References
- Bonnet C., Dresp B. Investigations of sensory magnitude and perceptual processing with reaction times. Psychologica 2001; 28: 63–86
- Buss, E., Hall, J.W. 3rd, Grose, J.H., & Hatch, D.R. 1998. Perceptual consequences of peripheral hearing loss: do edge effects exist for abrupt cochlear lesions?. Hear Res, 125((1–2)), 98–108.
- Chocholle R. Variation des temps de réaction auditifs en fonction de l'intensité à diverses fréquences. Année Psycho 1940; 41: 65–124
- Dietrich V., Nieschalk M., Stoll W., Rajan R., Pantev C. Cortical reorganization in patients with high frequency cochlear hearing loss. Hear Res 2001; 158: 95–101
- Eggermont J.J., Komiya H. Moderate noise trauma in juvenile cats results in profound cortical topographic map changes in adulthood. Hear Res. 2000; 142(1–2)89–101
- Fowler F.P. A method for the early detection of otosclerosis. Arch Otolaryngol 1936; 24: 731–41
- Gabriel, D., Veuillet, E., Vesson, J.F. & Collet, L., At press. Secondary functional plasticity: Influence of rehabilitation on auditory privation plasticity.
- Gatehouse S., Gordon J. Response times to speech stimuli as measures of benefit from amplification. Br J Audiol 1990; 24: 63–8
- Gelfand S.A., Silman S., Ross L. Long-term effects of monaural, binaural, and no amplification in subjects with bilateral hearing loss. Scand Audiol 1987; 16: 201–7
- Hurley R.M. Onset of auditory deprivation. J Am Acad Audiol 1999; 10: 529–34
- Link S.W. The wave theory of difference and similarity. Erlbaum, Hillsdale, NJ 1992
- McDermott H.J., Lech M., Kornblum M.S., Irvine D.R. Loudness perception and frequency discrimination in subjects with steeply sloping hearing loss: Possible correlates of neural plasticity. J Acoust Soc Am 1998; 104: 2314–25
- Pfingst B.E., Hienz R., Kimm J., Miller J. Reaction-time procedure for measurement of hearing. I. Suprathreshold functions. J Acoust Soc Am 1975; 57: 421–30
- Pieron H. Recherche sur les lois de variation des temps de latence sensorielle en fonction des intensités excitatrices. Année Psycho 1914; 20: 17–96
- Pins D., Bonnet C. On the relation between stimulus intensity and processing time: Piéron's law and choice reaction time. Perception and psychophysics 1996; 58: 390–400
- Rajan R., Irvine D.R., Wise L.Z., Heil P. Effect of unilateral partial cochlear lesions in adult cats on the representation of lesioned and unlesioned cochleas in primary auditory cortex. J Comp Neurol 1993; 338: 17–49
- Robertson D., Irvine D.R. Plasticity of frequency organization in auditory cortex of guinea pigs with partial unilateral deafness. J Comp Neurol 1989; 282: 456–71
- Scharf B. Loudness. Handbook of perception, E.C. Carterette, M.P. Friedman. Academic Press, New York 1978; IV: 187–242
- Schwaber M.K., Garraghty P.E., Kaas J.H. Neuroplasticity of the adult primate auditory cortex following cochlear hearing loss. Am J Otol. 1993; 14(3)252–8
- Seitz P.F., Rakerd B. Auditory stimulus intensity and reaction time in listeners with longstanding sensorineural hearing loss. Ear Hear 1997; 18: 502–12
- Steinberg J.C., Gardner M.B. The dependency of hearing impairment on sound intensity. J Acoust Soc Am 1937; 9: 11–23
- Thai-Van H., Micheyl C., Norena A., Collet L. Local improvement in auditory frequency discrimination is associated with hearing-loss slope in subjects with cochlear damage. Brain 2002; 125: 524–37
- Thai-Van H., Micheyl C., Moore B.C., Collet L. Enhanced frequency discrimination near the hearing loss cut-off: A consequence of central auditory plasticity induced by cochlear damage?. Brain 2003; 126: 2235–45
- Willott J.F, Carlson S., Chen H. Prepulse inhibition of the startle response in mice: Relationship to hearing loss and auditory system plasticity. Behav Neurosci 1994; 108: 703–13