| Laureys & Tononi; Neurology of Consciousness | |||||
| (Table of Contents) | |||||
| Authors | Page | Topic | |||
| Damasio & Meyer; Consciousness Overview | 6 | Varieties of Consciousness | |||
| Damasio & Meyer; Consciousness Overview | 6 | Consciousness is a momentary creation of neural patterns, which describes a relation between the organism, on the one hand, and an object or event, on the other. | 0 | ||
| Damasio & Meyer; Consciousness Overview | 7 | Core consciousness is a prerequisite for the focusing and enhancement of attention and working memory; enables the establishment of explicit memories; is indispensable for language and normal communication; renders possible the intelligent manipulation of images (e.g., planning, problem solving, and creativity). | 1 | ||
| Damasio & Meyer; Consciousness Overview | 7 | Core consciousness is not based on language, is not equivalent to manipulating images in planning, problem solving, and creativity. | 0 | ||
| Damasio & Meyer; Consciousness Overview | 7 | Core consciousness depends on wakefulness. | 0 | ||
| Damasio & Meyer; Consciousness Overview | 7 | Varied cell groups in the brainstem modulate wakefulness by ascending projections to the cerebral cortex. | 0 | ||
| Damasio & Meyer; Consciousness Overview | 8 | Core Consciousness | 1 | ||
| Damasio & Meyer; Consciousness Overview | 8 | Extended Consciousness | 0 | ||
| Damasio & Meyer; Consciousness Overview | 9 | Extended consciousness requires working memory and explicit long-term memory (including both semantic and episodic memories). | 1 | ||
| Damasio & Meyer; Consciousness Overview | 12 | From an evolutionary perspective, core consciousness came to exist when second-order maps first brought together the representation of the organism modified by perceptual engagement with the representation of the object. | 3 | ||
| Laureys, et.al.; Functional Neuroimaging | 31 | Functional Neuroimaging | 19 | ||
| Singer; Neuronal Synchronization | 44 | The term 'consciousness' has a number of different connotations ranging from awareness of one's perceptions and sensations to self-awareness, the perception of oneself as a responsible agent that is endowed with intentionality and free will. | 13 | ||
| Singer; Neuronal Synchronization | 44 | Phenomenal awareness -- the ability to be aware of one's perceptions and intentions. | 0 | ||
| Singer; Neuronal Synchronization | 44 | Because sensory signals can be readily processed and influence motor responses without being consciously perceived, the cognitive operations leading to conscious experience are likely to differ from straightforward sensory-motor processing. | 0 | ||
| Singer; Neuronal Synchronization | 45 | One mechanism for dynamic binding is the precise synchronization of neuronal responses that occurs when neuronal populations engage in well synchronized oscillatory activity in the beta and gamma frequency range. | 1 | ||
| Singer; Neuronal Synchronization | 46 | Synchronized oscillations are strongly reduced or missing when the brain is in states that are incompatible with conscious processing. | 1 | ||
| Singer; Neuronal Synchronization | 47 | Attention related facilitation of synchronization. | 1 | ||
| Singer; Neuronal Synchronization | 48 | A close correlation between response synchronization and conscious perception has been found in experiments on binocular rivalry. | 1 | ||
| Singer; Neuronal Synchronization | 49 | Synchronization occurs in a variety of distinct frequency bands and has been found in all sensory modalities. | 1 | ||
| Singer; Neuronal Synchronization | 49 | Synchronization in the high frequency range (beta and gamma oscillations) has been observed in the olfactory system, and virtually all of the cortical areas, the hippocampus, and the basal ganglia. | 0 | ||
| Singer; Neuronal Synchronization | 49 | Synchronization also plays a role in the linkages between the cortical assemblies and subcortical target structures such is a superior colliculus in the pool of motor neurons in the spinal cord. | 0 | ||
| Singer; Neuronal Synchronization | 49 | The earliest event distinguishing conscious and unconscious processing is not the power changes of oscillations but in their phase locking. | 0 | ||
| Singer; Neuronal Synchronization | 49 | Local gamma oscillations had the same power in the conscious and unconscious condition. What distinguished these two conditions was the global synchronization of local gamma oscillations. | 0 | ||
| Singer; Neuronal Synchronization | 49 | Conscious processing requires a particular dynamical state of cortical networks that is characterized by a brief episode of very precise phase locking of high frequency oscillatory activity. | 0 | ||
| Singer; Neuronal Synchronization | 50 | An attractive hypothesis is that the transient event of perfect synchrony resets the multiple parallel processes to a common time frame, allowing for global integration and representation of information provided by sensory input and internal stores. | 1 | ||
| Singer; Neuronal Synchronization | 50 | The global theta rhythm that follows the triggering event could provide the timeframe for the integration. | 0 | ||
| Singer; Neuronal Synchronization | 50 | In the hippocampus and in the neocortex, slow oscillations in the theta range have been found to be coupled to the coexisting beta and gamma oscillations. | 0 | ||
| Singer; Neuronal Synchronization | 50 | It is hypothesized that a local coordination of computations within specific cortical areas is achieved by fast ticking clocks, such as beta and gamma oscillations, while global and sustained integration of local results is achieved at a slower pace by low-frequency oscillations in the theta range. | 0 | ||
| Singer; Neuronal Synchronization | 50 | These hypotheses would allow the brain to represent the results of numerous parallel computations at different temporal and spatial scales, whereby the two dimensions would be intimately related. | 0 | ||
| Singer; Neuronal Synchronization | 50 | The more global the representation, the longer the timescale for the integration of distributed information. | 0 | ||
| Singer; Neuronal Synchronization | 50 | It is perhaps more than mere coincidence that the duration of subjected presence corresponds approximately to the cycle time of theta rhythms. | 0 | ||
| Singer; Neuronal Synchronization | 50 | Consciousness appears to be an emergent property of a specific dynamical state of the cortical network -- a state that is characterized by a critical level of precise temporal coherence among responses of a sufficiently large population of distributed neurons. | 0 | ||
| Rees; Visual Consciousness | 53 | Neural Correlates of Visual Consciousness | 3 | ||
| Rees; Visual Consciousness | 55 | Binocular rivalry is a paradigm to study the neural correlates of consciousness. | 2 | ||
| Rees; Visual Consciousness | 55 | When dissimilar images are presented to the two eyes, they compete for perceptual dominance so that each image is visible in turn for a few seconds while the other is suppressed. | 0 | ||
| Rees; Visual Consciousness | 56 | Neural competition during rivalry may have been resolved by later stages of visual processing. | 1 | ||
| Rees; Visual Consciousness | 56 | Activity in ventral visual cortex is correlated with contents of consciousness. | 0 | ||
| Rees; Visual Consciousness | 56 | Studies of ambiguous figures have provided evidence to suggest the involvement of areas of frontal and parietal cortex in visual awareness. | 0 | ||
| Rees; Visual Consciousness | 56 | Cortical regions whose activity reflects perceptual transitions include ventral extrastriate cortex, and also parietal and frontal regions previously implicated in the control of attention. | 0 | ||
| Rees; Visual Consciousness | 56 | Activity in frontal and parietal cortex is specifically associated with perceptual alternations during binocular rivalry. | 0 | ||
| Rees; Visual Consciousness | 56 | Parietal and frontal regions are active during perceptual transitions occurring while viewing a range of bistabile figures (such as the Necker cube and the Rubins face/vase). | 0 | ||
| Rees; Visual Consciousness | 57 | Hallucination is a sensory perception experienced in the absence of an external stimulus (as distinct from an illusion, which is a misperception of an external stimulus induced by context). | 1 | ||
| Rees; Visual Consciousness | 57 | In contrast to hallucinations, illusions are misrepresentations of external stimuli. | 0 | ||
| Tsuchiya & Koch; Consciousness and Attention | 66 | Four-Fold Classification of Percepts and Behaviors (table) | 9 | ||
| Tsuchiya & Koch; Consciousness and Attention | 68 | Attention without Consciousness | 2 | ||
| Tsuchiya & Koch; Consciousness and Attention | 68 | Consciousness in the Absence of Attention | 0 | ||
| Tsuchiya & Koch; Consciousness and Attention | 68 | We are always aware of some aspects of the world around us, such as its jist. | 0 | ||
| Tsuchiya & Koch; Consciousness and Attention | 68 | In the 30 ms necessary to apprehend the gist of a scene, top-down attention cannot play much of a role (because gist is a property associated with the entire image). | 0 | ||
| Tsuchiya & Koch; Consciousness and Attention | 69 | Processing without Top-Down Attention and Consciousness | 1 | ||
| Tsuchiya & Koch; Consciousness and Attention | 72 | A philosopher has argued for the existence of two different types of consciousness -- phenomenal (P) and access (A). | 3 | ||
| Tsuchiya & Koch; Consciousness and Attention | 72 | Phenomenal consciousness is the ephemeral feeling of seeing yellow, different from the feeling of seeing green. | 0 | ||
| Tsuchiya & Koch; Consciousness and Attention | 72 | Access consciousness includes the processes that access information and do something with it, such as a verbal or motor report or working memory. | 0 | ||
| Tsuchiya & Koch; Consciousness and Attention | 74 | Much action bypasses conscious perception and introspection. | 2 | ||
| Tsuchiya & Koch; Consciousness and Attention | 74 | Anyone who skis mountain trails, plays a piano, or drives an automobile home on 'automatic pilot,' knows that stereotyped sensory-motor skills -- dubbed zombie behaviors -- require rapid and sophisticated sensory processing. | 0 | ||
| Raichle; Intrinsic Brain Activity | 81 | Human brain is approximately 2% of the weight of the body and yet accounts for 20% of its energy consumption. | 7 | ||
| Raichle; Intrinsic Brain Activity | 85 | A prominent feature of fMRI is that the unaveraged signal is quite noisy, prompting researchers to average their data to increase the signal to noise ratio. | 4 | ||
| Tononi; Sleep and Dreaming | 89 | Consciousness nearly fades during deep sleep early in the night, and returns later in the form of dreams. | 4 | ||
| Tononi; Sleep and Dreaming | 89 | During sleep, the brain goes through an orderly progression of changes in neural activity, epitomized by the occurrence of slow oscillations and spindles. | 0 | ||
| Tononi; Sleep and Dreaming | 90 | Sleep Stages and Cycles | 1 | ||
| Tononi; Sleep and Dreaming | 91 | Sleep patterns change markedly across the lifespan. | 1 | ||
| Tononi; Sleep and Dreaming | 91 | All-night recording of five sleep cycles. (diagram) | 0 | ||
| Tononi; Sleep and Dreaming | 92 | Major brain areas involved in initiating and maintaining wakefulness (diagram) | 1 | ||
| Tononi; Sleep and Dreaming | 93 | Neural Correlates of Wakefulness and Sleep | 1 | ||
| Tononi; Sleep and Dreaming | 95 | Consciousness in Sleep | 2 | ||
| Tononi; Sleep and Dreaming | 96 | NREM Sleep | 1 | ||
| Tononi; Sleep and Dreaming | 96 | REM Sleep | 0 | ||
| Tononi; Sleep and Dreaming | 98 | Dreams -- Consciousness in the Absence of Sensory Inputs and Self-reflection. | 2 | ||
| Tononi; Sleep and Dreaming | 100 | Internal generation of a world-analog. | 2 | ||
| Tononi; Sleep and Dreaming | 100 | Ability to dream requires the ability to imagine. | 0 | ||
| Tononi; Sleep and Dreaming | 101 | Many dreams are characterized by high degree of emotional involvement, especially fear and anxiety. | 1 | ||
| Tononi; Sleep and Dreaming | 101 | REM sleep is associated with a marked activation of the limbic and paralimpic structures such as the amygdala, the anterior cingulate cortex, the insula, and the medial orbitofrontal cortex. | 0 | ||
| Tononi; Sleep and Dreaming | 101 | Neuropsychology of dreaming. | 0 | ||
| Tononi; Sleep and Dreaming | 103 | Daydreaming | 2 | ||
| Tononi; Sleep and Dreaming | 103 | Lucid Dreaming | 0 | ||
| Tononi; Sleep and Dreaming | 103 | Sleepwalking | 0 | ||
| Tononi; Sleep and Dreaming | 104 | REM Sleep Behavior Disorder | 1 | ||
| Tononi; Sleep and Dreaming | 105 | Narcolepsy and Cataplexy | 1 | ||
| Tononi; Sleep and Dreaming | 105 | Narcolepsy is characterized by daytime sleepiness (sleep attacks). | 0 | ||
| Tononi; Sleep and Dreaming | 105 | Cataplexy (muscle weakness attacks). | 0 | ||
| Bassetti; Sleepwalking | 109 | During sleepwalking, the eyes are open and staring, patients can speak and answer to questions, usually in an incomprehensible manner. | 4 | ||
| Bassetti; Sleepwalking | 109 | Sleepwalkers are difficult to awaken, and when awakened, they appear confused. They may return spontaneously to bed and lie down. | 0 | ||
| Bassetti; Sleepwalking | 109 | There is usually no recall of sleepwalking episodes. | 0 | ||
| Bassetti; Sleepwalking | 110 | Sleepwalking appears between the ages of 5 and 15 years, with a peak around 8 -- 12 years. | 1 | ||
| Bassetti; Sleepwalking | 110 | Childhood sleepwalking usually disappears around puberty. | 0 | ||
| Bassetti; Sleepwalking | 110 | Duration of sleepwalking ranges from 1 -- 3 to 7 -- 10 minutes, rarely longer. | 0 | ||
| Bassetti; Sleepwalking | 110 | Patients are typically difficult to be awakened during a sleepwalking episode. | 0 | ||
| Bassetti; Sleepwalking | 110 | Episodes of sleepwalking often end with the patient returning to bed. | 0 | ||
| Alkire; General Anasthesia | 118 | Consciousness is widely held to be a neurobiological property of the brain. | 8 | ||
| Alkire; General Anasthesia | 118 | Without a brain there is no consciousness. | 0 | ||
| Alkire; General Anasthesia | 118 | Anesthesiologists chemically induce a temporary reversible state of unconsciousness for surgery. | 0 | ||
| Alkire; General Anasthesia | 118 | Anesthesiologists manipulate levels of consciousness. | 0 | ||
| Alkire; General Anasthesia | 118 | On rare occasions, patients having general anasthesia for surgery will remain conscious and aware during their operation, while appearing to be completely anesthetized. | 0 | ||
| Alkire; General Anasthesia | 124 | Brain imaging studies provide no definitive answer as to where anesthetics first work to cause unconsciousness. | 6 | ||
| Alkire; General Anasthesia | 124 | Temporal dynamics are far too slow to clarify which region (i.e. thalamus or cortex) is affected first by anasthesia and thus could be considered the primary cause of anesthetic-induced unconsciousness. | 0 | ||
| Alkire; General Anasthesia | 124 | A number of empirical findings support the hypothesis that the main effect of anasthesia occurs in the cortex. | 0 | ||
| Alkire; General Anasthesia | 125 | Researchers studying Parkinson's patients found indications that anesthetics first 'turn off' the cortex well before 'turning off' the thalamus. | 1 | ||
| Alkire; General Anasthesia | 127 | The decrease in relative thalamic activity found in brain imaging studies of anasthesia occurs as a direct result of a decreased corticothalamic feedback to the thalamus. | 2 | ||
| Alkire; General Anasthesia | 127 | The process by which anesthetics suppress arousal and cause unconsciousness likely involves a complex network of interacting components of the brain's arousal systems, for which the thalamus is but one (perhaps central) component. | 0 | ||
| Alkire; General Anasthesia | 127 | The posterior cingulate and medial parietal cortical areas are of some interest as potential neural correlates of consciousness. | 0 | ||
| Alkire; General Anasthesia | 127 | A number of the anesthetic agents suppress activity in the posterior cingulate and medial parietal cortical areas. | 0 | ||
| Alkire; General Anasthesia | 127 | The posterior parietal regions have been noted to show a relative decrease in functioning during altered states of consciousness, such as during the persistent vegetative state and sleep. | 0 | ||
| Alkire; General Anasthesia | 127 | A functional disconnection of the posterior brain regions within frontal brain regions appears associated with the unconsciousness of the persistent vegetative state, and restoration of connectivity between these regions has been associated with return to consciousness. | 0 | ||
| Alkire; General Anasthesia | 127 | The posterior brain regions, especially the posterior cingulate area, are involved in memory retrieval. | 0 | ||
| Alkire; General Anasthesia | 127 | Some evidence links the activity of the posterior brain regions, especially the medial parietal lobes, to the first-person perspective of consciousness. | 0 | ||
| Alkire; General Anasthesia | 127 | Long-established link between neglect syndromes and parietal damage. | 0 | ||
| Alkire; General Anasthesia | 127 | Recent work has shown that the posterior cingulate and the medial posterior parietal areas seemed to be involved in the generation of the baseline functional state of the human brain. One interpretation of this baseline concept is that the brain regions are active as a reflection of a person's self-conscious state when the brain is not involved in any specific cognitive task. | 0 | ||
| Alkire; General Anasthesia | 131 | English chemist Sir Humphrey Davy experimented on himself on the day after Christmas in the year 1799 regarding the nature of a newly discovered gas nitrous oxide. | 4 | ||
| Young; Coma | 137 | Coma is a state of unarousable unconsciousness due to the disfunction of the brain's ascending reticular activating system (ARAS), which is responsible for arousal and the maintenance of wakefulness. | 6 | ||
| Young; Coma | 137 | Anatomically and physiologically, ARAS has a redundancy of pathways and neurotransmitters; this may explain why coma is usually transient (seldom lasting more than three weeks). | 0 | ||
| Young; Coma | 137 | Emergence from coma is succeeded by outcomes ranging from the vegetative state to complete recovery, depending on the severity of damage to the cerebral cortex, the thalamus or their integrated function. | 0 | ||
| Young; Coma | 138 | For practical purposes, coma includes failure of eye opening to stimulation, motor response no better than simple withdrawal type movements, and a verbal response no better than simple vocalization of non-word sounds. | 1 | ||
| Young; Coma | 139 | There are numerous encephalopathies due to oxygen and organ failure. | 1 | ||
| Young; Coma | 143 | Concussion is a transient loss of consciousness after a blow to the head. | 4 | ||
| Young; Coma | 143 | Concussion is often accompanied by an anterograde post-traumatic amnesia (the inability to lay down new memories for a variable period (minutes to days) after the injury) plus or minus a shorter period of retrograde amnesia that precedes the injury. | 0 | ||
| Young; Coma | 143 | In concussion, brains are often morphologically normal. Since structural lesions are not essential, concussion appears to be more a disturbance of function than of structure. | 0 | ||
| Young; Coma | 145 | Locked-in Syndrome | 2 | ||
| Young; Coma | 148 | Brain Death | 3 | ||
| Bernat; Brain Death | 151 | Brain death is the common colloquial term for the determination of human death by showing the irreversible cessation of the clinical functions of the brain. | 3 | ||
| Owen; Vegetative State | 163 | Vegetative State | 12 | ||
| Owen; Vegetative State | 164 | Patients in the vegetative state are awake, but are assumed to be entirely unaware of self and environment. | 1 | ||
| Giacino; Minimally Conscious State | 173 | Minimally Conscious State | 9 | ||
| Giacino; Minimally Conscious State | 173 | Clinicians specializing in the care of patients with severe brain injury are well acquainted with the clinical features of coma and vegetative state (VS). | 0 | ||
| Giacino; Minimally Conscious State | 173 | Coma and vegetative state are characterized by the complete absence of behavioral signs of self and environmental awareness. | 0 | ||
| Gosseries; Locked-in Syndrome | 191 | Locked-in Syndrome | 18 | ||
| Gosseries; Locked-in Syndrome | 191 | Patients in locked in syndrome (LIS) are selectively deefferented, i.e. have no means of producing speech, limb, or face movements. | 0 | ||
| Gosseries; Locked-in Syndrome | 191 | Usually the anatomy of the responsible lesion in the brainstem is such that locked-in patients are left with the capacity to use vertical eye movements and blinking to communicate their awareness. | 0 | ||
| Gosseries; Locked-in Syndrome | 191 | Classical LIS is characterized by total immobility except for vertical eye movements or blinking. | 0 | ||
| Gosseries; Locked-in Syndrome | 191 | Incomplete LIS permits remnants of voluntary motion. | 0 | ||
| Gosseries; Locked-in Syndrome | 191 | Total LIS results in complete immobility including all eye movements combined with preserved consciousness. | 0 | ||
| Gosseries; Locked-in Syndrome | 193 | Long-term survival in LIS is rare. | 2 | ||
| Pietrini; Consciousness and Dementia | 204 | Consciousness and Dementia | 11 | ||
| Pietrini; Consciousness and Dementia | 204 | Information integration theory of consciousness -- consciousness corresponds to the brain's ability to rapidly integrate information. | 0 | ||
| Pietrini; Consciousness and Dementia | 204 | The brain's ability to integrate information requires a well functioning thalamocortical system. | 0 | ||
| Pietrini; Consciousness and Dementia | 204 | Extensive legions of the thalamocortical system are usually associated with a global loss of consciousness, such as that seen in comatose patients. | 0 | ||
| Pietrini; Consciousness and Dementia | 204 | Patients who have undergone surgical section of the corpus callosum for therapeutic purposes leading to a splitting of the thalamocortical system, consciousness is split. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Neural activity that correlates with conscious experience appears to be widely distributed over the cortex, indicating that consciousness is based on optimal functioning of a distributed thalamocortical network rather than on the activity of a specific single cortical region. | 1 | ||
| Pietrini; Consciousness and Dementia | 205 | Lesions of selected cortical areas result in the impairment of specific submodalities of conscious experience, such as the perception of faces, but do not produce any alterations of global consciousness. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Alzheimer's disease is the most common form of dementing disorders of the elderly, affecting more than 5% of individuals aged 65 and older in almost one out of two individuals over at over 85 years of age. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Alzheimer's disease shows a progressive, multivariate and irreversible deterioration of cognitive abilities. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Disturbances of attention and memory typically the first clinical manifestations in patients with Alzheimer's disease. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Cognitive impairment is due to the development of neuropathological processes characterized by the presence of senile plaques, neurofibrillary tangles and loss of neurons and their synaptic projections. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Neuropathological lesions affect mostly the neocortical association areas of the parietal, temporal and frontal lobes and limbic regions and show a regional distribution that may vary among individual patients. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Typically, the neuropathological process starts in the medial temporal lobe structures, including the entorhinal cortex and hippocampal formation, and subsequently spreads to the neocortical association areas of the temporal, parietal and frontal lobes, leading to the disruption of various mental functions. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | PET studies to measure regional cerebral glucose metabolism and blood flow in patients with Alzheimer's disease examined at rest (eyes patched, ears plugged, no sensory stimulation) as well is during a variety of cognitive tasks. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Measures of both cerebral glucose metabolism and blood flow are reliable indices of neuronal synaptic activity, as they reflect the brain's metabolic need for glucose and oxygen in order to produce ATP. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | ATP in the central nervous system is mostly required for the maintenance and restoration of ionic gradients and cell membrane potentials due to electrical activity associated with action potentials and transmission of impulses from neuron to neuron. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Changes in synaptical activity lead to changes in the demand for ATP and, in turn, for glucose utilization and capillary blood flow. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Cerebral glucose metabolism is impaired in Alzheimer's disease. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Regional cerebral glucose metabolism measured at rest is significantly reduced in patients with Alzheimer's disease. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Alzheimer's disease regional cerebral glucose metabolism is reduced mostly in association neocortical areas, with a relative sparing of primary neocortical and subcortical regions and cerebellum, at least until the later stages of the disease. | 0 | ||
| Pietrini; Consciousness and Dementia | 205 | Metabolic abnormalities worsened with the progression of dementia. | 0 | ||
| Pietrini; Consciousness and Dementia | 206 | Cerebral metabolic alterations are heterogeneous. | 1 | ||
| Pietrini; Consciousness and Dementia | 206 | Patterns of cerebral metabolic alterations are related to patterns of cognitive impairment. | 0 | ||
| Pietrini; Consciousness and Dementia | 206 | Distinct cognitive and cerebral metabolic features characterize clinical subtypes of Alzheimer's disease. | 0 | ||
| Pietrini; Consciousness and Dementia | 207 | Regional functional connectivity is altered in Alzheimer's disease. | 1 | ||
| Pietrini; Consciousness and Dementia | 207 | The correlation coefficient between the regional cerebral metabolic rates for glucose provides a measure for the functional association between distinct brain regions. | 0 | ||
| Pietrini; Consciousness and Dementia | 207 | The pattern of interregional correlations reflects the integrated cerebral activity either at rest or doing a specific cognitive task. | 0 | ||
| Pietrini; Consciousness and Dementia | 207 | Brain Gets Lost in a Degenerative Dementia | 0 | ||
| Pietrini; Consciousness and Dementia | 207 | Patients with Alzheimer's disease or with another similar dementia syndrome become more and more unaware of the world and of themselves, until they eventually slide in a meaningless present with a fading past and no future. | 0 | ||
| Pietrini; Consciousness and Dementia | 207 | Lack of awareness for the disease, anosognosia, or loss of insight are used interchangeably to indicate a patient inability to properly recognize their clinical condition, as is frequently observed in patients with Alzheimer's disease of frontotemporal dementia. | 0 | ||
| Pietrini; Consciousness and Dementia | 214 | Awareness of what happens around us and of ourselves is rooted in the complexity of the functional and anatomical networks of the thalamocortical system that enables the brain to rapidly integrate information. | 7 | ||
| Blumenfeld; Epilepsy | 247 | Conscious information processing depends on synchronous network activity in the brain. The same network that evolved for the generation of normal consciousness can be exploited by abnormally intense synchronous discharges, leading to epileptic seizures. | 33 | ||
| Blumenfeld; Epilepsy | 248 | Epileptic seizures cause transient, dynamic deficits in consciousness that can range from mild impairment of attention to complete behavioral unresponsiveness. | 1 | ||
| Blumenfeld; Epilepsy | 248 | Epileptic seizures are usually classified as either partial, meaning that they involve local regions of the brain, or generalized, meaning that they involve widespread regions of the brain bilaterally. | 0 | ||
| Blumenfeld; Epilepsy | 248 | Impaired consciousness is seen in generalized seizure types, such as absence (petite mal), and tonic-clonic (grand mal) seizures as well is in partial seizure types, namely complex partial temporal lobe seizures. | 0 | ||
| Blumenfeld; Epilepsy | 248 | Despite the differences between absence, tonic-clonic, and complex partial seizures, they all share a common thread of impaired consciousness. | 0 | ||
| Blumenfeld; Epilepsy | 248 | The three seizure types cause changes in (1) the upper brain stem and medial thalamus; (2) the anterior and posterior cingulate, medial frontal cortex, and precuneus; (3) the lateral and orbitofrontal cortex, and lateral parietal cortex. | 0 | ||
| Blumenfeld; Epilepsy | 249 | Consciousness depends on a network of cortical and subcortical structures. | 1 | ||
| Blumenfeld; Epilepsy | 249 | Consciousness has long been separated into structures necessary for controlling the level of consciousness, and those involved in generating the content of consciousness. | 0 | ||
| Blumenfeld; Epilepsy | 249 | Here we define the 'consciousness system' as those structures necessary for maintaining: (1) the alert awake state, (2) attention, and (3) awareness of self and the environment. | 0 | ||
| Blumenfeld; Epilepsy | 249 | The consciousness system at a minimum includes regions of the frontal and parietal association cortex, cingulate gyrus, precuneus, thalamus (especially the medial, midline, and intralamina nuclei), and multiple activating systems located in the basal forebrain, hypothalamus, midbrain, and upper pons. | 0 | ||
| Blumenfeld; Epilepsy | 249 | For the consciousness system, some researches would also include the basal ganglia and cerebellum due to the possible roles in controlling attention. | 0 | ||
| Blumenfeld; Epilepsy | 249 | Much prior work has demonstrated the importance of the midline subcortical structures and association cortex in normal consciousness. | 0 | ||
| Blumenfeld; Epilepsy | 250 | In the absence seizures, awareness briefly vanishes. Typical absence seizures consist of staring and unresponsiveness, often accompanied by subtle eyelid fluttering or mild myoclonic jerks. Duration is usually less than 10 seconds. | 1 | ||
| Blumenfeld; Epilepsy | 250 | Absence seizures occur most commonly in childhood. | 0 | ||
| Blumenfeld; Epilepsy | 250 | Absence seizures can occur in susceptible individuals up to several hundred times per day. | 0 | ||
| Blumenfeld; Epilepsy | 253 | Complex Partial Seizures | 3 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 261 | Research over the past 45 years on split-brain patients have revealed unique specialized processes in each hemisphere, including some recently discovered specialized processes in the right hemisphere. | 8 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 261 | Split-brain patients' talking left hemisphere consistently denies any change in their conscious experience as a result of severing the corpus callosum. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 261 | The experience of split-brain patients is indicative of a conscious system that is comprised of thousands of specialized local circuits. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 261 | One of several qualities that make split-brain patients so astonishing is that they seem utterly unaware of their special status. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 261 | For split-brain patients, the loss of the ability to transfer information from the left hemisphere to the right hemisphere and vice versa seems to have no impact on their overall psychological state. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 261 | In split-brain patients, the left brain does not seem to miss the right brain, despite recent discoveries of several specialized properties in the right hemisphere. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Consciousness does not constitute a single generalized process can but is an emergent property that arises out of hundreds if not thousands of specialized systems (modules). | 1 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Brain's specialized modules consist of neural circuitry specialized to process-specific domains of information. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Specialized neural circuitry enable the processing and mental representation of a specific aspect of conscious experience, and these circuits are widely distributed throughout the brain. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Many of these specialized circuits may be directly connected to some of the other specialized circuits, but not to most of them. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Each specialized circuit competes for attention. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | From moment to moment, different modules or systems will win the competition for attention and serve as the neural system underlying that moment of conscious experience. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | This dynamic moment-to-moment cacophony of systems comprises our consciousness. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | It appears to us as if our consciousness flows easily and naturally from one moment to the next with a single, unified, and coherent narrative. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Our sense of a unified experience emerges out of a particular specialized system call the 'interpreter,' which coordinates and continually interprets and makes sense of our behaviors, emotions, and thoughts. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | The interpreter appears to be uniquely human and specialized to the left hemisphere. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | A peculiar phenomenon that has been observed in a variety of neurological patients to deny that anything is wrong with them despite the clearly observable effects of the brain injury. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Anosognosia -- the unawareness or denying the existence of a brain injury deficit. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Anosognosia observed in many neurological disorders is indicative of a conscious system that is bound by the inputs of thousands of specialized local modules. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Left hemisphere specialization that is referred to as the 'interpreter' that unifies and interprets our conscious experience. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | A well-known example of anosognosia is often found in hemispatial neglect patients. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Anosognosia from hemispatial neglect is usually caused by a stroke to the right parietal lobe that causes disruption of attention and spatial awareness of the left side of space. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Damage to most areas of the nervous system that result in the impairment or loss of function will be noticed immediately by patients. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | Neglect patients, with damage to the right parietal lobe that also result in hemiplegia (paralysis to the left side of the body), deny their paralysis because these patients no longer have the mental representations of the existence of the left side of their body. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 262 | For neglect patients, with hemiplegia (paralysis to the left side of the body), there is no system to sense that something is wrong, so the patient assumes that everything is normal. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 263 | Reconcile current awareness with a memory of the pre-lesion awareness. A neglect patient may draw a picture of their home, but the picture they draw will only include the right side of their house. | 1 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 263 | For neglect patients, the visual information that was originally encoded in the brain is still available, but that information is neglected when memory systems attempt to retrieve it. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 263 | There are possibly hundreds of specialized systems in the human brain, from basic systems of perceptual processing (like discriminating tones and perceiving faces) to more higher-order systems (like recognizing emotions, sympathizing with others, and detecting cheaters). | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 263 | Just as the voices in a head of a schizophrenic patient can seem to them as real as the perception of actual voices, many distortions caused by brain injury can become incorporated into our conscious experience and not seem out of place. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 263 | Damage that specifically affects specialized memory systems that code for the familiarity of places and locations may increase the familiarity for otherwise novel or relatively new locations. These patients form delusional beliefs. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | In split-brain patients, most functions remain intact after the right hemisphere is disconnected from the left, including verbal IQ and many problem solving skills. | 3 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | The Left Hemisphere Interpreter -- Unifying the Conscious Experience. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | According to Gazzaniga's model of consciousness, there maybe hundreds, if not thousands, of modules contributing to our conscious experience, each contributing specialized bits of information. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | Even though there may be thousands of modules contributing to our conscious experience, our phenomenological experience will naturally flow from moment to moment, depending on the demands of the environment, as one unified and coherent experience. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | Gazzaniga believes that this unified and coherent experience of consciousness is due to a specialized process in the left hemisphere that he refers to as the 'interpreter.' | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | The interpreter is a specialized system that makes sense of all of the information bombarding the brain, interpreting our responses -- cognitive or emotional to what we encounter in our environment, asking how one thing relates to another, making hypotheses, bringing order on of chaos, creating a running narrative of our actions, emotions, thoughts, and dreams. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | The interpreter is the glue that keeps our story unified and creates our sense of being into a coherent, rational agent. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | Gazzaniga and colleagues first demonstrated the left hemisphere's unique drive to interpret the world around it using the simultaneous concept tests on a split-brain patient. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 266 | The specialized system in the brain that is driven to interpret is adaptive on an evolutionary scale because it allows the individual to quickly adapt to a wide range of unexpected events in the environment. | 0 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 267 | A function of the interpreter extends to the realm of problem-solving. The ability to make interpretations is a great problem-solving tool and very advantageous. However, when the sequence of events is purely random, then the drive to look for patterns and to formulate a hypothesis about the events can be suboptimal. | 1 | ||
| Gazzaniga; Left Hemisphere/Right Hemisphere | 267 | We are driven to form hypotheses and to look for patterns even when it is not warranted. Randomness tends to be a very difficult concept for humans, and a particularly difficult phenomenon for the interpreter. | 0 | ||
| Naccache; Visual Consciousness | 271 | Several neuropsychological syndromes contain marked dissociations, which permit the identification of principles related to the neurophysiology of consciousness. | 4 | ||
| Naccache; Visual Consciousness | 271 | Visual phenomenal consciousness is the aspect of consciousness most frequently investigated in neuroscience. | 0 | ||
| Naccache; Visual Consciousness | 271 | Through the exploration of neuropsychological syndromes such as 'blindsight,' visual form agnosia, optic ataxia, visual hallucinations, neglect, and split-brain cognition, the author highlights five general principles and explains how their generality has been demonstrated in healthy subjects using conditions such as visual illusions of subliminal perception. | 0 | ||
| Naccache; Visual Consciousness | 271 | A scientific model of consciousness based on the concept of a 'global workspace.' | 0 | ||
| Naccache; Visual Consciousness | 272 | Scientific investigation of consciousness, a major ongoing effort. | 1 | ||
| Naccache; Visual Consciousness | 273 | Multiple representations of the visual world elaborated by different visual brain areas (from retina and lateral geniculate nuclei to ventral occipito-temporal and dorsal occipito-parietal pathways in addition to superior colliculus mediated visual pathways). | 1 | ||
| Naccache; Visual Consciousness | 273 | Influential publication of Crick and Koch who proposed, mainly on the basis of neuro-anatomical data, that neural activity in area V1 does not contribute to the content about phenomenal consciousness. | 0 | ||
| Postle; Hippocampus, Memory, and Consciousness | 326 | Hippocampus, Memory, and Consciousness | 53 | ||
| Postle; Hippocampus, Memory, and Consciousness | 332 | Semantic knowledge that is independent of the episodes in which the information was learned. | 6 | ||
| Butler & Zeman; Transient Amnesia | 339 | Transient Amnesia | 7 | ||
| Nichelli; Aphasia | 352 | Aphasia | 13 | ||
| Pietrini; Blindness | 360 | Blindness and Consciousness | 8 | ||
| Tononi & Laureys; Neurology of Consciousness | 375 | Neurology of Consciousness -- Overview | 15 | ||
| Tononi & Laureys; Neurology of Consciousness | 377 | There have been claims that consciousness only emerges with language, though it seems preposterous to suggest that infants and animals are unconscious automata. | 2 | ||
| Tononi & Laureys; Neurology of Consciousness | 378 | Consciousness and Attention | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 379 | Consciousness and Memory | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 380 | The brain employs multiple maps of external space, some unimodal, some multimodal, many in the cerebral cortex, especially but not exclusively in parietal lobes, but some also in thalamus and colliculi. | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 381 | Consciousness and Space -- Neglect | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 382 | Consciousness, Body, and Self | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 382 | The narrative, autobiographical self -- the one that characterizes in a fundamental sense who we are. | 0 | ||
| Tononi & Laureys; Neurology of Consciousness | 385 | Consciousness and Anosognosia | 3 | ||
| Tononi & Laureys; Neurology of Consciousness | 386 | Global Alterations of Consciousness | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 386 | Sleep | 0 | ||
| Tononi & Laureys; Neurology of Consciousness | 387 | Anasthesia | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 388 | Coma and Vegetative States | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 388 | Coma -- an enduring sleep-like state of immobility with eyes closed from which the patient cannot be aroused. | 0 | ||
| Tononi & Laureys; Neurology of Consciousness | 389 | Seizures | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 390 | Neuroanatomy of Consciousness | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 390 | The only conclusion that can be drawn for sure about the neural substrate of consciousness is that it includes parts of the corticothalamic system. | 0 | ||
| Tononi & Laureys; Neurology of Consciousness | 391 | The reticular activating system appears to have the role of an on-off switch rather than a generator of consciousness. | 1 | ||
| Tononi & Laureys; Neurology of Consciousness | 391 | Even widespread cerebellar lesions or oblations hardly affect consciousness, yet this cerebellum has even more neurons than the cerebral cortex, and is strongly connected in both directions with thalamus and cortex, and often shows selective activation during cognitive tasks and in relation to emotion. | 0 | ||
| Tononi & Laureys; Neurology of Consciousness | 391 | The thalamus is sometimes considered as a seventh layer of cortex. | 0 | ||