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Biomedical subjects

B Wild

Publications and source records attributed to B Wild.

34 records · Page 2Linked to original sources
PubMed1997

Cerebellar hypermetria: reduction in the early component of the antagonist electromyogram.

Several articles have described the electromyographic (EMG) patterns underlying cerebellar hypermetria. However, the description of the EMG associated with hypermetria is not consistent between studies. It is hypothesized that the reason for this concerns the criteria used to define and describe the antagonist latency. Several studies on neurologically normal individuals have shown that there are two components to the antagonist EMG: an early component and a late component. However, many studies have identified only one component and have not defined whether it was the early or late component. A reanalysis of one published data set that had previously identified only one antagonist component was performed. The reanalysis suggests that hypermetria can be caused by an absence of an early antagonist EMG component, a delayed late component, or both. In addition, a new measure is suggested that allows this hypothesis to be further evaluated.

Cerebellar Diseases↗
PubMed1996

Acceleration deficit in patients with cerebellar lesions. A study of kinematic and EMG-parameters in fast wrist movements.

Slowness of goal-directed movements is a frequent symptom following cerebellar lesions. So far it has not been demonstrated whether this slowness represents compensation for impaired braking which is a feature of cerebellar dysfunction with the consequence of hypermetria, or whether it is an independent part of cerebellar movement disorder. To resolve this question we tested 18 cerebellar patients in a paradigm where they not only had to perform fast goal-directed wrist flexion movements (amplitudes 5 degrees and 30 degrees) but also wrist flexion movements as fast and large as possible without particular target. In normals antagonist activity is minimal in large movements without target. Although subjects were clinically only mildly affected they regularly showed a 'slowness of movement' resulting from a reduction of peak acceleration. This in turn was due to the reduced generation of agonist activity. Peak velocity was not significantly decreased because the acceleration phase was adequately prolonged. Since these changes were most pronounced in the 'fast' movements without target the compensation hypothesis should be discarded. The reduction of acceleration must at least partially be due to a genuine cerebellar deficiency in the fast generation of agonist activity.

Adolescent↗
PubMed1993

Cerebellar ataxia in ataxic hemiparesis? A kinematic and EMG analysis.

It has recently been proposed that the ataxia in ataxic hemiparesis is a clumsiness common to all patients with hemiparesis and not indicative of any involvement of corticopontocerebellar or cerebellocortical pathways. In disagreement with this view, we report here that a patient with ataxic hemiparesis, following a lesion of the corona radiata, showed the disorders in kinematic and electromyographic (EMG) parameters of goal-directed movements that have recently been demonstrated to be characteristic of patients with cerebellar lesions. This suggests involvement of corticopontocerebellar or cerebellocortical pathways in ataxic hemiparesis.

Adult↗
PubMed1991

Cerebellar dysmetria at the elbow, wrist, and fingers.

1. The objective was to investigate in cerebellar patients with dysmetria the kinematic and electromyographic (EMG) characteristics of large and small movements at the elbow, wrist, and finger and thereby to determine the nature of cerebellar dysmetria at distal as well as proximal joints. Flexions were made as fast as possible by moving relatively heavy manipulanda for each joint to the same end position through 5, 30, and 60 degrees. 2. In normal subjects flexions at all joints were accompanied by similar triphasic EMG activity. Movements of increasing amplitude were made with increasing movement durations and increasing durations and magnitudes of initial agonist EMG activity. Antagonist activity often appeared to have two components: one coactive with the initial agonist burst but starting later, the other reaching its peak at about peak velocity. 3. Cerebellar patients with dysmetria showed hypermetria followed by tremor at all three joints when movements were made with the manipulanda. Hypermetria was most marked for aimed movements of small amplitude (5 degrees) at all joints. 4. A characteristic of cerebellar disordered movements, which could be present at all amplitudes and all joints, was an asymmetry with decreased peak accelerations and increased peak decelerations compared to normal movements. Both the asymmetry and the hypermetria for small amplitude movements could be used clinically as sensitive indicators of cerebellar dysfunction. 5. The EMG abnormalities accompanying hypermetria and asymmetry were a more gradual buildup and a prolongation of agonist activity and delayed onset of antagonist activity.(ABSTRACT TRUNCATED AT 250 WORDS)

Aged↗
PubMed1965

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Interprofessional Relations↗
PubMedDate not supplied

The consequence of nucleotide substitutions in the triosephosphate isomerase (TPI) gene promoter.

Mutations at -5A-->G, -8-->GA within the cap proximal element (CPE), and -24T-->G within the TATA box of the triosephosphate isomerase (TPI) gene promoter have been identified in populations with a wide geographical distribution. These mutations lie within, or in close proximity to, known cis-active elements in the TPI gene promoter. To determine the functional significance of mutation at these sites, which remains controversial, their effect on the expression of erythrocyte TPI enzyme activity was studied in 110 healthy unrelated subjects. The -5G mutation did not alter erythrocyte TPI level, whereas the -8A mutation was accompanied by a significant reduction in enzyme activity to around 90% and 76% of normal erythrocyte TPI activity in heterozygotes and homozygotes, respectively. The -8A -24G genotype was associated with 75% of normal TPI activity in a heterozygote studied, implying that substitution of G at position -24 within the canonical TATA motif causes an additive decrease in TPI gene transcription in erythroid cells. A DNA-protein complex of 125kDa which was competitively blocked by specific unlabelled oligomers was demonstrated at the CPE and TATA box by electrophoretic mobility shift analysis. These findings provide direct evidence that TPI promoter mutations are linked to a reduction of TPI enzyme activity in vivo.

Binding Sites↗
PubMedDate not supplied

Goal post injuries in soccer. A laboratory and field testing analysis of a preventive intervention.

Soccer is the most popular team sport worldwide, with approximately 40 million amateur participants. Most fatalities in soccer are related to player impact with the goal post. This study focuses on two case reports, a laboratory testing phase, and a pilot field testing phase of preventive equipment that can be used around the goal to prevent injury. Horizontal and vertical impact testing in the laboratory revealed impact force was diminished when the goal post was covered with protective padding (reduction of 31% and 63%) (P < 0.05). These data showed a statistically significant decrease in force at all temperatures. In the pilot field testing phase of the study, 471 games were monitored. Soccer teams participating in youth, teen, and adult soccer leagues were included in this phase of the study. During the 3-year study, there were seven player collisions with padded goal posts, and no injuries were recorded. The use of padded goal posts within the game of soccer has been documented to reduce the possibility of injury, both in the laboratory phase and in the pilot field testing phase.

Athletic Injuries↗