Topography of scalp-recorded motor potentials in human finger movements

Four distinct negative events were identified in the averaged, scalp-recorded EEGs of normal subjects before and after the onset of self-paced, voluntary finger movements; reaction-time movements and passive movements were also studied. These events are the peak of the negative slope (NS'), the initial slope of motor potential (isMP), the parietal peak of motor potential (ppMP), and the frontal peak of motor potential (fpMP). For self-paced movements, NS' and isMP occurred before the onset of electromyographic (EMG) activity, and ppMP and fpMP occurred after the onset of EMG activity. NS' had a wide distribution, covering the parietal region with slight contralateral predominance. The isMP mapped focally over the contralateral hand motor area on the scalp. The location of ppMP was similar to that of isMP. The fpMP was localized anterior and medial to motor cortex with a contralateral preponderance and possible location over the supplementary motor area. The isMP and fpMP also were identified in the recordings of reaction-time movements, but only the fpMP persisted in the recordings of passive movements. The isMP appears to reflect activation of the cortical cells in the hand area of motor cortex for the execution of voluntary movement, and the fpMP appears to reflect proprioceptive feedback from the periphery.     

What is the Bereitschaftspotential?

Since discovery of the slow negative electroencephalographic (EEG) activity preceding self-initiated movement by Kornhuber and Deecke [Kornhuber HH, Deecke L. Hirnpotential?nderungen bei Willkurbewegungen und passiven Bewegungen des Menschen: Bereitschaftspotential und reafferente Potentiale. Pflugers Archiv 1965;284:1-17], various source localization techniques in normal subjects and epicortical recording in epilepsy patients have disclosed the generator mechanisms of each identifiable component of movement-related cortical potentials (MRCPs) to some extent. The initial slow segment of BP, called 'early BP' in this article, begins about 2 s before the movement onset in the pre-supplementary motor area (pre-SMA) with no site-specificity and in the SMA proper according to the somatotopic organization, and shortly thereafter in the lateral premotor cortex bilaterally with relatively clear somatotopy. About 400 ms before the movement onset, the steeper negative slope, called 'late BP' in this article (also referred to as NS'), occurs in the contralateral primary motor cortex (M1) and lateral premotor cortex with precise somatotopy. These two phases of BP are differentially influenced by various factors, especially by complexity of the movement which enhances only the late BP. Event-related desynchronization (ERD) of beta frequency EEG band before self-initiated movements shows a different temporospatial pattern from that of the BP, suggesting different neuronal mechanisms for the two. BP has been applied for investigating pathophysiology of various movement disorders. Volitional motor inhibition or muscle relaxation is preceded by BP quite similar to that preceding voluntary muscle contraction. Since BP of typical waveforms and temporospatial pattern does not occur before organic involuntary movements, BP is used for detecting the participation of the 'voluntary motor system' in the generation of apparently involuntary movements in patients with psychogenic movement disorders. In view of Libet et al.'s report [Libet B, Gleason CA, Wright EW, Pearl DK. Time of conscious intention to act in relation to onset of cerebral activity (readiness-potential). The unconscious initiation of a freely voluntary act. Brain 1983;106:623-642] that the awareness of intention to move occurred much later than the onset of BP, the early BP might reflect, physiologically, slowly increasing cortical excitability and, behaviorally, subconscious readiness for the forthcoming movement. Whether the late BP reflects conscious preparation for intended movement or not remains to be clarified.     

Neuromagnetic fields accompanying unilateral and bilateral voluntary movements: topography and analysis of cortical sources.

Movement-related magnetic fields (MRMFs) accompanying left and right unilateral and bilateral finger flexions were studied in 6 right-handed subjects. Six different MRMF components occurring prior to, and during both unilateral and bilateral movements are described: a slow pre-movement readiness field (RF, 1-0.5 sec prior to movement onset); a motor field (MF) starting shortly before EMG onset; 3 separate "movement-evoked" fields following EMG onset (MEFI at 100 msec; MEFII at 225 msec; and MEFIII at 320 msec); and a "post-movement" field (PMF) following the movement itself. The bilateral topography of the RF and MF for both unilateral and bilateral movements suggested bilateral generators for both conditions. Least-squares fitting of equivalent current dipole sources also indicated bilateral sources for MF prior to both unilateral and bilateral movements with significantly greater strength of contralateral sources in the case of unilateral movements. Differences in pre-movement field patterns for left versus right unilateral movements indicated possible cerebral dominance effects as well. A single current dipole in the contralateral sensorimotor cortex could account for the MEFI for unilateral movements and bilateral sensorimotor sources for bilateral movements. Other MRMF components following EMG onset indicated similar sources in sensorimotor cortex related to sensory feedback or internal monitoring of the movement. The results are discussed with respect to the possible generators active in sensorimotor cortex during unilateral and bilateral movement preparation and execution and their significance for the study of cortical organization of voluntary movement.     

Cortical topography of premotor and motor potentials preceding self-paced, voluntary movement of dominant and non-dominant hands.

The cortical potentials preceding movement, negative slope (NS'), premovement positivity (PMP), and the initial slope of motor potential (MP), were studied in detail with a 29-channel averaged EEG mapping technique in normal subjects. Self-paced, voluntary movements of the right and left index fingers were performed up to 150 times, and topographic color maps were created from the averaged wave forms. The maps revealed NS' of the dominant hand on the vertex and NS' of the non-dominant hand on the contralateral centroparietal area. PMP appeared on the ipsilateral precentral area, and the initial slope of MP appeared on a small, distinct contralateral precentral area, presumably the hand motor area. The amplitudes of the potentials did not show significant differences between dominant and non-dominant hands. PMP and the initial slope of MP appeared significantly earlier preceding non-dominant hand movement as compared with dominant movement. The findings indicate some difference in cortical activity relating to dominant and non-dominant hand movement.     

Frontal lobe contribution to voluntary movements in humans

We assessed the contribution of human prefrontal cortex to movement related potentials (MRPs) generated prior to voluntary movements. MRPs were recorded during self-paced movements of the right thumb (experimental condition I), the left thumb (experimental condition II) and both thumbs (experimental condition III) from patients with focal lesions centered in dorsolateral frontal association cortex (PFCx, n = 11) and in age matched controls (n = 11). Controls generated a slowly rising readiness potential (RP) beginning at about 1000 ms prior to movement. A negative shift (NS') began at about 450 ms and a motor potential (MP) appeared at about 100 ms prior to movement. Both the NS' and MP were maximal over scalp sites contralateral to movements. Unilateral PFCx lesions preferentially reduced the RP and NS' components of the MRP. This indicates that PFCx is involved in a neural network beginning at least 1000 ms prior to movement. The differential PFCx effects on the early (RP, NS') and late components (MP) suggest that these MRPs index different movement-related circuits.     

Recording of movement-related potentials from the human cortex

A patient with intractable epilepsy secondary to a brain tumor was evaluated with a chronically implanted array of 64 stainless-steel subdural electrodes covering the perirolandic area. Cortical potentials associated with voluntary, self-paced middle-finger extension were recorded simultaneously from subdural and scalp electrodes using a computer-assisted method for averaging movement-related potential (MRP) in relation to electromyographic (EMG) onset. A high-amplitude negative potential, Bereitschaftspotential/negative slope (BP/NS'), preceding the onset of the EMG activity by more than 1 sec was recorded in an extremely localized fashion exclusively from electrodes placed in the precentral hand motor area as well as in the more medial part of the somatosensory hand area. These results suggest that the hand motor and sensory areas have an essential participation in the generation of MRPs and, therefore, also in the preparation of voluntary finger movements.     

Cerebral potentials preceding unilateral and simultaneous bilateral finger movements.

Cerebral potentials preceding voluntary bilateral simultaneous finger movements were investigated in 19 right-handed young adult subjects, and were compared with unilateral right-sided finger m n the same experiment. With bilateral movements, the Bereitschaftspotential (BP) was not symmetrical or larger over the dominant hemisphere, but surprisingly, it was larger over the minor hemisphere. The BP averaged -3.66 microV (S.D. 1.96) over the left precentral region and -4.82 microV (S.D. 3.73) over the right precentral region in this condition. The difference was significant at 2P less than 0.01. This difference was pronounced in precentral leads but very small and almost missing in parietal leads. The pre-motion positivity (PMP) was well developed and even larger with bilateral than with unilateral (right-sides) movements. At the vertex it averaged +1.33 microV (S.D.4.16) with bilateral movements and only +0.15 microV (S.D. 1.42) with right-sided unilateral movements (2P less than 0.05). With bilateral movements the PMP could be observed in any record, but with unilateral movements it was missing at the left precentral lead, in accordance with previous publications (Deecke et al. 1969, 1976). The motor potential (MP), measured in a bipolar record from left and right precentral leads, was larger with unilateral (-1.25 microV, S.D. 1.33) than with bilateral movements (-0.36 microV, S.D. 0.92). Onset time differences of the BP preceding unilateral and bilateral movements were very small. However, there was a tendency towards earlier onset with unilateral than with bilateral movements (1031 msec, S.D. 358, as compared with 951 msec, S.D. 305). The averaged EMG revealed differences in movement onset. Muscular contraction tended to be earlier in the right than in the left m. flexor indicis in our right-handed subjects, on the average by 16 msec (S.D. 15). With unilateral right-sided movements, the left m. flexor indicis was not silent but showed an abortive mirror activity in the EMG, without visible movement. This activity occurred on the average 50 msec (S.D. 39) later on the non-moving side.     

Independent control of voluntary movements and associated anticipatory postural responses in a bimanual task.

OBJECTIVE: When one hand loads the other arm, EMG responses in the stationary arm anticipate the load. This study used transcranial magnetic stimulation over each hemisphere to clarify the relationship between a voluntary movement on one side and the anticipatory postural response on the other. METHODS: Subjects (n = 7) performed elbow flexion movements of one arm as a reaction-time task. Because subjects' arms were linked, flexion about one elbow resulted in extension force about the other, and an anticipatory response occurred in those elbow flexor muscles. After the 'go' signal and before the predicted onset of EMG, transcranial magnetic stimuli were delivered over one or other motor cortex. RESULTS: Stimulation contralateral to the reaction-time movement delayed the onset of voluntary EMG (46 ms in right biceps, 77 ms left) but did not alter the onset of EMG in the postural arm. Stimulation contralateral to the anticipatory postural response delayed only the postural EMG (left 96 ms, right 52 ms). CONCLUSIONS: Thus, the associated voluntary and postural responses were delayed independently by stimuli over their respective contralateral motor cortex. SIGNIFICANCE: This suggests that, although timing of responses may be linked by an initial signal, the response from each motor cortex develops independently.     

Abnormal movement related potentials in patients with lesions of basal ganglia and anterior thalamus.

Movement-related cortical potentials (MRCPs) were recorded from scalp electrodes during wrist flexion in 15 dystonic patients with bilateral (nine) or unilateral (six) circumscribed lesions in the striatum (eight), pallidum (six), or anterior thalamus (one). The results were compared with those of 10 age-matched healthy volunteers. The early (BP) and late (NS') MRCP components were assessed in terms of their gradients and distribution on the scalp in Cz, C3', and C4'. The gradients of both BP and NS' components were significantly flatter in the patients with bilateral lesions than in the control subjects. Also, the BP gradient was maximum at Cz, and the NS' component was contralaterally predominant in the control subjects but not in the patients. In patients with unilateral lesions, the gradients were flatter (p < 0.05) during movement of the dystonic wrist than during movement of the normal wrist. This difference was significant for BP and NS', regardless of the location of the electrodes. Also, the normal topographic predominance of BP at Cz and of contralateral NS' disappeared. The BP and NS' components of the MRCPs are thought to reflect preparatory activity in the supplementary motor area and the primary motor cortex before movement. Reduced BP and NS' gradients in patients with both bilateral and unilateral lesions of the basal ganglia, which project towards the supplementary motor area, are consistent with this hypothesis. The bilateral nature of these reductions suggests that both the ipsilateral and the contralateral motor cortex are involved in the genesis of the MRCPs and that the dystonia in these patients is associated with impaired motor preparation.     

Temporal relationships of EMG changes preceding voluntary movement to premovement cortical potential shifts

The silent period and a rhythmic slower wave in EMG appear preceding a rapid voluntary movement (Tanii 1984). The present study was performed to investigate temporal relationships of the EMG changes preceding movement to premovement cortical potential shifts, in order to clarify whether the EMG changes are related to preparation and initiation of voluntary movement. A strong push of a hard band with the right wrist was conducted rapidly following a slightly sustained contraction. The surface EMG was detected from the right triceps brachii muscle. The EEG was recorded from C3, Cz and C4. Slowing of the EMG occurred before the movement in addition to the slower wave. The EMG slower waves were accompanied by a negative deflection of raw EEG potentials. The averaged cortical potentials preceding movement fell into 3 negative potentials. The first potential started about 1.0 sec before the EMG burst. Many of the EMG slower waves occurred in the phase of the second potential occurring 330-510 msec before the EMG burst. Premovement silent period appeared in the phase of the third potential occurring 30-60 msec before the EMG burst. Amplitude of these potentials was larger in the contralateral hemisphere than in the ipsilateral one. This asymmetry became statistically significant in the phase of the second potential. The results suggest that the EMG slower waves and the premovement silent period are associated with preparation and initiation of voluntary movement.     

Movement-related cortical potentials in patients with cerebellar degeneration

We studied the topographic distribution of scalp-recorded, averaged movement-related cortical potentials occurring immediately before and after the onset of voluntary movements in six patients with cerebellar degenerative disease. We placed 26 electrodes on the scalp overlying the sensorimotor area and recorded cortical potentials related to abduction of the index finger. The amplitudes and latencies of the potentials were normal in all patients except two, in whom the negative slope (NS') was absent. All patients had an abnormal topographic pattern of potentials compared with normal subjects. The initial slope of motor potential (isMP), which was focal and contralateral in the normal subjects, was diffuse and bilateral in the patients. The topography of the frontal peak of motor potential (fpMP) was more posterior in the patients than in normal subjects. The patterns found in this preliminary study indicate a derangement of sensorimotor cortex activity in voluntary movement as a consequence of cerebellar dysfunction.     

Intermanual Differences in movement-related interhemispheric inhibition

Interhemispheric inhibition (IHI) between motor cortical areas is thought to play a critical role in motor control and could influence manual dexterity. The purpose of this study was to investigate IHI preceding movements of the dominant and nondominant hands of healthy volunteers. Movement-related IHI was studied by means of a double-pulse transcranial magnetic stimulation protocol in right-handed individuals in a simple reaction time paradigm. IHI targeting the motor cortex contralateral (IHI(c)) and ipsilateral (IHI(i)) to each moving finger was determined. IHI(c) was comparable after the go signal, a long time preceding movement onset, in both hands. Closer to movement onset, IHI(c) reversed into facilitation for the right dominant hand but remained inhibitory for left nondominant hand movements. IHI(i) displayed a nearly constant inhibition with a trough early in the premovement period in both hands. In conclusion, our results unveil a more important modulation of interhemispheric interactions during generation of dominant than nondominant hand movements. This modulation essentially consisted of a shift from a balanced IHI at rest to an IHI predominantly directed toward the ipsilateral primary motor cortex at movement onset. Such a mechanism might release muscles from inhibition in the contralateral primary motor cortex while preventing the occurrence of the mirror activity in ipsilateral primary motor cortex and could therefore contribute to intermanual differences in dexterity.     

Enhancement of motor cortical excitability in humans by non-invasive electrical stimulation appears prior to voluntary movement

The time course of facilitation of motor evoked potentials (MEPs) to transcranial electrical stimulation delivered at varying intervals near the onset of a voluntary ballistic movement was studied in 4 normal subjects. MEPs were recorded from the left thenar muscles to unifocal anodal stimulation of the right scalp overlying the hand motor area delivered every 8-10 sec. A click, occasionally associated with the scalp stimulation (P = 0.3-0.6), was the signal for the subject to make a brief thumb press on a piston at short latency. The timing of the scalp stimulus and the click was adjusted so that the former occurred approximately between 100 msec before and 100 msec after the onset of the voluntary movement signaled by the EMG in the thenar muscles. MEPs were not detected when the scalp was stimulated 80 msec or more before onset of voluntary movement and then appeared with increasing probability as the time interval before movement shortened. The amplitudes of MEPs in the 80-40 msec period preceding movement onset were small (less than 20% of maximum) and achieved maximum values 20 msec after movement onset.     

Source analysis of scalp-recorded movement-related electrical potentials

We used brain electric source analysis to study the sources generating the movement-related cortical potentials during the interval from 200 msec before to 200 msec after the movement onset. Dipole solutions were obtained for the peak of the negative slope (pNS′) and the frontal peak of the motor potential (fpMP) on scalp-recorded movement-related electrical potentials elicited by self-paced, repetitive unilateral finger movements in 10 normal volunteers. Two sources in homologous areas on each side of a spherical head model provided a satisfactory solution for the activity occurring at the instant of the pNS′ in all subjects. The fpMP was modeled by a contralateral source and a midline source in 6 subjects and by a single contralateral source in the remaining 4 subjects. The percentage of the residual variance, or goodness-of-fit, over the interval from −200 to 200 msec, using the solutions derived at pNS′ and fpMP, was low. The results support the hypothesis that the NS′ originates from the activity of bilateral generators in the sensorimotor cortex, and the motor potential arises from the combined activity of sources in the contralateral postcentral regions and the supplementary motor area.     

Movement related cortical potentials of cued versus self-initiated movements: double dissociated modulation by dorsal premotor cortex versus supplementary motor area rTMS

The dorsal premotor cortex (PMd) is thought to play a significant role in movement preparation cued by sensory information rather than in self-initiated movements. The evidence in humans for this contention is still circumstantial. Here we explored the effects of modulation of PMd by excitability decreasing 1 Hz repetitive transcranial magnetic stimulation (rTMS) versus excitability increasing 5 Hz rTMS on two forms of movement related cortical potentials: contingent negative variation (CNV) versus Bereitschaftspotential (BP) reflecting externally cued versus self-triggered movement preparation. Ten healthy right-handed subjects performed visually cued or self-triggered simple sequential finger movements with their right hand. CNV and BP were recorded by 25 EEG electrodes covering the fronto-centro-parietal cortex and divided into an early (1500-500 ms before a go-signal or movement onset) and a late potential (500-0 ms). MRI-navigated 1 Hz rTMS of the left PMd resulted in significant increase of the late CNV over the left central region predominantly contralateral to the prepared right hand movement, while 5 Hz rTMS had no effect on CNV. In contrast, 1 and 5 Hz rTMS did not modify BP. Control experiments of 1 Hz rTMS of the supplementary motor area (SMA) and of low-intensity 1 Hz rTMS of the left primary motor cortex did not change CNV, but 1 Hz SMA-rTMS increased late BP. This double dissociation of effects of PMd-rTMS versus SMA-rTMS on CNV versus BP provides direct evidence that the left PMd in humans is more involved in preparatory processes of externally cued rather than self-initiated movements, contrasting with an opposite role of the SMA.     

Theta Burst Stimulation over the human primary motor cortex modulates neural processes involved in movement preparation

ObjectiveTo test whether inhibitory continuous Theta Burst (cTBS) transcranial magnetic stimulation (TMS) can alter neural activity involved in planning and execution of a self-paced movement.MethodsIn seven subjects, cTBS was applied over either the left or right primary motor cortex (left M1 and right M1) and the left dorsal premotor cortex (left PMd) in different experimental sessions. Motor evoked potentials (MEP) at rest were measured as well as the two main components of the movement related cortical potential (MRCP), the Bereitschaftspotential (BP) and the negative slope (NS’), prior to self-paced right thumb opposition.ResultscTBS suppressed contralateral MEPs when it was applied over left M1, right M1 and left PMd. In addition, cTBS over left M1, but not at any other location, reduced the amplitude of the NS’ and tended to shorten the BP onset without changing EMG activity associated with voluntary muscular output. There was a significant correlation between the percent suppression of the MEP and the reduction in amplitude of the total MRCP (BP + NS’).ConclusionscTBS can produce long-lasting effects on brain activity involved in the preparation and execution of a volitional movement.SignificanceThe fact that movement was not compromised while brain activity changed suggests that the motor system of healthy subjects operates with a safety factor that can adjust patterns of activation to compensate for the partial disruption caused by cTBS.     

Neuromagnetic correlates of sensorimotor synchronization

Sensorimotor synchronization tasks, in which subjects have to tap their finger in synchrony with an isochronous auditory click, typically reveal a synchronization error with the tap preceding the click by about 20 to 50 msec. Although extensive behavioral studies and a number of different explanatory accounts have located the cause of this so-called "negative asynchrony" on different levels of processing, the underlying mechanisms are still not completely understood. Almost nothing is known about the central processes, in particular, which sensory or motor events are synchronized by subjects. The present study examined central-level processing in synchronization tasks with magnetoencephalography (MEG). Eight subjects synchronized taps with their right index finger to an isochronous binaural pacing signal presented at an interstimulus interval of 800 msec. To gain information on central temporal coupling between "tap" and "click," evoked responses were averaged time-locked to the auditory signal and the tap onset. Tap-related responses could be explained with a three dipole model: One source, peaking at approximately 77 msec before tap onset, was localized in contralateral primary motor cortex (MI); the two other sources, peaking approximately at tap onset and 75 msec after tap onset, in contralateral primary somatosensory cortex (SI). Temporal coupling of these sources was compared in relation to different trigger points. The second SI source was equally well time-locked to the tap and to the auditory click. Furthermore, analysis of the time locking of this source activity as a function of the temporal order of tap and click showed that the second event - irrespective whether tap or click - was decisive in triggering the second SI source. This suggests that subjects use mainly sensory feedback in judging and evaluating whether they are "keeping time."     

Movement-related potentials accompanying unilateral and bilateral finger movements with different inertial loads.

The present study was aimed at investigating the effect of inertial loading on movement-related potentials (MRPs) recorded from the scalps of normal subjects while performing finger movements. Two experiments were performed. Experiment 1. MRPs preceding and accompanying the execution of voluntary, unilateral finger movements were investigated in 8 subjects under the 3 experimental conditions of: no inertial load, small inertial load (250 g), and large inertial load (400 g). A significant effect of the inertial load on Bereitschaftspotential (BP) amplitude was observed for the 100 msec period preceding movement onset (BP -100 to 0) at precentral electrode sites and following movement onset (N0 to 100) at both precentral and parietal electrode sites. Pairwise comparisons revealed that significant effects were due to differences between the loading and non-loading conditions and not for different amounts of loading. No significant differences were observed for BP onset or early BP amplitudes, indicating that scalp negativity immediately prior to, and during, movement onset is primarily influenced by conditions of inertial loading. Experiment 2. This experiment examined the effect of inertial loading on MRPs for bilateral, simultaneous voluntary finger movements in 10 subjects under conditions of: no inertial load, inertial load applied separately to the left and right fingers, and with identical inertial loads applied to both fingers. No significant effect of inertial load on MRP amplitude was observed. These results are contrasted with those of experiment 1 which show significant effects of inertial loading for unilateral movements and are interpreted in terms of the hypothesis that bilateral movement organization involves 'higher' aspects of motor control than those reflecting adjustment to conditions of inertial loading.     

A cortical slow potential is larger before an isolated movement of a single finger than simultaneous movement of two fingers

Movement-related cortical potentials (MRCPs) preceding voluntary, self-paced, simultaneous extension of the middle and index fingers (two finger movement) were compared with those preceding extension of the index or middle finger alone (single finger movement) of the right hand in 7 right-handed normal subjects. It was meant to double the number of muscles involved in the two finger movement as compared with the single finger movement and to activate only the motor cortex involving the movement of distal joints. The NS' (negative slope) amplitude with the isolated middle finger movement was significantly larger at the precentral area contralateral to the movement as compared with the two finger movement. The NS' amplitude with the index finger movement was also larger than that with the two finger movement at the contralateral precentral area, but the difference was not significant. It is postulated that greater activation of the primary hand sensorimotor area (HSMA) contralateral to the movement might be necessary for the isolated movement of a single finger than for the two finger movement, although a smaller area of HSMA is expected to be activated in the former than in the latter. The NS' may be related to central motor control processes independent of muscle mass activated. As the single finger movement is considered to be more discrete and fine as compared with the simultaneous two finger movement, it is concluded that the HSMA plays an especially important role in discrete and fine finger movement.     

Cortical potential shifts preceding voluntary movement are normal in parkinsonism

We have recorded movement-related cortical potentials (MRCPs) preceding voluntary finger extension from 10 subjects with Parkinson's disease and compared the results with those obtained from groups of young and old subjects described in the previous paper in this volume (Barrett et al. 1986). Three separate potential shifts preceding voluntary movement were identified in the wave forms of all subjects. There were no differences between the healthy aged subjects and those with Parkinson's disease in terms of the onset latencies or gradients of these potential shifts. The potential shift associated with the final phase of preparation (NS') was significantly less widespread over central scalp for the older subjects compared with the young. Equivalent results for a 35-year-old subject with Parkinson's disease were indistinguishable from those obtained from the young subjects suggesting that this restriction in the distribution of NS' is related to normal ageing rather than the disease process of parkinsonism. There were no differences within the group of parkinsonian subjects with respect to potential shifts associated with differing degrees of movement disability between the two hands. Our results contradict previous reports of abnormal MRCPs in Parkinson's disease (Deecke et al. 1977; Deecke and Kornhuber 1978; Shibasaki et al. 1978). We attribute this primarily to an improved method of recording MRCP which compensates for time jitter between EMG onset and the production of a trigger pulse for averaging (Barrett et al. 1985).