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Preface |
7 |
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Contents |
10 |
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List of Contributors |
13 |
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Part I Data Mining |
19 |
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1 Optimization in Reproducing Kernel Hilbert Spacesof Spike Trains |
20 |
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1.1 Introduction |
21 |
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1.2 Some Background on RKHS Theory |
22 |
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1.3 Inner Product for Spike Times |
24 |
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1.4 Inner Product for Spike Trains |
25 |
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1.5 Properties and Estimation of the Memoryless Cross-Intensity Kernel |
27 |
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1.5.1 Properties |
27 |
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1.5.2 Estimation |
29 |
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1.6 Induced RKHS and Congruent Spaces |
30 |
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1.6.1 Space Spanned by Intensity Functions |
31 |
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1.6.2 Induced RKHS |
31 |
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1.6.3 mCI Kernel and the RKHS Induced by |
32 |
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1.6.4 mCI Kernel as a Covariance Kernel |
33 |
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1.7 Principal Component Analysis |
34 |
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1.7.1 Optimization in the RKHS |
34 |
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1.7.2 Optimization in the Space Spanned by the Intensity Functions |
37 |
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1.7.3 Results |
38 |
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1.8 Conclusion |
42 |
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References |
44 |
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2 Investigating Functional Cooperation in the Human Brain Using Simple Graph-Theoretic Methods |
47 |
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2.1 Introduction and Background |
47 |
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2.2 Graph Theory and Neuroscience |
49 |
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2.3 A Database of Imaging Experiments |
51 |
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2.4 The Usefulness of Co-activation Graphs |
53 |
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2.5 Relating fMRI to EEG |
55 |
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2.6 Conclusion |
57 |
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References |
57 |
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3 Methodological Framework for EEG Feature Selection Based on Spectral and Temporal Profiles |
59 |
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3.1 Introduction |
60 |
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3.2 Methods |
61 |
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3.2.1 Methodology Overview |
61 |
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3.2.2 Feature Extraction (Step 1) |
62 |
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3.2.3 Feature Selection (Step 2) |
66 |
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3.2.4 Feature Refinement (Steps 3 and 4) |
66 |
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3.3 Results |
68 |
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3.3.1 Simulation Test |
68 |
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3.4 Discussion |
69 |
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3.5 Conclusion |
70 |
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References |
71 |
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4 Blind Source Separation of Concurrent Disease-Related Patterns from EEG in Creutzfeldt--Jakob Disease for Assisting Early Diagnosis |
73 |
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4.1 Introduction |
74 |
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4.2 Patients and EEG Recordings |
78 |
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4.3 Methods |
80 |
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4.3.1 Independent Component Analysis and Extractionof CJD-Related Components |
80 |
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4.3.2 Bayesian Information Criterion |
81 |
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4.4 Results |
82 |
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4.4.1 Determination of the Number of Sources |
82 |
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4.4.2 CJD-Related Feature Extraction |
83 |
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4.4.3 Feature Extraction by PCA |
85 |
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4.5 Discussions |
85 |
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4.6 Conclusions |
88 |
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References |
89 |
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5 Comparison of Supervised Classification Methods with Various Data Preprocessing Procedures for Activation Detectionin fMRI Data |
91 |
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5.1 Introduction |
91 |
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5.2 Data Set |
92 |
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5.3 Data Preprocessing |
93 |
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5.4 Pattern Recognition Methods |
94 |
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5.4.1 Fisher Linear Discriminant |
95 |
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5.4.2 Support Vector Machine |
95 |
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5.4.3 Gaussian Nave Bayes |
96 |
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5.4.4 Correlation Analysis |
96 |
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5.4.5 k-Nearest Neighbor |
96 |
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5.5 Results |
97 |
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5.6 Conclusions |
98 |
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References |
98 |
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6 Recent Advances of Data Biclustering with Application in Computational Neuroscience |
100 |
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6.1 Introduction |
100 |
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6.1.1 Motivation |
100 |
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6.1.2 Data Input |
101 |
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6.1.3 Objective of Task |
102 |
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6.1.4 History |
103 |
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6.1.5 Outline |
104 |
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6.2 Biclustering Types and Structures |
104 |
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6.2.1 Notations |
104 |
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6.2.2 Bicluster Types |
105 |
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6.2.3 Biclustering Structures |
107 |
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6.3 Biclustering Techniques and Algorithms |
109 |
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6.3.1 Based on Matrix Means and Residues |
109 |
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6.3.2 Based on Matrix Ordering, Reordering, and Decomposition |
111 |
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6.3.3 Based on Bipartite Graphs |
115 |
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6.3.4 Based on Information Theory |
118 |
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6.3.5 Based on Probability |
119 |
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6.3.6 Comparison of Biclustering Algorithms |
121 |
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6.4 Application of Biclustering in Computational Neuroscience |
122 |
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6.5 Conclusions |
124 |
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References |
124 |
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7 A Genetic Classifier Account for the Regulation of Expression |
128 |
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7.1 Introduction |
128 |
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7.1.1 Motivation |
128 |
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7.1.2 Background |
129 |
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7.2 Model and Methods |
130 |
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7.2.1 Basic Assumptions |
130 |
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7.2.2 Model Structure |
130 |
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7.2.3 Model Equations |
131 |
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7.2.4 Stability |
132 |
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7.3 Results |
132 |
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7.3.1 Composition by Overlap of Nodes |
132 |
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7.3.1.1 Complete Overlap |
132 |
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7.3.1.2 Incomplete Overlap |
134 |
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7.3.2 Multiple Gene Scenarios |
134 |
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7.3.2.1 Three Genes |
134 |
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7.3.3 Composition by Infinite Chains |
135 |
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7.3.3.1 Chain of Genes Including A 1-Product Gene |
136 |
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7.3.3.2 Chain of Genes Without A 1-Product Gene |
136 |
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7.3.4 Subchains |
137 |
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7.4 Discussion |
137 |
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References |
138 |
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Part II Modeling |
139 |
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8 Neuroelectromagnetic Source Imaging of Brain Dynamics |
140 |
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8.1 Introduction |
140 |
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8.1.1 Neuronal Origins of Electromagnetic Signals |
141 |
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8.2 Measurement Modalities |
142 |
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8.2.1 Magnetoencephalography (MEG) |
142 |
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8.2.2 Electroencephalography (EEG) |
143 |
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8.2.3 Electrocorticography (ECoG) |
143 |
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8.3 Data Preprocessing |
143 |
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8.4 Overview of Modeling Steps |
145 |
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8.4.1 Modeling of Neural Generators |
145 |
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8.4.2 Anatomical Modeling of Head Tissues and Neural Sources |
146 |
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8.4.3 Multimodal Geometric Registration |
146 |
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8.4.4 Forward Modeling |
147 |
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8.4.5 Inverse Modeling |
147 |
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8.5 Parametric Dipole Modeling |
148 |
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8.5.1 Uncorrelated Noise Model |
148 |
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8.5.2 Correlated Noise Model |
149 |
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8.5.3 Global Minimization |
150 |
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8.6 Source Space-Based Distributed and Sparse Methods |
150 |
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8.6.1 Bayesian Maximum a Posteriori (MAP) Estimates |
151 |
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8.6.2 Dynamic Statistical Parametric Mapping (dSPM) |
154 |
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8.6.3 Standardized Low Resolution Brain Electromagnetic Tomography (sLORETA) |
155 |
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8.6.4 Sparse Bayesian Learning (SBL) and Automatic Relevance Determination (ARD) |
156 |
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8.7 Spatial Scanning and Beamforming |
158 |
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8.7.1 Matched Filter |
159 |
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8.7.2 Multiple Signal Classification (MUSIC) |
159 |
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8.7.3 Linearly Constrained Minimum Variance (LCMV) Beamforming |
160 |
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8.7.4 Synthetic Aperture Magnetometry (SAM) |
160 |
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8.7.5 Dynamic Imaging of Coherent Sources (DICS) |
161 |
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8.7.6 Other Spatial Filtering Methods |
161 |
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8.8 Comparison of Methods |
162 |
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8.9 Conclusion |
162 |
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References |
164 |
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9 Optimization in Brain? -- Modeling Human Behavior and Brain Activation Patterns with Queuing Network and Reinforcement Learning Algorithms |
169 |
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9.1 Introduction |
169 |
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9.2 Modeling Behavioral and Brain Imaging Phenomena in Transcription Typing with Queuing Networks and Reinforcement Learning Algorithms |
171 |
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9.2.1 Behavioral Phenomena |
171 |
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9.2.2 Brain Imaging Phenomena |
171 |
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9.2.3 A Queuing Network Model with Reinforcement Learning Algorithms |
172 |
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9.2.3.1 The Static Portion of the Queuing Network Model |
172 |
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9.2.3.2 The Dynamic Portion of the Queuing Network Model: Self-Organization of the Queuing Network with Reinforcement Learning Algorithms |
173 |
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9.2.4 Model Predictions of three Skill Learning Phenomenaand two Brain Imaging Phenomena |
176 |
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9.2.4.1 Predictions of the three Skill Learning Phenomena |
176 |
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9.2.4.2 Predictions of the First Brain Imaging Phenomenon |
177 |
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9.2.4.3 Predictions of the Second Brain Imaging Phenomenon |
177 |
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9.2.5 Simulation of the three Skill Learning Phenomenaand the two Brain Imaging Phenomena |
178 |
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9.2.5.1 The First and the Second Skill Learning Phenomena |
178 |
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9.2.5.2 The Third Skill Learning Phenomena |
178 |
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9.2.5.3 The First Brain Imaging Phenomena |
179 |
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9.2.5.4 The Second Brain Imaging Phenomena |
179 |
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9.3 Modeling the Basic PRP and Practice Effect on PRP with Queuing Networks and Reinforcement Learning Algorithms |
180 |
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9.3.1 Modeling the Basic PRP and the Practice Effect on PRPwith Queuing Networks |
180 |
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9.3.1.1 Learning Process in Individual Servers |
182 |
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9.3.1.2 Learning Process in the Simplest Queuing Network with two Routes |
183 |
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9.3.2 Predictions of the Basic PRP and the Practice Effect on PRP with the Queuing Network Model |
184 |
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9.3.3 Simulation Results |
184 |
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9.4 Discussion |
186 |
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References |
189 |
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10 Neural Network Modeling of Voluntary Single-Joint Movement Organization I. Normal Conditions |
192 |
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10.1 Introduction |
192 |
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10.2 Models and Theories of Motor Control |
193 |
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10.3 The Extended VITE--FLETE Models Without Dopamine |
195 |
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10.4 Conclusion |
200 |
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References |
200 |
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11 Neural Network Modeling of Voluntary Single-Joint Movement Organization II. Parkinson's Disease |
203 |
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11.1 Introduction |
203 |
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11.2 Brain Anatomy in Parkinson's Disease |
204 |
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11.3 Empirical Signatures |
206 |
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11.4 Is There Dopaminergic Innervation of the Cortexand Spinal Cord? |
206 |
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11.5 Effects of Dopamine Depletion on Neuronal, Electromyographic, and Movement Parameters in PD Humans and MPTP Animals |
207 |
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11.5.1 Cellular Disorganization in Cortex |
207 |
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11.5.2 Reduction of Neuronal Intensity and of Rate of Development of Neuronal Discharge in the PrimaryMotor Cortex |
208 |
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11.5.3 Significant Increase in Mean Duration of Neuronal Discharge in Primary Motor Cortex Preceding and Following Onset of Movement |
208 |
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11.5.4 Prolongation of Behavioral Simple Reaction Time |
209 |
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11.5.5 Repetitive Triphasic Pattern of Muscle Activation |
210 |
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11.5.6 Electromechanical Delay Time Is Increased |
210 |
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11.5.7 Depression of Rate of Development and Peak Amplitudeof the First Agonist Burst of EMG Activity |
210 |
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11.5.8 Movement Time Is Significantly Increased |
211 |
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11.5.9 Reduction of Peak Velocity |
212 |
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11.5.10 Reduction of Peak Force and Rate of Force Production |
212 |
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11.5.11 Movement Variability |
212 |
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11.6 The Extended VITE--FLETE Models with Dopamine |
213 |
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11.7 Simulated Effects of Dopamine Depletion on the Cortical Neural Activities |
216 |
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11.8 Simulated Effects of Dopamine Depletion on EMG Activities |
217 |
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11.9 Conclusion |
219 |
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References |
220 |
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12 Parametric Modeling Analysis of Optical Imaging Data on Neuronal Activities in the Brain |
223 |
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12.1 Introduction |
224 |
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12.2 Methods |
226 |
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12.2.1 Recording of Optical Signals and Preprocessing |
226 |
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12.2.2 Modeling |
228 |
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12.2.3 Classification of Optical Signals Based on Activation Timing |
229 |
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12.3 Results |
231 |
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12.3.1 Estimation of STF Model Parameters |
231 |
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12.3.2 Classification of Pixel Activity Patterns |
232 |
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12.4 Discussion |
234 |
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References |
234 |
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13 Advances Toward Closed-Loop Deep Brain Stimulation |
236 |
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13.1 Introduction |
236 |
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13.2 Nerve Stimulation |
237 |
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13.3 Local Field Potentials |
238 |
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13.4 Parkinson's Disease |
239 |
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13.4.1 Treatments |
240 |
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13.5 Deep Brain Stimulation |
241 |
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13.5.1 DBS Mechanism |
241 |
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13.5.2 Apparatus |
241 |
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13.5.3 Stimulus Specifications |
242 |
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13.5.4 DBS Programming |
244 |
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13.5.5 Side Effects |
246 |
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13.6 Biosignal Processing |
246 |
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13.6.1 Features |
247 |
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13.6.2 Classifiers |
247 |
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13.6.3 Feature Selection |
248 |
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13.7 Closed-Loop DBS |
248 |
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13.7.1 Demand-Controlled DBS |
249 |
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13.7.2 ALOPEX and DBS |
250 |
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13.7.3 Genetic Algorithms and DBS |
251 |
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13.7.4 Hardware Implementations |
251 |
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13.8 Related Advances in Other Neuroprosthetic Research |
252 |
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13.8.1 Closed-Loop Cardiac Pacemaker Technology |
253 |
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13.8.2 Brain-to-Computer Interface |
253 |
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13.9 Neural Network Modeling and the Basal Ganglia |
254 |
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13.10 Summary |
255 |
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References |
255 |
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14 Molecule-Inspired Methods for Coarse-Grain Multi-System Optimization |
263 |
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14.1 Introduction |
264 |
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14.2 Biomolecular Computing In Vitro |
265 |
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14.3 Biomolecular Computing In Silico |
266 |
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14.4 Neural Nets in Biomolecules |
268 |
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14.5 Conclusions and Future Work |
272 |
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References |
274 |
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Part III Brain Dynamics/Synchronization |
276 |
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15 A Robust Estimation of Information Flow in Coupled Nonlinear Systems |
277 |
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15.1 Introduction |
277 |
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15.2 Methodology |
279 |
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15.2.1 Transfer Entropy (TE) |
279 |
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15.2.2 Improved Computation of Transfer Entropy |
280 |
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15.2.2.1 Selection of k |
280 |
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15.2.2.2 Selection of l |
280 |
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15.2.2.3 Selection of Radius r |
281 |
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15.2.3 Statistical Significance of Transfer Entropy |
283 |
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15.2.4 Detecting Causality Using Transfer Entropy |
284 |
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15.3 Simulation Example |
284 |
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15.3.1 Statistical Significance of TE and NTE |
285 |
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15.3.2 Robustness to Noise |
287 |
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15.4 Discussion and Conclusion |
288 |
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References |
289 |
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16 An Optimization Approach for Finding a Spectrum of Lyapunov Exponents |
290 |
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16.1 Introduction |
290 |
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16.2 Lyapunov Exponents |
291 |
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16.3 An Optimization Approach |
293 |
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16.3.1 Theory |
294 |
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16.3.2 Implementation Details |
295 |
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16.3.2.1 Phase Space Reconstruction |
296 |
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16.4 Models Used in the Computational Experiments |
299 |
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16.4.1 Lorenz Attractor |
299 |
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16.4.2 Rössler Attractor |
300 |
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16.4.3 Hénon Map |
301 |
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16.4.4 The Hénon--Heiles Equations |
301 |
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16.5 Computational Experiments |
302 |
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16.5.1 Numerical Computations |
302 |
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16.5.2 Sensitivity Analysis |
304 |
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16.6 Summary and Conclusion |
306 |
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References |
306 |
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17 Dynamical Analysis of the EEG and Treatment of Human Status Epilepticus by Antiepileptic Drugs |
309 |
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17.1 Introduction |
310 |
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17.2 Materials and Methods |
311 |
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17.2.1 Recording Procedure and EEG Data |
311 |
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17.2.1.1 EEG from Barrow Neurological Institute, Phoenix, Arizona |
312 |
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17.2.1.2 EEG from Mayo Clinic Hospital, Scottsdale, Arizona |
312 |
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17.2.2 Measures of Brain Dynamics |
313 |
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17.2.2.1 Measure of Chaos(STLmax) |
313 |
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17.2.2.2 Measure of Dynamical Entrainment |
315 |
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17.3 Results |
315 |
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17.4 Conclusion |
317 |
|
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References |
318 |
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18 Analysis of Multichannel EEG Recordings Based on Generalized Phase Synchronization and Cointegrated VAR |
320 |
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18.1 Introduction |
320 |
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18.2 Integrated and Cointegrated VAR |
322 |
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18.2.1 Augmented Dickey--Fuller Test for Testing the Null Hypothesis of a Unit Root |
323 |
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18.2.2 Estimation of Cointegrated VAR(p) Processes |
325 |
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18.2.3 Testing for the Rank of Cointegration |
327 |
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18.3 The Role of Phase Synchronization in Neural Dynamics |
328 |
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18.4 Phase Estimation Using Hilbert Transform |
329 |
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18.5 Multivariate Approach to Phase Synchrony via Cointegrated VAR |
330 |
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18.5.1 Cointegration Rank as a Measure of Synchronization among Different EEG Channels |
331 |
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18.5.2 Absence Seizures |
334 |
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18.5.3 Numerical Study of Synchrony in Multichannel EEG Recordings from Patients with Absence Epilepsy |
334 |
|
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18.6 Conclusion |
338 |
|
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18.6.1 Phillips--Ouliaris Cointegration Test |
339 |
|
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References |
341 |
|
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19 Antiepileptic Therapy Reduces Coupling Strength Among Brain Cortical Regions in Patients with Unverricht--Lundborg Disease: A Pilot Study |
343 |
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19.1 Introduction |
344 |
|
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19.2 Data Information |
347 |
|
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19.3 Synchronization Measures |
348 |
|
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19.3.1 Mutual Information |
348 |
|
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19.3.2 Nonlinear Interdependencies |
350 |
|
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19.4 Statistical Tests and Data Analysis |
351 |
|
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19.5 Conclusion and Discussion |
354 |
|
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References |
355 |
|
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20 Seizure Monitoring and Alert System for Brain Monitoring in an Intensive Care Unit |
358 |
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20.1 Introduction |
359 |
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20.2 Preictal Transition and Seizure Prediction |
360 |
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20.3 Methods |
362 |
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20.3.1 Chaos Theory and Epilepsy |
362 |
|
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20.3.2 Statistical Method for Pairwise Comparison of STLMAX |
364 |
|
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20.3.3 Finding Critical Sites by Quadratic Optimization Approach |
365 |
|
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20.4 Two Main Components of the Seizure Monitoring and Alert System |
366 |
|
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20.4.1 Algorithm for Generating Automatic Warnings about Impending Seizure from EEG |
367 |
|
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20.5 Conclusions |
368 |
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References |
368 |
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