Research paperGenerators of the brainstem auditory evoked potential in cat. II. Correlating lesion sites with waveform changes☆
References (46)
- et al.
Auditory brain stem responses in the cat. II. Effects of lesions
Electroenceph. Clin. Neurophysiol.
(1980) - et al.
Functional damage of dopamine nerve terminals following intrastriatal kainic acid injection
Brain Res.
(1989) - et al.
The effect of inferior colliculus lesions on auditory evoked potentials
Electroenceph. Clin. Neurophysiol.
(1987) - et al.
The effect of brainstem lesions on brainstem auditory evoked potentials in the cat
Hear. Res.
(1990) - et al.
The use of kainic acid for studying the origins of scalp-recorded auditory brainstem responses in the guinea pig
Neurosci. Lett.
(1981) - et al.
Kainic acid-induced terminal degeneration in the dorsal lateral geniculate of tree shrew
Brain Res.
(1987) - et al.
Is there a selectivity of neuronal degeneration induced by intrastrial injection of kainic acid?
Brain Res.
(1979) - et al.
Histofluorescence of kainic acid-induced striatal lesions
Brain Res.
(1978) - et al.
Generators of the brainstem auditory evoked potential in cat. III. Identified cell populations
Hear. Res.
(1996) - et al.
Generators of the brainstem auditory evoked potential in cat. I. An experimental approach to their identification
Hear. Res.
(1996)
Same location of the source of P1 of BAEPs and N1 of CAP in guinea pig
Hear. Res.
Effects of myelin or cell body brainstem lesions on 3-channel Lissajous' trajectories of feline auditory brainstem evoked potentials
Hear. Res.
Intra- and extracranially recorded auditory evoked potentials in the cat. II. Effects of interaural time and intensity differences
Electroenceph. Clin. Neurophysiol.
Eighth nerve contributions to the cat auditory brainstem responses (ABR)
Hear. Res.
The neuronal architecture of the anteroventral cochlear nucleus of the cat in the region of the cochlear nerve root: horseradish peroxidase labelling of identified cell types
Neuroscience
Anterograde transport of horseradish peroxidase in the nigrostriatal pathway after neostriatal kainic acid
Exp. Neurol.
A histological study of kainic acid-induced lesions in the rat brain
Brain Res.
Auditory brain-stem evoked potentials in cat after kainic acid induced neuronal loss. I. Superior olivary complex
Electroenceph. Clin. Neurophysiol.
Auditory brain-stem evoked potentials in cat after kainic acid induced neuronal loss. II. Cochlear nucleus
Electroenceph. Clin. Neurophysiol.
Long-term sequelae of striatal kainate lesion
Brain Res.
Ascending projections to the inferior colliculus
J. Comp. Neurol.
The neuronal architecture of the cochlear nucleus of the cat
J. Comp. Neurol.
Neural generators of brainstem auditory evoked responses. Part I. Lesion studies
Soc. Neurosci. Abstr.
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2021, Progress in Brain ResearchPaired measurements of cochlear function and hair cell count in Dutch-belted rabbits with noise-induced hearing loss
2020, Hearing ResearchCitation Excerpt :We repeatedly observed Waves I, II, IV and V in click-evoked ABR waveforms of our Dutch-belted rabbits, with Wave III most often obscured, whereas Stieve et al. (2006) most often observed Waves I–IV in New Zealand rabbits, with Wave V often unobservable. In both strains of rabbit, peak amplitude decreased with wave number—a pattern similar to mice (Zhou et al., 2006), cats (Melcher et al., 1996), guinea pigs (Wada and Starr, 1983), and chinchillas (Henry et al., 2011), but in contrast to humans, in which the amplitude of Wave V is larger than that of Wave I (Verhulst et al., 2016). In contrast to our finding that the variability of peak latency increased with wave number in Dutch-belted rabbits, Stieve et al. (2006) found constant, very low variability of peak latency across wave number in New Zealand rabbits, potentially due to their use of a higher-level click to evoke the ABR.
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Portions of this work were presented at the Annual Meeting of the Society for Neuroscience (1990), at the Annual Midwinter Meeting of the Association for Research in Otolaryngology (1993), and in J.R.M.'s doctoral thesis (Massachusetts Institute of Technology, Boston, MA, 1993).