Results for 'cerebellar cortex'

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  1.  8
    Distribution of activity in the cerebellar cortex resulting from passive limb movement.R. E. Poppele & G. Bosco - 1997 - Behavioral and Brain Sciences 20 (2):262-263.
    The notion that cerebellar cortex geometry may play a unique role in its function is explored by Braitenberg et al. in the form of a new theory about the distribution of cortical activity. The theory makes specific predictions which are not verified by an experimental study of hindlimb movement in the cat.
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  2.  18
    David Marr: A theory of the cerebellar cortex.A. J. Pellionisz - 1986 - In G. Palm & A. Aertsen (eds.), Brain Theory. Springer. pp. 253--257.
  3.  40
    Cerebellar networks with the cerebral cortex and basal ganglia.Andreea C. Bostan, Richard P. Dum & Peter L. Strick - 2013 - Trends in Cognitive Sciences 17 (5):241-254.
  4.  10
    33 Basal Ganglia and Cerebellar Circuits with the Cerebral Cortex.Peter L. Strick - 2004 - In Michael S. Gazzaniga (ed.), The Cognitive Neurosciences Iii. MIT Press. pp. 453.
  5.  49
    The Effect of Repetitive Transcranial Magnetic Stimulation of Cerebellar Swallowing Cortex on Brain Neural Activities: A Resting-State fMRI Study.Linghui Dong, Wenshuai Ma, Qiang Wang, Xiaona Pan, Yuyang Wang, Chao Han & Pingping Meng - 2022 - Frontiers in Human Neuroscience 16.
    ObjectiveThe effects and possible mechanisms of cerebellar high-frequency repetitive transcranial magnetic stimulation on swallowing-related neural networks were studied using resting-state functional magnetic resonance imaging.MethodA total of 23 healthy volunteers were recruited, and 19 healthy volunteers were finally included for the statistical analysis. Before stimulation, the cerebellar hemisphere dominant for swallowing was determined by the single-pulse TMS. The cerebellar representation of the suprahyoid muscles of this hemisphere was selected as the target for stimulation with 10 Hz rTMS, 100% (...)
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  6.  23
    Cerebellar purkinje units – basic functional elements of movement control.Gilbert A. Chauvet - 1997 - Behavioral and Brain Sciences 20 (2):247-248.
    Braitenberg et al.'s target article presents the best current integration of anatomical and physiological data, and provides a qualitative description of cerebellar function in terms of the dynamics of processes based on the geometry of the cerebellar cortex. We compare the proposed model to our own quantitative model based on the concept of Purkinjeunit.
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  7.  6
    Branching of cerebellar parallel fibres can assist the convergence of mossy fibre input sequences that are temporally and spatially dispersed.M. Lidierth - 1997 - Behavioral and Brain Sciences 20 (2):254-254.
    It is suggested that bifurcation of parallel fibres in the cerebellar cortex assists the spatiotemporal convergence of temporally dispersed and asomatotopic inputs to granule cells. This increases the number of combinations of inputs which can be compared for the purpose of sequence recognition.
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  8.  12
    Microcomplexes: The basic unit of the cerebellar role in adaptive motor control.Michael A. Arbib & Jacob Spoelstra - 1997 - Behavioral and Brain Sciences 20 (2):245-246.
    We offer a critique of the role of the parallel fiber beam as the unit of cerebellar computation, with the as its mode of operation. Instead we see the microcomplex linking cerebellar cortex and nuclei as the unit, with parallel fibers providing the means to coordinate the effects of microcomplexes in modulating various motor pattern generators (MPGs).
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  9.  8
    Does anodal cerebellar tDCS boost transfer of after-effects from throwing to pointing during prism adaptation?Lisa Fleury, Francesco Panico, Alexandre Foncelle, Patrice Revol, Ludovic Delporte, Sophie Jacquin-Courtois, Christian Collet & Yves Rossetti - 2022 - Frontiers in Psychology 13.
    Prism Adaptation is a useful method to study the mechanisms of sensorimotor adaptation. After-effects following adaptation to the prismatic deviation constitute the probe that adaptive mechanisms occurred, and current evidence suggests an involvement of the cerebellum at this level. Whether after-effects are transferable to another task is of great interest both for understanding the nature of sensorimotor transformations and for clinical purposes. However, the processes of transfer and their underlying neural substrates remain poorly understood. Transfer from throwing to pointing is (...)
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  10. The detection and generation of sequences as a key to cerebellar function: Experiments and theory.Valentino Braitenberg, Detlef Heck & Fahad Sultan - 1997 - Behavioral and Brain Sciences 20 (2):229-245.
    Starting from macroscopic and microscopic facts of cerebellar histology, we propose a new functional interpretation that may elucidate the role of the cerebellum in movement control. The idea is that the cerebellum is a large collection of individual lines (Eccles's : Eccles et al. 1967a) that respond specifically to certain sequences of events in the input and in turn produce sequences of signals in the output. We believe that the sequence-in/sequence-out mode of operation is as typical for the (...) cortex as the transformation of sets into sets of active neurons is typical for the cerebral cortex, and that both the histological differences between the two and their reciprocal functional interactions become understandable in the light of this dichotomy. The response of Purkinje cells to sequences of stimuli in the mossy fiber system was shown experimentally by Heck on surviving slices of rat and guinea pig cerebellum. Sequential activation of a row of eleven stimulating electrodes in the granular layer, imitating a of the stimuli along the folium, produces a powerful volley in the parallel fibers that strongly excites Purkinje cells, as evidenced by intracellular recording. The volley, or has maximal amplitude when the stimulus moves toward the recording site at the speed of conduction in parallel fibers, and much smaller amplitudes for lower or higher The succession of stimuli has no effect when they in the opposite direction. Synchronous activation of the stimulus electrodes also had hardly any effect. We believe that the sequences of mossy fiber activation that normally produce this effect in the intact cerebellum are a combination of motor planning relayed to the cerebellum by the cerebral cortex, and information about ongoing movement, reaching the cerebellum from the spinal cord. The output elicited by the specific sequence to which a is tuned may well be a succession of well timed inhibitory volleys the motor sequences so as to adapt them to the complicated requirements of the physics of a multijointed system. (shrink)
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  11. The Evolution of Language: The Cerebro-Cerebellar Blending of Visual-Spatial Working Memory with Vocalizations.Larry Vandervert - 2011 - Journal of Mind and Behavior 32 (4):317.
    Leiner, Leiner, and Dow proposed that the co-evolution of cerebral cortex and the cerebellum over the last million years gave rise to the unique cognitive capacities and language of humans. Following the findings of recent imaging studies by Imamizu and his colleagues, it is proposed that over the last million or so years language evolved from the blending of decomposed/re-composed contexts or "moments" of visual-spatial experience with those of sound patterns decomposed/re-composed from parallel context-appropriate vocalizations . It is further (...)
     
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  12. Reconfiguration of Functional Dynamics in Cortico-Thalamo-Cerebellar Circuit in Schizophrenia Following High-Frequency Repeated Transcranial Magnetic Stimulation.Huan Huang, Bei Zhang, Li Mi, Meiqing Liu, Xin Chang, Yuling Luo, Cheng Li, Hui He, Jingyu Zhou, Ruikun Yang, Hechun Li, Sisi Jiang, Dezhong Yao, Qifu Li, Mingjun Duan & Cheng Luo - 2022 - Frontiers in Human Neuroscience 16.
    Schizophrenia is a serious mental illness characterized by a disconnection between brain regions. Transcranial magnetic stimulation is a non-invasive brain intervention technique that can be used as a new and safe treatment option for patients with schizophrenia with drug-refractory symptoms, such as negative symptoms and cognitive impairment. However, the therapeutic effects of transcranial magnetic stimulation remain unclear and would be investigated using non-invasive tools, such as functional connectivity. A longitudinal design was adopted to investigate the alteration in FC dynamics using (...)
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  13.  17
    Specific sensorimotor interneuron circuits are sensitive to cerebellar-attention interactions.Jasmine L. Mirdamadi & Sean K. Meehan - 2022 - Frontiers in Human Neuroscience 16.
    Background: Short latency afferent inhibition provides a method to investigate mechanisms of sensorimotor integration. Cholinergic involvement in the SAI phenomena suggests that SAI may provide a marker of cognitive influence over implicit sensorimotor processes. Consistent with this hypothesis, we previously demonstrated that visual attention load suppresses SAI circuits preferentially recruited by anterior-to-posterior -, but not posterior-to-anterior -current induced by transcranial magnetic stimulation. However, cerebellar modulation can also modulate these same AP-sensitive SAI circuits. Yet, the consequences of concurrent cognitive and (...)
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  14.  28
    The cerebellum and cerebral cortex: Contrasting and converging contributions to spatial navigation and memory.Shane M. O'Mara - 1996 - Behavioral and Brain Sciences 19 (3):469-470.
    Thach's target article presents a remarkable overview and integration of animal and human studies on the functions of the cerebellum and makes clear theoretical predictions for both the normal operation of the cerebellum and for the effects of cerebellar lesions in the mature human. Commentary is provided on three areas, namely, spatial navigation, implicit learning, and cerebellar agenesis to elicit further development of the themes already present in Thach's paper, [THACH].
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  15.  31
    Origin of error signals during cerebellar learning of motor sequences.Michel Dufossé, Arthur Kaladjian & Philippe Grandguillaume - 1997 - Behavioral and Brain Sciences 20 (2):249-250.
    Prefrontal cerebral areas project to Purkinje cells, located in the most lateral part of the cerebellum, via mossy and climbing fibers. The latter olivary error signals reflect the attentional load of the prefrontal cortex. At the cerebral level, LTP-LTD plasticity allows these Purkinje cells to adaptively reinforce the active pyramidal cells involved in the motor sequence.
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  16.  7
    Nitric oxide and synaptic plasticity: NO news from the cerebellum.Steven R. Vincent - 1996 - Behavioral and Brain Sciences 19 (3):362-367.
    Interest in the role of nitric oxide (NO) in the nervous system began with the demonstration that glutamate receptor activation in cerebellar slices causes the formation of a diffusible messenger with properties similar to those of the endothelium-derived relaxing factor. It is now clear that this is due to the Ca2+/calmodulin-dependent activation of the enzyme NO synthase, which forms NO and citrulline from the amino acid L-arginine. The cerebellum has very high levels of NO synthase, and although it has (...)
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  17. Richard A. Andersen David zipser.Parietal Cortex - 1990 - In J. McGaugh, Jerry Weinberger & G. Lynch (eds.), Brain Organization and Memory. Guilford Press. pp. 271.
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  18.  14
    The Structured Event Complex and the Human.Prefrontal Cortex - 2002 - In Donald T. Stuss & Robert T. Knight (eds.), Principles of Frontal Lobe Function. Oxford University Press. pp. 292.
  19. Plasticity mechanisms of genetically distinct Purkinje cells.Stijn Voerman, Robin Broersen, Sigrid M. A. Swagemakers, Chris I. De Zeeuw & Peter J. van der Spek - forthcoming - Bioessays:2400008.
    Despite its uniform appearance, the cerebellar cortex is highly heterogeneous in terms of structure, genetics and physiology. Purkinje cells (PCs), the principal and sole output neurons of the cerebellar cortex, can be categorized into multiple populations that differentially express molecular markers and display distinctive physiological features. Such features include action potential rate, but also their propensity for synaptic and intrinsic plasticity. However, the precise molecular and genetic factors that correlate with the differential physiological properties of PCs (...)
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  20.  32
    Models of the cerebellum and motor learning.James C. Houk, Jay T. Buckingham & Andrew G. Barto - 1996 - Behavioral and Brain Sciences 19 (3):368-383.
    This article reviews models of the cerebellum and motor learning, from the landmark papers by Marr and Albus through those of the present time. The unique architecture of the cerebellar cortex is ideally suited for pattern recognition, but how is pattern recognition incorporated into motor control and learning systems? The present analysis begins with a discussion of exactly what the cerebellar cortex needs to regulate through its anatomically defined projections to premotor networks. Next, we examine various (...)
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  21.  42
    Information processing in neural networks by means of controlled dynamic regimes.François Chapeau-Blondeau - 1995 - Acta Biotheoretica 43 (1-2):155-167.
    This paper is concerned with the modeling of neural systems regarded as information processing entities. I investigate the various dynamic regimes that are accessible in neural networks considered as nonlinear adaptive dynamic systems. The possibilities of obtaining steady, oscillatory or chaotic regimes are illustrated with different neural network models. Some aspects of the dependence of the dynamic regimes upon the synaptic couplings are examined. I emphasize the role that the various regimes may play to support information processing abilities. I present (...)
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  22.  20
    Is the cerebellum essentially a precise pattern matching device?Franz Mechsner & Günther Palm - 1997 - Behavioral and Brain Sciences 20 (2):257-257.
    (1) The is not the only interpretation of cerebellar histology worth considering. Therefore, it is not imperative to strive for a theory of cerebellar function which gives it a prominent rôle. (2) The experiments with cannot support the tidal wave theory. (3) The notion that only can excite the cerebellar cortex is burdened with many intrinsic difficulties. (4) The common theoretical claim that the accuracy of skilled movements is due to exact pattern-matching processes in the cerebellum (...)
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  23.  36
    Sequences of sensory predictions.R. C. Miall - 1997 - Behavioral and Brain Sciences 20 (2):258-259.
    I argue that the rôle for the cerebellar cortex is in the generation of sensory predictions, not motor sequences. This proposal may explain the allometric relationship described in Braitenberg et al.'s target article. I also point out that the parallel beam organisation may have a nontemporal basis.
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  24.  17
    Spatio-temporal constraints of the tidal wave theory.Cornelius Schwarz - 1997 - Behavioral and Brain Sciences 20 (2):264-265.
    The tidal-wave theory is inspired by the particular morphology of the cerebellar cortex. It elegantly attributes function to the anisotropy of the cerebellar wiring and the geometry of Purkinje cell dendrites. In this commentary, physiological considerations are used to elaborate temporal and spatial constraints of the tidal-wave theory. It is shown, first, that limitations of temporal precision in the cortical inputs to the mammalian cerebellum delimit the spatial resolution of an input sequence (i.e., the minimal distance along (...)
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  25.  6
    Neural Correlates of Knee Extension and Flexion Force Control: A Kinetically-Instrumented Neuroimaging Study.Dustin R. Grooms, Cody R. Criss, Janet E. Simon, Adam L. Haggerty & Timothy R. Wohl - 2021 - Frontiers in Human Neuroscience 14.
    Background: The regulation of muscle force is a vital aspect of sensorimotor control, requiring intricate neural processes. While neural activity associated with upper extremity force control has been documented, extrapolation to lower extremity force control is limited. Knowledge of how the brain regulates force control for knee extension and flexion may provide insights as to how pathology or intervention impacts central control of movement.Objectives: To develop and implement a neuroimaging-compatible force control paradigm for knee extension and flexion.Methods: A magnetic resonance (...)
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  26.  32
    On the specific role of the cerebellum in motor learning and cognition: Clues from PET activation and lesion studies in man.W. T. Thach - 1996 - Behavioral and Brain Sciences 19 (3):411-433.
    Brindley proposed that we initially generate movements , under higher cerebral control. As the movement is practiced, the cerebellum learns to link within itself the context in which the movement is made to the lower level movement generators. Marr and Albus proposed that the linkage is established by a special input from the inferior olive, which plays upon an input-output element within the cerebellum during the period of the learning. When the linkage is complete, the occurrence of the context (represented (...)
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  27.  8
    Effective connectivity underlying neural and behavioral components of prism adaptation.Selene Schintu, Stephen J. Gotts, Michael Freedberg, Sarah Shomstein & Eric M. Wassermann - 2022 - Frontiers in Psychology 13.
    Prism adaptation is a form of visuomotor training that produces both sensorimotor and cognitive aftereffects depending on the direction of the visual displacement. Recently, a neural framework explaining both types of PA-induced aftereffects has been proposed, but direct evidence for it is lacking. We employed Structural Equation Modeling, a form of effective connectivity analysis, to establish directionality among connected nodes of the brain network thought to subserve PA. The findings reveal two distinct network branches: a loop involving connections from the (...)
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  28.  7
    Altered intrinsic brain activity and connectivity in unaffected parents of individuals with autism spectrum disorder: a resting-state fMRI study.Xiang-Wen Zhu, Li-Li Zhang, Zong-Ming Zhu, Luo-Yu Wang, Zhong-Xiang Ding & Xiang-Ming Fang - 2022 - Frontiers in Human Neuroscience 16:997150.
    Objectives: Autism spectrum disorder (ASD) is a juvenile onset neurodevelopmental disorder with social impairment and stereotyped behavior as the main symptoms. Unaffected relatives may also exhibit similar ASD features due to genetic factors. Although previous studies have demonstrated atypical brain morphological features as well as task-state brain function abnormalities in unaffected parents with ASD children, it remains unclear the pattern of brain function in the resting state.Methods: A total of 42 unaffected parents of ASD children (pASD) and 39 age-, sex-, (...)
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  29.  8
    Repetitive Transcranial Magnetic Stimulation Induces Quantified Functional and Structural Changes in Subcortical Stroke: A Combined Arterial Spin Labeling Perfusion and Diffusion Tensor Imaging Study.Yu Jin, Xi Bai, Binghu Jiang, Zhiwei Guo & Qiwen Mu - 2022 - Frontiers in Human Neuroscience 16.
    PurposeTo explore the changes of cerebral blood flow and fractional anisotropy in stroke patients with motor dysfunction after repetitive transcranial magnetic stimulation treatment, and to better understand the role of rTMS on motor rehabilitation of subcortical stroke patients from the perfusion and structural level.Materials and MethodsIn total, 23 first-episode acute ischemic stroke patients and sixteen healthy controls were included. The patients were divided into the rTMS and sham group. The rehabilitation assessments and examination of perfusion and structural MRI were performed (...)
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  30.  17
    The cognitive neuropsychology of the cerebellum.Timothy Justus & Richard Ivry - 2001 - International Review of Psychiatry 13 (4):276–282.
    We review evidence from neuropsychological studies of patients with damage to the cerebellum that suggests cerebellar involvement in four general categories of cognition: (1) speech and language; (2) temporal processing; (3) implicit learning and memory; (4) visuospatial processing and attention. A relatively strong case can be made for cerebellar contributions to language (including speech perception, lexical retrieval, and working memory) and to temporal processing. However, the evidence concerning cerebellar involvement in non-motor implicit learning and visuospatial processing is (...)
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  31.  11
    Which cerebellar cells contribute to extracellular cGMP?Lech Kiedrowski - 1996 - Behavioral and Brain Sciences 19 (3):464-465.
    Vincent proposes that the extracellular cGMP found in cerebellum after glutamate receptor activation is released mainly from Purkinje cells because in these neurons the presence of guanylate cyclase has been shown using monoclonal antibodies. It is uncertain, however, whether Purkinje cells are the only source of extracellular cGMP in the cerebellum. This commentary examines the possibility that glial and cerebellar granule cells may also participate in cGMP synthesis and release, Moreover, the hypothesis of transcellular metabolism of citrulline and arginine (...)
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  32.  52
    Cerebellar rhythms: Exploring another metaphor.Patrick D. Roberts, Gin McCollum & Jan E. Holly - 1996 - Behavioral and Brain Sciences 19 (3):471-472.
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  33.  52
    Motor cortex fields and speech movements: Simple dual control is implausible.James H. Abbs & Roxanne DePaul - 1998 - Behavioral and Brain Sciences 21 (4):511-512.
    We applaud the spirit of MacNeilage's attempts to better explain the evolution and cortical control of speech by drawing on the vast literature in nonhuman primate neurobiology. However, he oversimplifies motor cortical fields and their known individual functions to such an extent that he undermines the value of his effort. In particular, MacNeilage has lumped together the functional characteristics across multiple mesial and lateral motor cortex fields, inadvertantly creating two hypothetical centers that simply may not exist.
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  34.  5
    Cerebellar and brainstem differences in children with developmental coordination disorder: A voxel-based morphometry study.Kamaldeep K. Gill, Donna Lang & Jill G. Zwicker - 2022 - Frontiers in Human Neuroscience 16.
    Developmental coordination disorder is a neurodevelopmental disorder that significantly impairs a child’s ability to learn motor skills and to perform everyday activities. The cause of DCD is unknown; however, evidence suggests that children with DCD have altered brain structure and function. While the cerebellum has been hypothesised to be involved in developmental coordination disorder, no studies have specifically examined cerebellar structure in this population. The purpose of our study was to examine cerebellar differences in children with DCD compared (...)
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  35.  29
    Cerebellar involvement in movement timing on a variety of timescales.Jeffrey S. Grethe & Richard F. Thompson - 1997 - Behavioral and Brain Sciences 20 (2):250-251.
    The cerebellum has been hypothesized to play a role in a variety of movement timing tasks that involve the processing of temporal information on a variety of timescales. Braitenberg, Heck & Sultan propose a new theory of cerebellar function that is able to account for movement timing on the order of a couple of hundred milliseconds. However, this theory does not account for the rôle the cerebellum plays in the acquisition and retention of adaptively timed discrete movements that are (...)
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  36. Cerebellar Abnormalities on Proton MR Spectroscopy and Imaging in Patients With Gluten Ataxia: A Pilot Study.Vishwa Rawat, Ritu Tyagi, Inder Singh, Prasenjit Das, Achal Kumar Srivastava, Govind K. Makharia & Uma Sharma - 2022 - Frontiers in Human Neuroscience 16.
    Gluten ataxia is a rare immune-mediated neurological disorder caused by the ingestion of gluten. The diagnosis is not straightforward as antibodies are present in only up to 38% of patients, but often at lower titers. The symptoms of ataxia may be mild at the onset but lead to permanent damage if remain untreated. It is characterized by damage to the cerebellum however, the pathophysiology of the disease is not clearly understood. The present study investigated the neurochemical profile of vermis and (...)
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  37.  9
    Altered Cerebellar White Matter in Sensory Processing Dysfunction Is Associated With Impaired Multisensory Integration and Attention.Anisha Narayan, Mikaela A. Rowe, Eva M. Palacios, Jamie Wren-Jarvis, Ioanna Bourla, Molly Gerdes, Annie Brandes-Aitken, Shivani S. Desai, Elysa J. Marco & Pratik Mukherjee - 2021 - Frontiers in Psychology 11.
    Sensory processing dysfunction is characterized by a behaviorally observed difference in the response to sensory information from the environment. While the cerebellum is involved in normal sensory processing, it has not yet been examined in SPD. Diffusion tensor imaging scans of children with SPD and typically developing controls were compared for fractional anisotropy, mean diffusivity, radial diffusivity, and axial diffusivity across the following cerebellar tracts: the middle cerebellar peduncles, superior cerebellar peduncles, and cerebral peduncles. Compared to TDC, (...)
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  38.  13
    Cerebellar Functions.Andre Thomas - 1913 - Philosophical Review 22 (4):440.
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  39. Cerebral cortex as model builder.H. B. Barlow - 1985 - In David Rose & Vernon Dobson (eds.), Models of the Visual Cortex. New York: Wiley. pp. 37--46.
  40. Cerebellar syndromes.R. S. Dow - 1969 - In P. Vinken & G. Bruyn (eds.), Handbook of Clinical Neurology. North Holland. pp. 2--392.
     
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  41.  15
    Cerebellar theory out of control.Michael G. Paulin - 1996 - Behavioral and Brain Sciences 19 (3):470-471.
    The views of Houk et al., Smith, and Thach on the role of cerebellum in movement control differ substantially, but all three are flawed by the false reasoning that because information passes from the cerebellum to movements the cerebellum must be a movement controller, or a part of one. The divergent and less than compelling ideas expressed by these leading cerebellar theorists epitomize the fruitlessness of this paradigm, and signal the need for a change. [HOUK et al.; SMITH; THACH].
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  42.  13
    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 (...)
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  43.  31
    Cerebellar tDCS Does Not Enhance Performance in an Implicit Categorization Learning Task.Marie C. Verhage, Eric O. Avila, Maarten A. Frens, Opher Donchin & Jos N. van der Geest - 2017 - Frontiers in Psychology 8.
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  44.  10
    Cerebellar contributions to visuomotor adaptation and motor sequence learning: an ALE meta-analysis.Jessica A. Bernard & Rachael D. Seidler - 2013 - Frontiers in Human Neuroscience 7.
  45.  49
    Context, cortex, and dopamine: A connectionist approach to behavior and biology in schizophrenia.Jonathan D. Cohen & David Servan-Schreiber - 1992 - Psychological Review 99 (1):45-77.
  46.  21
    Decreased Cerebellar-Orbitofrontal Connectivity Correlates with Stuttering Severity: Whole-Brain Functional and Structural Connectivity Associations with Persistent Developmental Stuttering.Kevin R. Sitek, Shanqing Cai, Deryk S. Beal, Joseph S. Perkell, Frank H. Guenther & Satrajit S. Ghosh - 2016 - Frontiers in Human Neuroscience 10.
  47.  79
    Anomalous Cerebellar Anatomy in Chinese Children with Dyslexia.Ying-Hui Yang, Yang Yang, Bao-Guo Chen, Yi-Wei Zhang & Hong-Yan Bi - 2016 - Frontiers in Psychology 7.
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  48. Cerebellar atrophy of late onset.G. A. Jervis - 1969 - In P. Vinken & G. Bruyn (eds.), Handbook of Clinical Neurology. North Holland. pp. 42--135.
     
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  49.  9
    A cerebellar long-term depression update.David J. Linden - 1996 - Behavioral and Brain Sciences 19 (3):482-487.
  50.  7
    Cerebellar long-term depression as investigated in a cell culture preparation.David J. Linden - 1996 - Behavioral and Brain Sciences 19 (3):339-346.
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