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Title of Journal: J Comput Neurosci

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Abbravation: Journal of Computational Neuroscience

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Springer US

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DOI

10.1016/0145-305x(81)90011-2

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1573-6873

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Automatic classification and robust identification

Authors: Atiyeh Ghoreyshi Henrietta Galiana
Publish Date: 2011/01/20
Volume: 31, Issue: 2, Pages: 347-368
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Abstract

The VestibuloOcular Reflex VOR stabilizes images of the world on our retinae when our head moves Basic daily activities are thus impaired if this reflex malfunctions During the past few decades scientists have modeled and identified this system mathematically to diagnose and treat VOR deficits However traditional methods do not analyze VOR data comprehensively because they disregard the switching nature of nystagmus this can bias estimates of VOR dynamics Here we propose for the first time an automated tool to analyze entire VOR responses slow and fast phases without a priori classification of nystagmus segments We have developed GNLHybELS Generalized NonLinear Hybrid Extended Least Squares an algorithmic tool to simultaneously classify and identify the responses of a multimode nonlinear system with delay such as the horizontal VOR and its alternating slow and fast phases This algorithm combines the procedures of Generalized Principle Component Analysis GPCA for classification and Hybrid Extended Least Squares HybELS for identification by minimizing a cost function in an optimization framework It is validated here on clean and noisy VOR simulations and then applied to clinical VOR tests on controls and patients Prediction errors were less than 1 deg for simulations and ranged from 69 deg to 21 deg for the clinical data Nonlinearities asymmetries and dynamic parameters were detected in normal and patient data in both fast and slow phases of the response This objective approach to VOR analysis now allows the design of more complex protocols for the testing of oculomotor and other hybrid systemsThis work was supported by a Discovery Grant from the Natural Sciences and Engineering Council NSERC Canada and the Canadian Institutes for Health Research CIHR Canada The authors are grateful to Dr A Katasarkas for his help in selecting and recruiting patient participation and to HL Smith for her assistance during clinical recordings


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  1. Arousal increases the representational capacity of cortical tissue
  2. Modelling zinc changes at the hippocampal mossy fiber synaptic cleft
  3. Increased bradykinesia in Parkinson’s disease with increased movement complexity: elbow flexion–extension movements
  4. Loss of phase-locking in non-weakly coupled inhibitory networks of type-I model neurons
  5. Models of passive and active dendrite motoneuron pools and their differences in muscle force control
  6. Energy-based stochastic control of neural mass models suggests time-varying effective connectivity in the resting state
  7. Initiation and propagation of a neuronal intracellular calcium wave
  8. Two’s company, three (or more) is a simplex
  9. A simple Markov model of sodium channels with a dynamic threshold
  10. Can homeostatic plasticity in deafferented primary auditory cortex lead to travelling waves of excitation?
  11. A novel approach to the detection of synchronisation in EEG based on empirical mode decomposition
  12. Finite-size and correlation-induced effects in mean-field dynamics
  13. Synchronization of delayed coupled neurons in presence of inhomogeneity
  14. Stimulation-induced ectopicity and propagation windows in model damaged axons
  15. Neural coding of categories: information efficiency and optimal population codes
  16. Hallucinogen persisting perception disorder in neuronal networks with adaptation
  17. The relationship between nernst equilibrium variability and the multifractality of interspike intervals in the hippocampus
  18. A new 3D mass diffusion–reaction model in the neuromuscular junction
  19. How the cortico-thalamic feedback affects the EEG power spectrum over frontal and occipital regions during propofol-induced sedation
  20. Local cortical circuit model inferred from power-law distributed neuronal avalanches

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