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1 | (10) |
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1 | (1) |
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2 | (3) |
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The approaches taken to emotion and motivation |
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5 | (2) |
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7 | (3) |
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10 | (31) |
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10 | (1) |
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11 | (2) |
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13 | (8) |
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Refinements of the theory of emotion |
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21 | (4) |
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The classification of emotion |
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25 | (1) |
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Other theories of emotion |
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26 | (6) |
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The James-Lange and other bodily theories |
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26 | (4) |
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30 | (1) |
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Dimensional and categorical theories of emotion |
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31 | (1) |
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Other approaches to emotion |
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31 | (1) |
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Individual differences in emotion, personality, and emotional intelligence |
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32 | (3) |
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35 | (1) |
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Emotion, motivation, reward, and mood |
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36 | (1) |
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37 | (1) |
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Advantages of the approach to emotion described here (Rolls' theory of emotion) |
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38 | (3) |
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The functions of emotion: reward, punishment, and emotion in brain design |
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41 | (22) |
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41 | (2) |
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Brain design and the functions of emotion |
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43 | (6) |
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Taxes, rewards, and punishers: gene-specified goals for actions, and the flexibility of actions |
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43 | (4) |
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Explicit systems, language, and reinforcement |
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47 | (1) |
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Special-purpose design by an external agent vs evolution by natural selection |
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48 | (1) |
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Selection of behaviour: cost--benefit `analysis' |
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49 | (2) |
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Further functions of emotion |
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51 | (10) |
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Autonomic and endocrine responses |
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51 | (1) |
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Flexibility of behavioural responses |
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52 | (1) |
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Emotional states are motivating |
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53 | (1) |
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54 | (3) |
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57 | (1) |
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Separate functions for each different primary reinforcer |
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57 | (1) |
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The mood state can influence the cognitive evaluation of moods or memories |
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58 | (1) |
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Facilitation of memory storage |
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58 | (1) |
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Emotional and mood states are persistent, and help to produce persistent motivation |
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59 | (1) |
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Emotions may trigger memory recall and influence cognitive processing |
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59 | (2) |
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The functions of emotion in an evolutionary, Darwinian, context |
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61 | (1) |
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The functions of motivation in an evolutionary, Darwinian, context |
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61 | (1) |
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Are all goals for action gene-specified? |
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62 | (1) |
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The brain mechanisms underlying emotion |
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63 | (158) |
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63 | (1) |
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63 | (3) |
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Representations of primary reinforcers |
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66 | (5) |
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67 | (1) |
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67 | (1) |
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Pleasant and painful touch |
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67 | (2) |
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69 | (2) |
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Representing potential secondary reinforcers |
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71 | (20) |
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The requirements of the representation |
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71 | (3) |
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74 | (1) |
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Objects, and not their reward and punishment associations, are represented in the inferior temporal visual cortex |
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75 | (2) |
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77 | (1) |
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Invariant representations of faces and objects in the inferior temporal visual cortex |
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78 | (11) |
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Face expression, gesture and view represented in a population of neurons in the cortex in the superior temporal sulcus |
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89 | (1) |
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The brain mechanisms that build the appropriate view-invariant representations of objects required for learning emotional responses to objects, including faces |
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89 | (2) |
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91 | (58) |
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91 | (1) |
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92 | (1) |
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93 | (2) |
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Effects of damage to the orbitofrontal cortex |
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95 | (2) |
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Neurophysiology and functional neuroimaging of the orbitofrontal cortex |
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97 | (34) |
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The human orbitofrontal cortex |
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131 | (9) |
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A neurophysiological and computational basis for stimulus--reinforcer association learning and reversal in the orbitofrontal cortex |
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140 | (7) |
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Executive functions of the orbitofrontal cortex |
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147 | (2) |
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149 | (30) |
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Associative processes involved in emotion-related learning |
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149 | (6) |
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Connections of the amygdala |
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155 | (2) |
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Effects of amygdala lesions |
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157 | (7) |
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Neuronal activity in the primate amygdala to reinforcing stimuli |
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164 | (6) |
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Responses of these amygdala neurons to novel stimuli that are reinforcing |
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170 | (2) |
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Neuronal responses in the amygdala to faces |
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172 | (3) |
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175 | (3) |
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178 | (1) |
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179 | (8) |
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Perigenual cingulate cortex and affect |
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181 | (4) |
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Mid-cingulate cortex, the cingulate motor area, and action--outcome learning |
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185 | (2) |
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Human brain imaging investigations of mood and depression |
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187 | (1) |
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Output pathways for emotional responses |
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188 | (6) |
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The autonomic and endocrine systems |
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188 | (1) |
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Motor systems for implicit responses, including the basal ganglia |
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189 | (1) |
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Output systems for explicit responses to emotional stimuli |
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190 | (1) |
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Basal forebrain and hypothalamus |
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191 | (1) |
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Basal forebrain cholinergic neurons |
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191 | (3) |
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194 | (1) |
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Effects of emotion on cognitive processing and memory |
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194 | (6) |
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Laterality effects in human emotional processing |
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200 | (2) |
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202 | (3) |
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205 | (16) |
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221 | (53) |
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221 | (1) |
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Peripheral signals for hunger and satiety |
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221 | (3) |
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The control signals for hunger and satiety |
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224 | (9) |
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224 | (6) |
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230 | (1) |
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230 | (1) |
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230 | (1) |
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Body fat regulation -- leptin or OB protein |
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231 | (1) |
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Conditioned appetite and satiety |
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232 | (1) |
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The brain control of eating and reward |
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233 | (38) |
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233 | (10) |
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Brain mechanisms for the reward produced by the taste of food |
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243 | (10) |
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Convergence between taste and olfactory processing to represent flavour |
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253 | (1) |
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Brain mechanisms for the reward produced by the odour of food |
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254 | (5) |
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The responses of orbitofrontal cortex taste and olfactory neurons to the sight of food |
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259 | (1) |
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Functions of the amygdala and temporal cortex in feeding |
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259 | (4) |
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Functions of the orbitofrontal cortex in feeding |
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263 | (3) |
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Functions of the striatum in feeding |
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266 | (5) |
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Obesity, bulimia, and anorexia |
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271 | (2) |
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Conclusions on reward, affective responses to food, and the control of appetite |
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273 | (1) |
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274 | (14) |
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274 | (1) |
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Cellular stimuli for drinking |
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275 | (1) |
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Extracellular thirst stimuli |
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276 | (3) |
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Extracellular stimuli for thirst |
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276 | (2) |
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Role of the kidney in extracellular thirst: the renin--angiotensin system |
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278 | (1) |
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Cardiac receptors for thirst |
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279 | (1) |
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Control of normal drinking |
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279 | (3) |
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Reward and satiety signals for drinking |
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282 | (4) |
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286 | (2) |
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288 | (20) |
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288 | (1) |
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The nature of the reward produced |
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288 | (4) |
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The location of brain-stimulation reward sites in the brain |
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292 | (1) |
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The effects of brain lesions on intracranial self-stimulation |
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293 | (1) |
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The neurophysiology of reward |
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294 | (6) |
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Lateral hypothalamus and substantia innominata |
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294 | (2) |
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296 | (2) |
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298 | (1) |
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299 | (1) |
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Central gray of the midbrain |
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299 | (1) |
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Some of the properties of brain-stimulation reward |
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300 | (4) |
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Lack of satiety with brain-stimulation reward |
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300 | (2) |
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302 | (1) |
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302 | (2) |
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Stimulus-bound motivational behaviour |
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304 | (1) |
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305 | (1) |
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306 | (2) |
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Pharmacology of emotion, reward, and addiction; the basal ganglia |
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308 | (50) |
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308 | (3) |
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The noradrenergic hypothesis |
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311 | (1) |
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312 | (9) |
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Dopamine and electrical self-stimulation of the brain |
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312 | (2) |
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Self-administration of dopaminergic substances, and addiction |
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314 | (2) |
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Behaviours associated with the release of dopamine |
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316 | (2) |
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The activity of dopaminergic neurons and reward |
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318 | (3) |
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321 | (31) |
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Systems-level architecture of the basal ganglia |
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322 | (1) |
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Effects of basal ganglia damage |
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323 | (2) |
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Neuronal activity in the striatum |
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325 | (14) |
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What computations are performed by the basal ganglia? |
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339 | (1) |
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How do the basal ganglia perform their computations? |
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340 | (8) |
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Synthesis on the role of dopamine in reward and addiction |
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348 | (2) |
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Synthesis: emotion, dopamine, reward, punishment, and action selection in the basal ganglia |
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350 | (2) |
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Opiate reward systems, analgesia, and food reward |
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352 | (1) |
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Pharmacology of depression in relation to brain systems involved in emotion |
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353 | (1) |
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Pharmacology of anxiety in relation to brain systems involved in emotion |
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354 | (1) |
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355 | (1) |
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Overview of behavioural selection and output systems involved in emotion |
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355 | (3) |
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Sexual behaviour, reward, and brain function; sexual selection of behaviour |
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358 | (42) |
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358 | (2) |
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Mate selection, attractiveness, and love |
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360 | (7) |
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361 | (2) |
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363 | (3) |
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366 | (1) |
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Parental attachment, care, and parent--offspring conflict |
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367 | (1) |
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Sperm competition and its consequences for sexual behaviour |
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368 | (7) |
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Concealed ovulation and its consequences for sexual behaviour |
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375 | (1) |
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Sexual selection of sexual and non-sexual behaviour |
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376 | (5) |
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Sexual selection and natural selection |
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376 | (3) |
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Non-sexual characteristics may be sexually selected for courtship |
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379 | (2) |
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Individual differences in sexual rewards |
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381 | (6) |
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381 | (3) |
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How might different types of behaviour be produced by natural selection altering the relative reward value of different stimuli in different individuals? |
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384 | (2) |
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How being tuned to different types of reward could help to produce individual differences in sexual behaviour |
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386 | (1) |
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The neural reward mechanisms that might mediate some aspects of sexual behaviour |
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387 | (8) |
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Neural basis of sexual behaviour |
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395 | (3) |
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398 | (2) |
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Emotional feelings and consciousness: a theory of consciousness |
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400 | (26) |
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400 | (1) |
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A theory of consciousness |
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401 | (10) |
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411 | (7) |
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Content and meaning in representations |
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418 | (2) |
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420 | (3) |
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Conclusions and comparisons |
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423 | (3) |
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Conclusions, and broader issues |
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426 | (28) |
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426 | (5) |
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431 | (14) |
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Selection of mainly autonomic responses, and their classical conditioning |
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431 | (1) |
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Selection of approach or withdrawal, and their classical conditioning |
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431 | (1) |
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Selection of fixed stimulus--response habits |
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432 | (1) |
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Selection of arbitrary behaviours to obtain goals, action--outcome learning, and emotional learning |
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432 | (1) |
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The roles of the prefrontal cortex in decision-making and attention |
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433 | (7) |
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Neuroeconomics, reward value, and expected utility |
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440 | (4) |
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Selection of actions by explicit rational thought |
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444 | (1) |
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445 | (4) |
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449 | (3) |
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452 | (2) |
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A. Neural networks and emotion-related learning |
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454 | (47) |
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Neurons in the brain, the representation of information, and neuronal learning mechanisms |
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454 | (12) |
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454 | (1) |
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Neurons in the brain, and their representation in neuronal networks |
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454 | (2) |
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A formalism for approaching the operation of single neurons in a network |
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456 | (2) |
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458 | (1) |
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Long-Term Potentiation and Long-Term Depression |
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459 | (5) |
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Distributed representations |
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464 | (2) |
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Pattern association memory |
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466 | (17) |
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Architecture and operation |
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466 | (3) |
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469 | (3) |
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The vector interpretation |
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472 | (1) |
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472 | (3) |
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Prototype extraction, extraction of central tendency, and noise reduction |
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475 | (1) |
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475 | (1) |
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476 | (6) |
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Implications of different types of coding for storage in pattern associators |
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482 | (1) |
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Autoassociation memory: attractor networks |
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483 | (8) |
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Architecture and operation |
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483 | (2) |
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Introduction to the analysis of the operation of autoassociation networks |
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485 | (1) |
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486 | (5) |
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Coupled attractor networks |
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491 | (2) |
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493 | (8) |
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Associative reward--penalty algorithm of Barto and Sutton |
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494 | (2) |
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Error correction or delta rule learning, and classical conditioning |
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496 | (1) |
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Temporal Difference (TD) learning |
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497 | (4) |
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B. Reward reversal in the orbitofrontal cortex -- a model |
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501 | (24) |
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501 | (2) |
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The model of stimulus--reinforcer association reversal |
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503 | (8) |
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504 | (3) |
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Reward reversal: the operation of the rule module neurons |
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507 | (2) |
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509 | (1) |
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The synapses in the model |
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510 | (1) |
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Operation of the reward reversal model |
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511 | (4) |
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A model of reversal of a conditional object-response task by the dorsolateral prefrontal cortex |
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515 | (2) |
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517 | (4) |
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Integrate-and-Fire model equations and parameters |
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521 | (1) |
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Simulation of fMRI signals: haemodynamic convolution of synaptic activity |
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522 | (3) |
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525 | (3) |
References |
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528 | (74) |
Index |
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602 | |