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Dive into the research topics where Maria Felice Ghilardi is active.

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Featured researches published by Maria Felice Ghilardi.


Nature Neuroscience | 1999

Independent learning of internal models for kinematic and dynamic control of reaching.

John W. Krakauer; Maria Felice Ghilardi; Claude Ghez

Psychophysical studies of reaching movements suggest that hand kinematics are learned from errors in extent and direction in an extrinsic coordinate system, whereas dynamics are learned from proprioceptive errors in an intrinsic coordinate system. We examined consolidation and interference to determine if these two forms of learning were independent. Learning and consolidation of two novel transformations, a rotated spatial reference frame and altered intersegmental dynamics, did not interfere with each other and consolidated in parallel. Thus separate kinematic and dynamic models were constructed simultaneously based on errors computed in different coordinate frames, and possibly, in different sensory modalities, using separate working-memory systems. These results suggest that computational approaches to motor learning should include two separate performance errors rather than one.


Experimental Brain Research | 1994

Accuracy of planar reaching movements

James Gordon; Maria Felice Ghilardi; Scott E. Cooper; Claude Ghez

This study examined the variability in movement end points in a task in which human subjects reached to targets in different locations on a horizontal surface. The primary purpose was to determine whether patterns in the variable errors would reveal the nature and origin of the coordinate system in which the movements were planned. Six subjects moved a hand-held cursor on a digitizing tablet. Target and cursor positions were displayed on a computer screen, and vision of the hand and arm was blocked. The screen cursor was blanked during movement to prevent visual corrections. The paths of the movements were straight and thus directions were largely specified at the onset of movement. The velocity profiles were bell-shaped, and peak velocities and accelerations were scaled to target distance, implying that movement extent was also programmed in advance of the movement. The spatial distributions of movement end points were elliptical in shape. The major axes of these ellipses were systematically oriented in the direction of hand movement with respect to its initial position. This was true for both fast and slow movements, as well as for pointing movements involving rotations of the wrist joint. Using principal components analysis to compute the axes of these ellipses, we found that the eccentricity of the elliptical dispersions was uniformly greater for small than for large movements: variability along the axis of movement, representing extent variability, increased markedly but nonlinearly with distance. Variability perpendicular to the direction of movement, which results from directional errors, was generally smaller than extent variability, but it increased in proportion to the extent of the movement. Therefore, directional variability, in angular terms, was constant and independent of distance. Because the patterns of variability were similar for both slow and fast movements, as well as for movements involving different joints, we conclude that they result largely from errors in the planning process. We also argue that they cannot be simply explained as consequences of the inertial properties of the limb. Rather they provide evidence for an organizing mechanism that moves the limb along a straight path. We further conclude that reaching movements are planned in a hand-centered coordinate system, with direction and extent of hand movement as the planned parameters. Since the factors which influence directional variability are independent of those that influence extent errors, we propose that these two variables can be separately specified by the brain.


Experimental Brain Research | 1994

Accuracy of planar reaching movements - II. Systematic extent errors resulting from inertial anisotropy

James Gordon; Maria Felice Ghilardi; Scott E. Cooper; Claude Ghez

This study examines the source of directiondependent errors in movement extent made by human subjects in a reaching task. As in the preceding study, subjects were to move a cursor on a digitizing tablet to targets displayed on a computer monitor. Movements were made without concurrent visual feedback of cursor position, but movement paths were displayed on the monitor after the completion of each movement. We first examined horizontal hand movements made at waist level with the upper arm in a vertical orientation. Targets were located at five distances and two directions (30° and 150°) from one of two initial positions. Trajectory shapes were stereotyped, and movements to more distant targets had larger accelerations and velocities. Comparison of movements in the two directions showed that in the 30° direction responses were hypermetric, accelerations and velocities were larger, and movement times were shorter. Since movements in the 30° direction required less motion of the upper arm than movements in the 150° direction, we hypothesized that the differences in accuracy and acceleration reflected a failure to take into account the difference in total limb inertia in the two directions. To test this hypothesis we simulated the initial accelerations of a two-segment limb moving in the horizontal plane with the hand at shoulder level when a constant force was applied at the hand in each of 24 directions. We compared these simulated accelerations to ones produced by our subjects with their arms in the same position when they aimed movements to targets in the 24 directions and at equal distances from an initial position. The magnitudes of both simulated and actual accelerations were greatest in the two directions perpendicular to the forearm, where inertial resistance is least, and lowest for movements directed along the axis of the forearm. In all subjects, the directional variation in peak acceleration was similar to that predicted by the model and shifted in the same way when the initial position of the hand was displaced. The pattern of direction-dependent variations in initial acceleration did not depend on the speed of movement. It was also unchanged when subjects aimed their movements toward targets presented within the workspace on the tablet instead of on the computer monitor. These findings indicate that, in programming the magnitude of the initial force that will accelerate the hand, subjects do not fully compensate for direction-dependent differences in inertial resistance. The direction-dependent differences in peak acceleration were associated with systematic variations in movement extent in all subjects, but the variations in extent were proportionately smaller than those in acceleration. This compensation for inertial anisotropy, which differed in degree among subjects, was associated with changes in movement duration. The possible contributions of elastic properties of the musculoskeletal system and proprioceptive feed-back to the compensatory variations in movement time are discussed. The finding that the magnitude of the initial force that accelerates the hand is planned without regard to movement direction adds support for the hypothesis that extent and direction of an intended movement are planned independently. Furthermore, the lack of compensation for inertia in the acceleration of the simple reaching movements studied here suggests that they are planned by the central nervous system without explicit inverse kinematic and dynamic computations.


Annals of Neurology | 2001

Functional correlates of pallidal stimulation for Parkinson's disease

Masafumi Fukuda; Marc J. Mentis; Maria Felice Ghilardi; Vijay Dhawan; Angelo Antonini; John P. Hammerstad; Andres M. Lozano; Anthony E. Lang; Kelly Lyons; William C. Koller; Claude Ghez; David Eidelberg

We measured regional cerebral blood flow with H215O and positron emission tomography (PET) scanning at rest and during a motor task to study the mechanism of motor improvement induced by deep brain stimulation of the internal globus pallidus in Parkinsons disease. Six right‐handed patients with Parkinsons disease were scanned while performing a predictable paced sequence of reaching movements and while observing the same screen displays and tones. PET studies were performed ON and OFF stimulation in a medication‐free state. Internal globus pallidus deep brain stimulation improved off‐state United Parkinsons Disease Rating Scale motor ratings (37%, p < 0.002) and reduced timing errors (movement onset time, 55%, p < 0.01) as well as spatial errors (10%, p < 0.02). Concurrent regional cerebral blood flow recordings revealed a significant enhancement of motor activation responses in the left sensorimotor cortex (Brodmann area [BA] 4), bilaterally in the supplementary motor area (BA 6), and in the right anterior cingulate cortex (BA 24/32). Significant correlations were evident between the improvement in motor performance and the regional cerebral blood flow changes mediated by stimulation. With internal globus pallidus deep brain stimulation, improved movement initiation correlated with regional cerebral blood flow increases in the left sensorimotor cortex and ventrolateral thalamus and in the contralateral cerebellum. By contrast, improved spatial accuracy correlated with regional cerebral blood flow increases in both cerebellar hemispheres and in the left sensorimotor cortex. These results suggest that internal globus pallidus deep brain stimulation may selectively improve different aspects of motor performance. Multiple, overlapping neural pathways may be modulated by this intervention. Ann Neurol 2001:49:155–164


NeuroImage | 2004

Caudate nucleus: influence of dopaminergic input on sequence learning and brain activation in Parkinsonism

Maren Carbon; Yilong Ma; Anna Barnes; Vijay Dhawan; Thomas Chaly; Maria Felice Ghilardi; David Eidelberg

In this study, we tested the hypotheses that (1) the acquisition of sequential information is related to the integrity of dopaminergic input to the caudate nucleus; and (2) the integrity of dopaminergic input to the caudate nucleus correlates significantly with brain activation during sequence acquisition. Twelve early stage Parkinsons disease (PD) patients and six age-matched healthy volunteers were scanned using a dual tracer PET imaging design. All subjects were scanned with [(18)F]fluoropropyl-betaCIT (FPCIT) to measure striatal dopamine transporter (DAT) binding and with [(15)O]water to assess activation during a sequence learning task where movements were made to a repeating sequence of eight targets. Caudate and putamen DAT binding in the PD cohort was reduced by 15% and 43%, respectively. In PD, caudate DAT binding correlated with target acquisition (R = 0.57, P < 0.05), while putamen DAT binding did not correlate with performance. In volunteers, caudate DAT binding correlated with learning-related activation (P < 0.05, corrected for multiple comparisons) in the left dorsolateral and ventral prefrontal cortices, the anterior cingulate and premotor regions, and the right cerebellum. A significant correlation with caudate DAT binding was additionally detected in the right anteromedial thalamus, extending into the rostral midbrain. By contrast, in the PD cohort, most of these regional relationships were lost: Only ventral and dorsolateral prefrontal cortex activation correlated with caudate dopaminergic tone. Our findings suggest that sequence learning is normally associated with tight coupling between dopaminergic input to the caudate and thalamo-cortical functional activity. Despite minimal reductions in nigro-caudate input, PD patients demonstrate a loss of this coupling early in the disease.


Human Brain Mapping | 2003

Learning networks in health and Parkinson's disease: Reproducibility and treatment effects

Maren Carbon; Maria Felice Ghilardi; Andrew Feigin; Masafumi Fukuda; Giulia Silvestri; Marc J. Mentis; Claude Ghez; James R. Moeller; David Eidelberg

In a previous H215O/PET study of motor sequence learning, we used principal components analysis (PCA) of region of interest (ROI) data to identify performance‐related activation patterns in normal subjects and patients with Parkinsons disease (PD). In the present study, we determined whether these patterns predicted learning performance in subsequent normal and untreated PD cohorts. Using a voxel‐based PCA approach, we correlated the changes in network activity that occurred during antiparkinsonian treatment and their relationship to learning performance. We found that the previously identified ROI‐based patterns correlated with learning performance in the prospective normal (P < 0.01) and untreated PD (P < 0.05) cohorts. Voxel analysis revealed that target retrieval was related to a network characterized by bilateral activation of the dorsolateral prefrontal, premotor and anterior cingulate cortex, the precuneus, and the occipital association areas as well as the right ventral prefrontal and inferior parietal regions. Target acquisition was associated with a different network involving activation of the caudate, putamen, and right dentate nucleus, as well as the left ventral prefrontal and inferior parietal areas. Antiparkinsonian therapy gave rise to changes in retrieval performance that correlated with network modulation (P < 0.01). Increases in network activation and learning performance occurred with internal pallidal deep brain stimulation (GPi DBS); decrements in these measures were present with levodopa. Our findings suggest that network analysis of activation data can provide stable descriptors of learning performance. Network quantification can provide an objective means of assessing the effects of therapy on cognitive functioning in neurodegenerative disorders. Hum. Brain Mapping 11:197–211, 2003.


Annals of Neurology | 2002

Pallidal stimulation for Parkinsonism: Improved brain activation during sequence learning

Masafumi Fukuda; Maria Felice Ghilardi; Maren Carbon; Vijay Dhawan; Yilong Ma; Andrew Feigin; Marc J. Mentis; Claude Ghez; David Eidelberg

We used 15O‐labeled water and positron emission tomography to assess the effect of deep brain stimulation of the internal globus pallidus on motor sequence learning in Parkinsons disease. Seven right‐handed patients were scanned on and off stimulation while they were performing a motor sequence learning task and a kinematically matched motor execution reference task. The scans were performed after a 12‐hour medication washout. Stimulation parameters were adjusted for maximal motor improvement; experimental task parameters were held constant across stimulation conditions. Internal globus pallidus stimulation improved motor ratings by 37% (p < 0.01). During the sequence learning task, stimulation improved performance as measured by several correct anticipatory movements (p < 0.01) and by verbal report (p < 0.001). Concurrent positron emission tomography imaging during learning demonstrated significant (p < 0.01) increases in brain activation with stimulation in the left dorsolateral prefrontal cortex, bilaterally in premotor cortex, and in posterior parietal and occipital association areas. Stimulation did not affect the activity of these regions during the performance of the motor execution reference task. These findings suggest that internal globus pallidus deep brain stimulation can enhance the activity of prefrontal cortico‐striato‐pallidothalamic loops and related transcortical pathways. Improved sequence learning with stimulation may be directly related to these functional changes.


IEEE Engineering in Medicine and Biology Magazine | 1992

Parallel processing of direction and extent in reaching movements

James Gordon; Maria Felice Ghilardi; Claude Ghez

Summary form only given. Reaching movements, in which the hand is moved to a target location, require a sensorimotor transformation; the intended path, initially specified in extrinsic coordinates, must be transformed into a set of intrinsic coordinates that specify a pattern of muscle activation that will bring the hand to the target. A common framework for studying how the nervous system achieves this transformation is derived from robotics; it assumes a series of intermediate stages, including inverse kinematics and inverse dynamics computations. Experiments to characterize the coordinate systems in which reaching movements are planned and to determine whether serial computational strategies are used for planning hand trajectories are described. >


Journal of Neurophysiology | 1995

Control of limb dynamics in normal subjects and patients without proprioception

Robert L. Sainburg; Maria Felice Ghilardi; Howard Poizner; Claude Ghez


Cold Spring Harbor Symposia on Quantitative Biology | 1990

Roles of proprioceptive input in the programming of arm trajectories.

Claude Ghez; James Gordon; Maria Felice Ghilardi; C. N. Christakos; Scott E. Cooper

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James Gordon

University of Southern California

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Maren Carbon

North Shore-LIJ Health System

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Vijay Dhawan

United States Department of Veterans Affairs

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Andrew Feigin

The Feinstein Institute for Medical Research

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