of Human Genetics, 17: 703–710.
- Tooth H.H. 1886. The peroneal type of progressive muscular atrophy. Dissertation, St Bartholomew's, London.
- Zeng F.G., Oba S., Garde S., Sininger Y., Starr A. 1999. Temporal and speech processing deficits in auditory neuropathy. NeuroReport, 10: 3429–3435.