Reduction or Augmentation? why We need Two “Planks” before Deciding

1974 ◽  
Vol 39 (1) ◽  
pp. 460-462 ◽  
Author(s):  
Asenath Petrie

This note concentrates on two developments since the experimentally based concepts of the reducer and augmenter were introduced a decade and a half ago by Petrie and colleagues (5). These two are chosen because they emphasize how obsolete is the proposal of Baker, et al. that we discard the data from the second session of the investigation in determining the perceptual characteristics of juvenile delinquents. (1) An atypical perceptual modulation pattern occurs in adults with known abnormalities of the nervous system. A considerable number of juvenile delinquents present the same atypical ‘stimulus-governed’ pattern. The only way to date of identifying the stimulus-governed person, who differs in important ways from the rest of the population, is by having his performance from two sessions to allow for comparison. The stimulus-governed person is wrongly characterized on one session alone. (2) The neurophysiological finding that augmenters have larger cortical-evoked responses than have reducers is based on measurements combining the information from two sessions. Other spinal neurophysiological correlates are similarly based. Thus, the bridge between reduction and augmentation on a perceptual level and these neurophysiological correlates was built on two ‘planks.’ The economy of discarding one of these planks, as suggested by Baker, et al., would prevent our using this vital bridge.

Planta Medica ◽  
2015 ◽  
Vol 81 (11) ◽  
Author(s):  
J Zhang ◽  
Z Yang ◽  
Y Zhu ◽  
L Wang ◽  
J Wang ◽  
...  

Author(s):  
Konstantin Gulyabin

Mills' syndrome is a rare neurological disorder. Its nosological nature is currently not completely determined. Nevertheless, Mills' syndrome is considered to be a rare variant of the degenerative pathology of the central nervous system – a variant of focal cortical atrophy. The true prevalence of this pathology is unknown, since this condition is more often of a syndrome type, observed in the clinical picture of a number of neurological diseases (primary lateral sclerosis, frontotemporal dementia, etc.) and is less common in isolated form.


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