Assessment of auditory plasticity using psychoacoustic and electrophysiological measurements

References

• Elbert T, Pantev C, Wienbruch C, Rockstroh B, Taub E. Increased cortical representation of the fingers of the left hand in string players. Science 1995; 270: 305–7
   PubMed Web of Science ®Google Scholar
• Pascual-Leone A, Torres F. Plasticity of the sensorimotor cortex representation of the reading finger in Braille readers. Brain 1993; 116: 39–52
   PubMed Web of Science ®Google Scholar
• Sterr A., Müller MM, Elbert T, Rockstroh B, Pantev C, Taub E. Changed perceptions in Braille readers. Nature 1998; 391: 134–5
   PubMed Web of Science ®Google Scholar
• Sterr A, Müller MM, Elbert T, Rockstroh B, Pantev C, Taub E. Perceptual correlates of changes in cortical representation of fingers in blind multifinger Braille readers. J Neurosci 1998; 18: 4417–23
   PubMed Web of Science ®Google Scholar
• Recanzone GH, Merzenich MM, Schreiner CE. Changes in the distributed temporal response properties of SI cortical neurons reflect improvements in performance on a temporally based tactile discrimination task. J Neurophysiol 1992; 67: 1071–91
   PubMed Web of Science ®Google Scholar
• Recanzone GH, Schreiner CE, Merzenich MM. Plasticity in the frequency representation of primary auditory cortex following discrimination training in adult owl monkeys. J Neurosci 1993; 13: 87–103
   PubMed Web of Science ®Google Scholar
• Ramachandran VS. Behavioural and magnetoencephalographic correlates of plasticity in the adult human brain. Proc Nat Acad Sci USA 1993; 90: 10413–20
   PubMed Web of Science ®Google Scholar
• Kaas JH. Plasticity of sensory and motor maps in adult mammals. Annu Rev Neurosci 1991; 14: 137–67
   PubMed Web of Science ®Google Scholar
• Kaas JH, Krubitzer LA, Chino YM, Langston AL, Polley EH, Blair N. Reorganization of retinotopic cortical maps in adult mammals after lesions of the retina. Science 1990; 248: 229–31
   PubMed Web of Science ®Google Scholar
• Gilbert CD, Wiesel TN. Receptive field dynamics in adult primary visual cortex. Nature 1992; 356: 150–2
   PubMed Web of Science ®Google Scholar
• Jones EG, Pons TP. Thalamic and brainstem contributions to large-scale plasticity of primate somatosensory cortex. Science 1998; 282: 1121–5
   PubMed Web of Science ®Google Scholar
• Rajan R, Irvine DR, Wise LZ, 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
   PubMed Web of Science ®Google Scholar
• Robertson D, Irvine DR. Plasticity of frequency organization in auditory cortex of guinea pigs with partial unilateral deafness. J Comp Neurol 1989; 282: 456–71
   PubMed Web of Science ®Google Scholar
• Schwaber MK, Garraghty PE, Kaas JH. Neuroplasticity of the adult primate auditory cortex following cochlear hearing loss. Am J Otol 1993; 14: 252–8
   PubMedGoogle Scholar
• Irvine DRF, Rajan R. Plasticity in the mature auditory system. Advances in Hearing Research, GA Manley, GM Klump, C Köppl, C Fastl, H Oeckinghaus. World Scientific, Singapore 1995; 3–23
   Google Scholar
• 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
   PubMed Web of Science ®Google Scholar
• McDermott HJ, Lech M, Kornblum MS, Irvine DR. 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
   PubMed Web of Science ®Google Scholar
• 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
   PubMed Web of Science ®Google Scholar
• Thai-Van H, Micheyl C, Moore BCJ, 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
   PubMed Web of Science ®Google Scholar
• Thai-Van H, Micheyl C, Norena A, Veuillet E, Gabriel D, Collet L. Enhanced frequency discrimination in hearing impaired individuals. A review of perceptual correlates of central neural plasticity induced by cochlear damage. Hear Res 2007; 233: 14–22
   PubMed Web of Science ®Google Scholar
• Gabriel D, Veuillet E, Vesson JF, Collet L. Rehabilitation plasticity: influence of hearing aid fitting on frequency discrimination performance near the hearing loss cut-off. Hear Res 2006; 213: 49–57
   PubMed Web of Science ®Google Scholar
• Gatehouse S. Apparent auditory deprivation effects of late onset: the role of presentation level. J Acoust Soc Am 1989; 86: 2103–6
   PubMed Web of Science ®Google Scholar
• Gelfand SA, 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
   PubMed Web of Science ®Google Scholar
• Silman S, Gelfand SA, Silverman C. Late-onset auditory deprivation: effects of monaural versus binaural HAs. J Acoust Soc Am 1984; 76: 1357–62
   PubMed Web of Science ®Google Scholar
• Silman S, Silverman C, Emmer MB, Gelfand SA. Adult-onset auditory deprivation. J Acoust Soc Am 1992; 3: 390–6
   Google Scholar
• Boothroyd A. Recovery of speech perception performance after prolonged auditory deprivation: case study. J Am Acad Audiol 1993; 4: 331–6
   PubMedGoogle Scholar
• Arlinger S, Gatehouse S, Bentler RA, Byrne D, Cox RM, Dirks DD, et al. Report of the Eriksholm Workshop on auditory deprivation and acclimatization. Ear Hear 1996; 17(Suppl 3)S87–98
   Web of Science ®Google Scholar
• Philibert B, Collet L, Vesson JF, Veuillet E. Intensity-related performances are modified by long-term hearing aid use: a functional plasticity?. Hear Res 2002; 165: 142–51
   PubMed Web of Science ®Google Scholar
• Philibert B, Collet L, Vesson JF, Veuillet E. The auditory acclimatization effect in sensorineural hearing-impaired listeners: evidence for functional plasticity. Hear Res 2005; 205: 131–42
   PubMed Web of Science ®Google Scholar
• Hugdahl K. Handbook of dichotic listening: theory, methods and research. John Wiley & Sons, New York 1988
   Google Scholar
• Galaburda A, LeMay M, Kemper T, Gerschwind N. Right-left asymmetries in the brain. Science 1978; 199: 852–6
   PubMed Web of Science ®Google Scholar
• Philibert B, Veuillet E, Collet L. Functional asymmetries of crossed and uncrossed medial olivocochlear efferent pathways in humans. Neurosci Lett 1998; 253: 99–102
   PubMed Web of Science ®Google Scholar
• Philibert B, Collet L, Vesson JF, Veuillet E. Auditory rehabilitation effects on speech lateralization in hearing-impaired listeners. Acta Otolaryngol 2003; 123: 172–5
   PubMed Web of Science ®Google Scholar
• Kimura D. Cerebral dominance and the perception of verbal stimuli. J Psychol 1961; 15: 166–71
   Web of Science ®Google Scholar
• Abramson A, Lisker L. Discriminability along the voicing continuum: cross- language tests. Proceedings of the Sixth International Congress of Phonetic Sciences. Academic Press, Prague 1967; 569–73
   Google Scholar
• Serniclaes W. Etude expérimentale de la perception du trait de voisement des occlusives du français. Thèse de doctorat en sciences psychologiques. Université Libre de Bruxelles, Belgium 1987
   Google Scholar
• Liégeois-Chauvel C, de Graaf JB, Laguitton V, Chauvel P. Specialization of left auditory cortex for speech perception in man depends on temporal coding. Cereb Cortex 1999; 9: 484–96
   PubMed Web of Science ®Google Scholar
• Trebuchon-Da Fonseca A, Giraud K, Badier JM, Chauvel P, Liegeois-Chauvel C. Hemispheric lateralization of voice onset time (VOT) comparison between depth and scalp EEG recordings. Neuroimage 2005; 27: 1–14
   PubMed Web of Science ®Google Scholar
• Laguitton V, de Graaf JB, Chauvel P, Liégeois-Chauvel C. Identification reaction times of voiced/voiceless continua: a rigjt-er advantage for VOT values near the phonetic boundary. Brain Lang 2000; 75: 153–62
   PubMed Web of Science ®Google Scholar