By Gastone Celesia
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Additional resources for Disorders of Peripheral and Central Auditory Processing
Interaural balance of excitation and inhibition) have been mapped in some detail. The boundaries of such modules may not be sharp, however, indicating a partial integration of afferent inputs from multiple sources. This convergence may be thought of as overlapping spatial distributions of receptive field properties with peak density at different points within a given lamina. 4. Binaural processing Binaural processing in the CNIC has attracted considerable attention. As described earlier, sound location is not an acoustic property mapped upon the cochlear receptors but the result of computational operations first occurring in different brainstem nuclei.
4. Nuclei of the lateral lemniscus In non-primate mammals the nuclei of the lateral lemniscus may be subdivided into two anatomically and functionally distinct ventral (VNLL) and dorsal (DNLL) nuclei. The nuclei are less distinct in Old World monkeys, difficult to define in apes and considered the most poorly elaborated part of the human auditory brainstem (JK Moore, 1987). 1. Ventral nucleus of the lateral lemniscus The VNLL in many mammals may be considered a nuclear complex with several subdivisions based on cytoarchitectonic and connectivity studies; no such divisions have been reported in humans.
Neurons of the dorsal cortex are broadly tuned, like those of the lateral cortex, and they are particularly sensitive to vocalizations. Dorsal cortex appears related to a commissural zone, which represents a transition between the tectum and midbrain tegmentum and contains neurons whose dendrites either run parallel to the path of IC commissural fibers or nearly at right angles to these axons. Neurons of the midbrain tegmentum, unlike tectal neurons, are characterized by relatively few, long, slender, straight, infrequently branched dendrites without prominent spines or appendages.
Disorders of Peripheral and Central Auditory Processing by Gastone Celesia