Plasticity and Restoration after Visual System Damage: Clinical Applications of the “Residual Vision Activation Theory”

2013 ◽  
pp. 196-228
Author(s):  
Carolin Gall ◽  
Bernhard A. Sabel
1998 ◽  
Vol 4 (4) ◽  
pp. 227-230 ◽  
Author(s):  
Tirin Moore ◽  
Hillary R. Rodman ◽  
Charles G. Gross

The visual function that survives damage to the primary visual cortex (V1) in humans is often unaccompanied by awareness. This type of residual vision, called “blindsight,” has raised considerable interest because it implies a separation of conscious from unconscious vision mechanisms. The monkey visual system has proven to be a useful model in elucidating the possible neural mechanisms of residual vision and blindsight in humans. Clear similarities, however, between the phenomenology of human and monkey residual vision have only recently become evident. This article summarizes parallels between residual vision in monkeys and humans with damage to V1. These parallels Include the tendency of the remaining vision to require forced-choice testing and the fact that more robust residual vision remains when V1 damage is sustained early in life. NEUROSCIENTIST 4:227–230


2015 ◽  
Vol 28 (3-4) ◽  
pp. 309-330 ◽  
Author(s):  
Simona Turco ◽  
Simona Turco ◽  
Emilio Albamonte ◽  
Simona Turco ◽  
Emilio Albamonte ◽  
...  

This review has the purpose of retracing the work of Professor Bernard Sabel and his group over the last 2–3 decades, in order to understand how they achieved formulation of the ‘Residual Vision Activation Theory’. The methodology proposed is described, from the first studies in 1995 with High Resolution Perimetry requiring a six-months training period, to the new technologies, such as repetitive transorbital Alternating Current Stimulation, that require ten days of training. Vision restoration therapy has shown improvement in visual responses irrespective of age at the training, lesion aetiology and site of lesion. The hypothesis that visual training may induce network plasticity, improving neuronal networks in cortical and subcortical areas of both hemispheres, appears to be confirmed by recent studies including observation of the cerebral activity by fMRI and EEG. However, the results are quite variable and the mechanisms that influence cerebral activity are still unclear. The residual vision activation theory has been much criticized, both for its methodology and analysis of the results, but it gave a new impulse to the research in this area, stimulating more studies on induced cerebral plasticity.


Neurology ◽  
1991 ◽  
Vol 41 (6) ◽  
pp. 862-862 ◽  
Author(s):  
G. G. Celesia ◽  
D. Bushnell ◽  
S. C. Toleikis ◽  
M. G. Brigell

2020 ◽  
Author(s):  
Samson Chengetanai ◽  
Adhil Bhagwandin ◽  
Mads F. Bertelsen ◽  
Therese Hård ◽  
Patrick R. Hof ◽  
...  

Author(s):  
Klaus-Ruediger Peters

Differential hysteresis processing is a new image processing technology that provides a tool for the display of image data information at any level of differential contrast resolution. This includes the maximum contrast resolution of the acquisition system which may be 1,000-times higher than that of the visual system (16 bit versus 6 bit). All microscopes acquire high precision contrasts at a level of <0.01-25% of the acquisition range in 16-bit - 8-bit data, but these contrasts are mostly invisible or only partially visible even in conventionally enhanced images. The processing principle of the differential hysteresis tool is based on hysteresis properties of intensity variations within an image.Differential hysteresis image processing moves a cursor of selected intensity range (hysteresis range) along lines through the image data reading each successive pixel intensity. The midpoint of the cursor provides the output data. If the intensity value of the following pixel falls outside of the actual cursor endpoint values, then the cursor follows the data either with its top or with its bottom, but if the pixels' intensity value falls within the cursor range, then the cursor maintains its intensity value.


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