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Biomedical subjects

S Trueman

Publications and source records attributed to S Trueman.

4 recordsLinked to original sources
PubMed1995

Monopolar needle evaluation of paraspinal musculature in the cervical, thoracic, and lumbar regions and the effects of aging.

Motor unit characteristics (phases, turns, amplitude, duration, and area) were measured using a monopolar needle and narrowed bandpass (500 Hz to 10 kHz) in cervical, thoracic, and lumbar paraspinal muscles in 66 subjects (36 women and 30 men) aged 22-81 years (mean age 45.7 years). Cervical motor units were of lower amplitude and area than thoracic and lumbar motor units (P = 0.0001), respectively. The durations of lumbar motor units were longer and larger than cervical and thoracic motor units (P = 0.0004). Analysis of covariance of the measured characteristics against age showed no significance in the cervical and thoracic regions. In lumbar paraspinal motor units, phases and turns increased significantly with age (P = 0.044 and P = 0.016, respectively). The increase was < 1.0 phase over 30 years. Motor unit amplitude increased with aging (P = 0.055) showing an increase of 360 microV over a 30-year time period. It is appropriate to assess the number of phases and turns, as well as the duration of the motor units in the cervical and thoracic (but not lumbar) spines in addition to seeking evidence of spontaneous, single fiber discharges.

Adult↗
PubMed1993

Receiver operating characteristic curve analysis in the prediction of carpal tunnel syndrome: a model for reporting electrophysiological data.

Receiver operating characteristic (ROC) curves were used to predict the risk of carpal tunnel syndrome (CTS). Patients were classified clinically as: (1) normal exam and no symptoms (169 hands); (2) having a motor and/or sensory deficit typical of CTS (115 hands); (3) having a history characteristic of CTS (156 hands); and (4) nondiagnostic symptomatology (122 hands). Electrophysiological studies consisted of median and ulnar motor, sensory, and palmar measurements. Group mean values for group 1 differed significantly from groups 2 and 3 (not 4) for all measurements, but values overlapped considerably. Median distal motor latency (DMML) combined with median-ulnar palmar latency differences (MUPLD) had significantly superior discriminant power than other measurements and correlated highly for all groups (r values = 0.71-0.73). These variables were used to construct ROC curves and prediction tables. The approach used allows one to assign a percentage risk of having a CTS and can be used in outcome studies.

Adult↗
PubMed1976

Serological relatedness of herpes simplex viruses. Type-specificity of antibody response.

The serological relatedness of forty-seven strains of type 1 and type 2 herpes simplex virus was investigated by reciprocal and non-reciprocal neutralization kinetics. Early rabbit antisera divided the virus strains into two distinct groups where confident indentification of virus type was possible. Hyperimmune mouse and rabbit antisera did not divide the two virus types into two distinct non-over-lapping groups. The extent of overlap varied with the particular attribute of the virus being studied. The virus types were best discriminated by their neutralizability by type 1 antisera and least well by their neutralizability by type 2 antisera. The results of reciprocal kinetic neutralization test with hyperimmune mouse antisera were analysed by multi-dimensional cluster analysis. Hyperimmune mouse or rabbit antisera could not be discriminated with respect to their immunogenic type by their absolute neutralization rate constants against either type 1 or type 2 virus, but could be distinguished on a group basis by their relative neutralizability against both virus types (antiserum specificity attribute); however, using this latter criterion, the type of immunogen could only be predicted in seven of the forty antisera under test. 'Early' mouse antisera could also be distinguished as groups by their absolute k-values against type 1 herpes virus. Thus, immunogenic identification, on other than a group basis, was unreliable. The specificity of a given serum was inversely related to its titre. There was a positive correlation between the specificity of a given virus strain and of its corresponding antiserum.

Animals↗