Responses evoked by stimulation of the acoustic pathway during the sleep-wakefulness cycle.
Explore the source record for details and available documents.
Biomedical subjects
Publications and source records attributed to E Favale.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Normative data concerning the waves W1, W2, W3, P4, N5, P6 and N7 recorded from the scalp after stimulation of the infraorbital nerve have been collected from 96 healthy subjects, selected according to age and sex. Peak latency, inter-peak intervals, side-to-side asymmetry of inter-peak intervals, amplitude, amplitude ratio of some components versus W1 and side-to-side asymmetry of such ratio have been analysed as functions of age and sex. None of these parameters appeared to be affected by sex; computation of the correlation coefficient showed a significant (P less than 0.01), though slight, increase of value of the inter-peak intervals W1-W2 and W1-W3 with age. This increase was partially confirmed by analysis of variance. However, such differences are too small to be useful for practical applications, so only a single normative value is proposed for each parameter. The influence of stimulus strength on the amplitude of the W1 component has been studied in 10 more subjects; amplitude saturation of this wave has been found to take place at intensities between 4 and 6 times the sensory threshold. Increasing the stimulus rate from 1 to 3 pulses/sec did not affect any of the components. It is remarked that components W1, W2, W3 and, to a lesser extent, P4 are the ones to be considered useful in clinical practice.
Early scalp responses evoked by stimulation of the infraorbital nerve (W1, W2, W3) have been investigated in 23 patients affected by tumours of the base of the skull (parasellar area and cerebello-pontine angle) and in 38 patients suffering from 'idiopathic' trigeminal neuralgia. Differences in conduction times between healthy and affected side were evaluated and confronted with data obtained from 30 normal volunteers. Alterations of the response were found in all the patients with tumours of the base of the skull who had clinical signs in the trigeminal area and in 7 of the 12 cases without such signs. The usual pattern of alteration in cases with tumours of the parasellar area was a parallel involvement of W2 and W3 (both absent or delayed to the same extent), whereas in tumours of the cerebello-pontine angle W3 was more seriously affected than W2. Wave W1 was never altered. Pre- and post-operative recording sessions in 2 patients showed definite improvement of the responses after removal of the tumour. In 9 patients suffering from 'idiopathic' trigeminal neuralgia delays of conduction were found on the painful side, suggesting that damage to the trigeminal root, possibly at its entry zone into the pons, had taken place. Retrogasserian injection of glycerol was performed in 12 of the 38 patients with trigeminal neuralgia. Stimulation of the operated side showed disappearance of W2 and W3 in 9 cases, prolonged W1-W3 interval in 2 cases and no alterations in 1 case. The extent of response alteration usually paralleled the clinical results.
In 25 healthy volunteers the supraorbital nerve was stimulated and evoked potentials were recorded. Leads were placed on the scalp and along the ipsilateral eyebrow-mastoid line and were either referred to a non-cephalic reference (on the neck, or Cv7) or linked to form bipolar derivations. As template wave form was chosen the one obtained from derivation Cz-Cv7, which had an initial triphasic component with negative (SW1a), positive (SW1b), negative (SW1c) polarity (mean latencies 0.63, 0.95 and 1.43 msec), followed by 2 negative waves (SW2 and SW3, mean latencies of 2.20 and 2.89 msec). A final positive wave could be observed in most cases (SP4, mean latency of 4.08 msec). The records collected from the various derivations showed that each component (SW1, SW2, SW3 and SP4) had a different behaviour, thus suggesting separate origins. SW1 would originate from a volley travelling from the point of stimulation towards the mastoid, probably across the ophthalmic branch of the trigeminal nerve. The subsequent components would be generated by deeply situated structures: double pulse stimulation suggests that SW1, SW2 and SW3 are generated before the first synapse, whereas SP4 is a postsynaptic event. A strong similarity exists between the components evoked by stimulation of the supraorbital and the infraorbital nerves. Local anaesthetic block of the frontal nerve on the stimulated side and monitoring of the EMG activity of m. orbicularis oculi and m. frontalis ruled out any muscle contamination of the responses described in this paper.
Cervical, parietal and prerolandic somatosensory evoked potentials (SEPs) to median nerve stimulation at the wrist were recorded with an earlobe reference in 24 patients with Huntington's disease (HD) and in 24 age-matched normal controls. Cortical responses of abnormal wave form and reduced amplitude were constantly observed in HD patients. SEP changes affected more severely the prerolandic (P22/N30) pattern, which could not be recognized in two-thirds of patients, than the parietal (N20/P27) pattern, which could be identified in all cases. The N20 latency and the central conduction time (N13-N20 interval) were significantly increased. The occurrence of abnormalities of central conduction and of a predominant involvement of the prerolandic SEP pattern suggests an impairment of impulse transmission along the somatosensory lemniscal pathway at subcortical, possibly thalamic, level in HD.
To validate a procedure assembling CT scans in a three-dimensional (3D) array, the interindividual variability of cranioencephalic relationships, as estimated by our technique, was compared with that of the normal population. To this purpose the position of the habenulopineal complex (HPC) with respect to skull references was investigated in 41 normal subjects. In particular the x, y, and z, coordinates of individual HPCs were determined after each CT was assembled in a 3D multislice array. Thereafter, distances of the HPC from the frontal and occipital poles, the vault, and the base of the skull were measured and compared with the anatomicoradiological norms. From our estimates the distances of the HPC from both the frontal pole and the vault of the skull proved to vary as a function of the maximal skull diameter with no distortion of cranioencephalic relationships. The proposed assembling method can be regarded as a reliable tool for a quantitative evaluation of data collected from CT or other reconstructive tomography techniques in anatomicoclinical studies. This method enables a generalized (i.e., not confined to neurosurgical procedures) application of stereotactic principles.
The occurrence of epileptic seizures was investigated in 141 patients with angiographically proven carotid or MCA occlusive disease. Epileptic seizures occurred some time during the clinical course of the disease in 17.3% of carotid patients and in 10.8% of MCA patients, being mainly represented by partial motor seizures. The pattern of occurrence of seizures in the natural history of cerebral arterial disease was different in the two groups. In the carotid group, epilepsy was the presenting symptom in 6.7% of patients, whereas no MCA patient had seizures prior to the appearance of a neurological deficit. Since epileptic seizures may complicate an otherwise asymptomatic carotid obstruction, angiography should be performed whenever the other standard investigations, including CT-scan, fail to reveal the cause of late-onset epilepsy.
Explore the source record for details and available documents.