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  1. Spanning the levels in cerebellar function.Michael A. Arbib - 1996 - Behavioral and Brain Sciences 19 (3):434-435.
    We ask what cerebellum and basal ganglia arguing that cerebellum tunes motor schemas and their coordination. We argue for a synthesis of models addressing the real-time role and error signaling roles of climbing fibers. bridges between regional and neuro-physiological studies, while relates the neurochemis-try of learning to neural and behavioral levels. [CRÉPEL et al.; HOUK et al.; KANO; LINDEN; SIMPSON et al.; SMITH; THACH; VINCENT].
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  • Is learning during anaesthesia implicit?Jackie Andrade - 1994 - Behavioral and Brain Sciences 17 (3):395-396.
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  • Is Eichenbaum et al.'s proposal testable and how extensive is the hippocampal memory system?John P. Aggleton - 1994 - Behavioral and Brain Sciences 17 (3):472-473.
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  • Personality and Authenticity in Light of the Memory-Modifying Potential of Optogenetics: A Reply to Objections about Potential Therapeutic Applicability of Optogenetics.Agnieszka K. Adamczyk & Przemysław Zawadzki - 2021 - American Journal of Bioethics Neuroscience 15 (2):W4-W7.
    There has been a growing interest in research concerning memory modification technologies (MMTs) in recent years. Neuroscientists and psychologists are beginning to explore the prospect of controllable and intentional modification of human memory. One of the technologies with the greatest potential to this end is optogenetics—an invasive neuromodulation technique involving the use of light to control the activity of individual brain cells. It has recently shown the potential to modify specific long-term memories in animal models in ways not yet possible (...)
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  • Empirical evidence and the knowledge-that/knowledge-how distinction.Marcus P. Adams - 2009 - Synthese 170 (1):97-114.
    In this article I have two primary goals. First, I present two recent views on the distinction between knowledge-that and knowledge-how (Stanley and Williamson, The Journal of Philosophy 98(8):411–444, 2001; Hetherington, Epistemology futures, 2006). I contend that neither of these provides conclusive arguments against the distinction. Second, I discuss studies from neuroscience and experimental psychology that relate to this distinction. Having examined these studies, I then defend a third view that explains certain relevant data from these studies by positing the (...)
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  • Modularity need not imply locality: Damaged modules can have nonlocal effects.Edgar Zurif & David Swinney - 1994 - Behavioral and Brain Sciences 17 (1):89-90.
  • Functional distinctions within the medical temporal lobe memory system: What is the evidence?Stuart Zola-Morgan & Pablo Alvarez - 1994 - Behavioral and Brain Sciences 17 (3):495-496.
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  • Emotion Regulation of Hippocampus Using Real-Time fMRI Neurofeedback in Healthy Human.Yashuo Zhu, Hui Gao, Li Tong, ZhongLin Li, Linyuan Wang, Chi Zhang, Qiang Yang & Bin Yan - 2019 - Frontiers in Human Neuroscience 13.
  • Personality and Authenticity in Light of the Memory-Modifying Potential of Optogenetics.Przemysław Zawadzki & Agnieszka K. Adamczyk - 2021 - American Journal of Bioethics Neuroscience 12 (1):3-21.
    There has been a growing interest in research concerning memory modification technologies (MMTs) in recent years. Neuroscientists and psychologists are beginning to explore the prospect of controllable and intentional modification of human memory. One of the technologies with the greatest potential to this end is optogenetics—an invasive neuromodulation technique involving the use of light to control the activity of individual brain cells. It has recently shown the potential to modify specific long-term memories in animal models in ways not yet possible (...)
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  • What counts as local?Andrew W. Young - 1994 - Behavioral and Brain Sciences 17 (1):88-89.
  • Non-spatial similarity can bias spatial distances in a cognitive map.Xing Xing & Jeffrey A. Saunders - 2022 - Cognition 229 (C):105251.
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  • On Common Ground: Jost's (1897) Law of Forgetting and Ribot's (1881) Law of Retrograde Amnesia.John T. Wixted - 2004 - Psychological Review 111 (4):864-879.
  • Subconscious detection of threat as reflected by an enhanced response bias.Sabine Windmann & Thomas Krüger - 1998 - Consciousness and Cognition 7 (4):603-633.
    Neurobiological and cognitive models of unconscious information processing suggest that subconscious threat detection can lead to cognitive misinterpretations and false alarms, while conscious processing is assumed to be perceptually and conceptually accurate and unambiguous. Furthermore, clinical theories suggest that pathological anxiety results from a crude preattentive warning system predominating over more sophisticated and controlled modes of processing. We investigated the hypothesis that subconscious detection of threat in a cognitive task is reflected by enhanced ''false signal'' detection rather than by selectively (...)
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  • On the creation of classification systems of memory.Daniel B. Willingham - 1994 - Behavioral and Brain Sciences 17 (3):426-427.
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  • Hippocampal neuronal activity in rat and primate: Memory and movement.Frasar A. W. Wilson - 1994 - Behavioral and Brain Sciences 17 (3):499-500.
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  • Plasticity of cerebro-cerebellar interactions in patients with cerebellar dysfunction.Karl Wessel - 1996 - Behavioral and Brain Sciences 19 (3):481-482.
    Studies comparing movement-related cortical potentials, post-excitatory inhibition after transcranial magnetic brain stimulation, and PET findings in normal controls and patients with cerebellar degeneration demonstrate plasticity of cerebro-cerebellar interactions and hereby support Thach's theory that the cerebellum has the ability to play a role in building behavioral context-response linkages and to build up appropriate responses from simpler constitutive elements, [THACH].
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  • Eyeblink conditioning, motor control, and the analysis of limbic-cerebellar interactions.Craig Weiss & John F. Disterhoft - 1996 - Behavioral and Brain Sciences 19 (3):479-481.
    Several target articles in this BBS special issue address the topic of cerebellar and olivary functions, especially as they pertain to motor earning. Another important topic is the neural interaction between the limbic system and the cerebellum during associative learning. In this commentary we present some of our data on olivo-cerebellar and limbic-cerebellar interactions during eyeblink conditioning. [HOUK et al.; SIMPSON et al.; THACH].
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  • The localization/distribution distinction in neuropsychology is related to the isomorphism/multiple meaning distinction in cell electrophysiology.Gerald S. Wasserman - 1994 - Behavioral and Brain Sciences 17 (1):87-88.
  • Reconsidering unconscious persistence: Suppressing unwanted memories reduces their indirect expression in later thoughts.Yingying Wang, Andrea Luppi, Jonathan Fawcett & Michael C. Anderson - 2019 - Cognition 187 (C):78-94.
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  • No more news from the cerebellum.Steven R. Vincent - 1996 - Behavioral and Brain Sciences 19 (3):490-492.
  • What behavioral benefit does stiffness control have? An elaboration of Smith's proposal.Gerard P. Van Galen, Angelique W. Hendriks & Willem P. DeJong - 1996 - Behavioral and Brain Sciences 19 (3):478-479.
  • The symbolic brain or the invisible hand?René van Hezewijk & Edward H. F. de Haan - 1994 - Behavioral and Brain Sciences 17 (1):85-86.
  • Sensorimotor learning in structures “upstream” from the cerebellum.Paul van Donkelaar - 1996 - Behavioral and Brain Sciences 19 (3):477-478.
  • Playing Flourens to Fodor's Gall.Tim van Gelder - 1994 - Behavioral and Brain Sciences 17 (1):84-84.
  • Prosopagnosia, conscious awareness and the interactive brain.Robert Van Gulick - 1994 - Behavioral and Brain Sciences 17 (1):84-85.
  • The functional architecture of visual attention may still be modular.Carlo Umiltà - 1994 - Behavioral and Brain Sciences 17 (1):82-83.
  • The Influences of Emotion on Learning and Memory.Chai M. Tyng, Hafeez U. Amin, Mohamad N. M. Saad & Aamir S. Malik - 2017 - Frontiers in Psychology 8:235933.
    Emotion has a substantial influence on the cognitive processes in humans, including perception, attention, learning, memory, reasoning, and problem solving. Emotion has a particularly strong influence on attention, especially modulating the selectivity of attention as well as motivating action and behavior. This attentional and executive control is intimately linked to learning processes, as intrinsically limited attentional capacities are better focused on relevant information. Emotion also facilitates encoding and helps retrieval of information efficiently. However, the effects of emotion on learning and (...)
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  • What do animal models of memory model?Endel Tulving & Hans J. Markowitsch - 1994 - Behavioral and Brain Sciences 17 (3):498-499.
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  • Computation, PET images, and attention.John K. Tsotsos - 1995 - Behavioral and Brain Sciences 18 (2):372-372.
    Posner & Raichle (1994) is a nice addition to the Scientific American Library and the average reader will both enjoy the book and learn a great deal. As an activeresearcher, however, I find the book disappointing in many respects. My two major disappointments are in the illusion of computation that is created throughout the volume and in the inadequate perspective of the presentation on visual attention.
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  • Limitations of PET and lesion studies in defining the role of the human cerebellum in motor learning.D. Timmann & H. C. Diener - 1996 - Behavioral and Brain Sciences 19 (3):477-477.
    PET studies using classical conditioning paradigms are reported. It is emphasized that PET studies show and not in learning paradigms. The importance of dissociating motor performance and learning deficits in human lesions studies is demonstrated in two exemplary studies. The different role of the cerebellum in adaptation of postural reflexes and learning of complex voluntary arm movements is discussed, [THACH].
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  • Motor learning and synaptic plasticity in the cerebellum.Richard F. Thompson - 1996 - Behavioral and Brain Sciences 19 (3):475-477.
    For reasons I have never understood, some students of the cerebellum have been unwilling to accept the now overwhelming evidence that the cerebellum exhibits lasting synaptic plasticity and plays an essential role in some forms of learning and memory. With a few exceptions (e.g., target article by SIMPSON et al.) this is no longer the case, as is clear in the excellent target articles on cerebellar LTD and the excellent target review by HOUK et al. [CRÉPEL et al.; HOUR et (...)
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  • Emotional arousal enhances word repetition priming.Laura Thomas & Kevin LaBar - 2005 - Cognition and Emotion 19 (7):1027-1047.
  • Q: Is the cerebellum an adaptive combiner of motor and mental/motor activities? A: Yes, maybe, certainly not, who can say?W. Thomas Thach - 1996 - Behavioral and Brain Sciences 19 (3):501-528.
  • How crosstalk creates vision-related eureka moments.George Terzis - 2001 - Philosophical Psychology 14 (4):393 – 421.
    The discussion begins with a familiar and defensible characterization of the eureka moment, according to which it is the unexpected product of separate and often seemingly incompatible perspectives. The principal aim of the discussion is to explain how, so characterized, vision-related eureka moments can occur. To fulfill this aim, the discussion employs a notion of crosstalk, in which cognitive interference slightly increases as a result of the creative thinker's considerable, albeit only partly successful, pre-eureka cognitive effort. Such crosstalk, it is (...)
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  • Are infants human?H. S. Terrace - 1994 - Behavioral and Brain Sciences 17 (3):425-426.
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  • On the relationship between persistent delay activity, repetition enhancement and priming.Elisa M. Tartaglia, Gianluigi Mongillo & Nicolas Brunel - 2014 - Frontiers in Psychology 5.
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  • We know a lot about the cerebellum, but do we know what motor learning is?Stephan P. Swinnen, Charles B. Walter & Natalia Dounskaia - 1996 - Behavioral and Brain Sciences 19 (3):474-475.
    In the behavioral literature on human movement, a distinction is made between the learning of parameters and the learning of new movement forms or topologies. Whereas the target articles by Thach, Smith, and Houk et al. provide evidence for cerebellar involvement in parametrization learning and adaptation, the evidence in favor of its involvement in the generation of new movement patterns is less straightforward. A case is made for focusing more attention on the latter issue in the future. This would directly (...)
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  • Is awareness necessary for operant conditioning?Frode Svartdal - 1994 - Behavioral and Brain Sciences 17 (3):424-425.
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  • What can neuroanatomy tell us about the functional components of the hippocampal memory system?Wendy A. Suzuki - 1994 - Behavioral and Brain Sciences 17 (3):496-498.
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  • How to link the specificity of cerebellar anatomy to motor learning?Fahad Sultan, Detlef Heck & Harold Bekkering - 1996 - Behavioral and Brain Sciences 19 (3):474.
  • Mental time travel in animals?Thomas Suddendorf & Janie Busby - 2003 - Trends in Cognitive Sciences 7 (9):391-396.
    Are humans alone in their ability to reminisce about the past and imagine the future? Recent evidence suggests that food-storing birds (scrub jays) have access to information about what they have stored where and when. This has raised the possibility of mental time travel (MTT) in animals and sparked similar research with other species. Here we caution that such data do not provide convincing evidence for MTT. Examination of characteristics of human MTT (e.g. non-verbal declaration, generativity, developmental prerequisites) points to (...)
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  • Whither learning, whither memory?Michael A. Stadler & Peter A. Frensch - 1994 - Behavioral and Brain Sciences 17 (3):423-424.
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  • Conscious belief as constructed memory: an empirical challenge to dispositionalism.Vishnu Sridharan - 2015 - Mind and Society 14 (1):21-33.
    There is an emerging consensus that human behavior is governed by two types of processes: System 1 processes, which are quicker, automatic, and run in parallel, and System 2 processes, which are slower, more conscious, and run in serial. Among such “dual-process” theorists, however, there is disagreement about whether the premises we use in our conscious, S2 reasoning should be considered as beliefs. In this exchange, one facet that has been largely overlooked is how conscious beliefs are structurally and functionally (...)
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  • Dissociable learning and memory systems of the brain.Larry R. Squire, Stephan Hamann & Barbara Knowlton - 1994 - Behavioral and Brain Sciences 17 (3):422-423.
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  • Methods, minds, memory, and kinds.Alison Springle - 2019 - Philosophical Psychology 32 (5):635-661.
    ABSTRACTThe acquisition of a skill, or knowledge-how, on the one hand, and the acquisition of a piece of propositional knowledge on the other, appear to be different sorts of epistemic achievements. Does this difference lie in the nature of the knowledge involved, marking a joint between knowledge-how and propositional knowledge? Intellectualists say no: All knowledge is propositional knowledge. Anti-intellectualists say yes: Knowledge-how and propositional knowledge are different in kind. What resources or methods may we legitimately and fruitfully employ to adjudicate (...)
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  • Intelligent machines and human minds.Elizabeth S. Spelke & Joseph A. Blass - 2017 - Behavioral and Brain Sciences 40.
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  • What are the best strategies for understanding hippocampal function?Paul R. Solomon & Bo-Yi Yang - 1994 - Behavioral and Brain Sciences 17 (3):494-495.
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  • Images of mind: A window to the brain.Robert L. Solso - 1995 - Behavioral and Brain Sciences 18 (2):371-371.
    The authors ofImages of the Mindhave made a significant contribution to our understanding of the brain through imaging technology. The book is well written, timely, beautifully illustrated and conveys a sense of history. It will appeal to alay audience as well as a professional audience.
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  • Resilient cerebellar theory complies with stiff opposition.Allan M. Smith - 1996 - Behavioral and Brain Sciences 19 (3):499-501.
    In response to several requests from commentators, an unambiguous definition of time-varying joint stiffness is provided. However, since a variety of different operations can be used to measure stiffness, a problem for quantification admittedly still exists. Several commentaries pointed out the advantage of controlling joint stiffness in optimizing the speed-accuracy trade-off known as Fittss law. The deficit in rapid reciprocal movements and the impact on joint stiffness inhibition caused by cerebellar lesions is clarified here, as the target article was apparently (...)
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  • Alternative strategies of categorization.Edward E. Smith, Andrea L. Patalano & John Jonides - 1998 - Cognition 65 (2-3):167-196.