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Biomedical subjects

A Autret

Publications and source records attributed to A Autret.

At least 19 recordsLinked to original sources
PubMed1995

Study of unilateral hemisphere performance in children with developmental dysphasia.

Hemisphere specialization for language was studied in 10 children with expressive developmental dysphasia (DD) (mean age 10 years 4 months) submitted to a dichotic listening task (in a word free-recall task and forced-attention task) and a finger tapping/vocalization dual-task paradigm. A nonsense shape dichaptic task was also introduced to control right hemispheric processing. Performances of dysphasic children were compared to those obtained from 15 normal children. The results showed that controls had a right ear advantage in free-recall (words) dichotic listening task and a significant right ear advantage in forced-right-attention task, with a change in ear asymmetry as a consequence of instruction. In the dysphasic group we observed a significant right ear advantage in the free-recall dichotic listening task and no change in ear asymmetry during forced right or forced left condition. Results in time sharing paradigm and nonsense dichaptic task are more difficult to interpret, because there was no interaction between group and condition. These results cannot support a complete left hemisphere dysfunction in developmental dysphasia.

Aphasia↗
PubMed1995

Sleep EEG and developmental dysphasia: lack of a consistent relationship with paroxysmal EEG activity during sleep.

In order to clarify the relationship between developmental dysphasia and EEG abnormalities, paroxysmal activities during sleep were studied in a series of 24 children with expressive developmental dysphasia (mean age 8 years) and compared to a control group of 39 children (mean age 9 years). The children of both groups were selected excluding cases with prior history of neurological disease or epilepsy. In the control group, 37 children had normal sleep EEG while 2 children had paroxysmal abnormalities. In the dysphasic group, epileptic abnormalities were observed in 9 cases, rare in 4 cases and frequent in 5 cases (density: 2.5 to 66.2% of total sleep time). Nevertheless, paroxysmal abnormalities did not reach the frequency described in the Landau-Kleffner syndrome, and it is unlikely that EEG abnormalities could have produced dysphasia.

Aphasia↗
PubMed1994

[Progressive supranuclear paralysis. Quantification of dopamine D2 receptors using radionuclide tomography].

Progressive supranuclear palsy (PSP) may sometimes be misdiagnosed as Parkinson's disease in its early stages, hence an early positive diagnosis of PSP based on dopamine D2 receptor density could be extremely valuable. In the present case report, the absence of dopamine D2 receptors was clearly demonstrated in the striatum using 123I-iodobenzamide (IBZM) tomoscintigraphy. This illustrates the potential use of IBZM tomoscintigraphy to identify Parkinson-like's disease presenting with decreased dopamine D2 receptor density; and hence to predict L-Dopa effectiveness. Further studies are needed to evaluate the vaue of IBZM tomoscintigraphy in the different Parkinson's like diseases.

Aged↗
PubMed1994

[The influence of sleep on abnormal waking movements].

Sleep decreases considerably the abnormal movements seen during waking in the degenerative extra-pyramidal diseases. However, the electrophysiologic recordings reveal that muscular contractions are not completely abolished. This decrease parallels the reduction of the waking system which act likely as a non-specific system of amplification. One can notice that sleep modifies the characteristics of the parkinsonian tremor and that some palatal myoclonias persist during sleep.

Humans↗
PubMed1994

Isolated motor control dysfunction related to progressive multifocal leukoencephalopathy during AIDS with normal MRI.

We describe the case of a human immunodeficiency virus-infected 34-year-old man with progressive multifocal leukoencephalopathy (PML). His case displayed unusual features, including a bizarre movement disorder, predominant involvement of the subcortical U fibers on neuropathologic examination, and the absence of MRI abnormalities suggestive of PML. Anatomic-clinical correlations are discussed.

AIDS Dementia Complex↗
PubMed1993

[Gougerot-Sjögren syndrome. Central neurological involvement with recurrent development].

A 64-year-old woman was repeatedly hospitalized for various recurrent clinical signs of central nervous system involvement. The diagnosis of primary Sjögren's syndrome was established 3 years 6 months after the onset of the disease. Sicca symptoms, as well as inflammatory biological abnormalities were absent. Moreover, both lacrymal and salivary gland secretions were affected. A high level of antinuclear antibodies to SSA and SSB was associated with inflammatory lesions in minor salivary glands biopsy samples consistent with the diagnosis of Sjögren's syndrome.

Antibodies, Antinuclear↗
PubMed1992

Influence of lateral gaze on electroencephalographic spectral power.

The effects of maintaining lateral gaze (as opposed to looking straight ahead) on electroencephalographic spectral power were tested in 12 right handed male subjects during eye opening (EO) and eye closure (EC). Our working hypothesis, based on Kinsbourne's paradigm, was that maintaining right lateral gaze activates the left hemisphere while maintaining left lateral gaze activates the right hemisphere, this activation resulting in a reduction in the spectral power over the hemisphere in question. Results showed that the variations in spectral power involved mainly the alpha frequency band. In the EC condition, the results were consistent with our working hypothesis: right lateral gaze produced a marked reduction in left hemispheric spectral power. In the EO condition, alpha power was constantly higher in the right hemisphere whether lateral gaze was maintained to the right or to the left. This can possibly be due to an attentional effect. Results are discussed with regard of the type of alpha rhythm and of the activation of cortical oculomotor centres. They shed light on the controversy concerning the existence of specific EEG correlates of cognitive activity, which preferentially involve each of the cerebral hemispheres.

Adult↗
PubMed1992

A note on the occurrence of unusual electroencephalographic sleep patterns in selected normal children.

Polysomnographic recordings were performed in 50 children free from any familial or personal history of seizure or neurologic diseases to evaluate the frequency of epileptiform and unusual electroencephalographic patterns in a normal population. A 9-year-old boy exhibited focal spikes that became bilateral with a density of 24% to 32% during slow wave sleep, and another boy showed a few spikes during slow wave sleep. In seven cases, 14- and 6-Hz rhythms were recorded, mostly in rapid eye movement sleep. A right rhythmic and temporal discharge was observed in one girl. Epileptiform electroencephalographic patterns are not infrequent, and 14- and 6-Hz rhythms during rapid eye movement sleep are common in normal children.

Adolescent↗
PubMed1991

Influence of lateralized neuropsychological activities with and without sensorimotor components on EEG spectral power (alpha-rhythm).

Spectral analysis of the EEG (alpha-rhythm) was studied in 8 young right-handed men who underwent 6 experimental tasks which were compared with rest, and included two pure motor activities using only the right and then the left hand, two pure neuropsychological tasks, and two "mixed" tasks with both neurophysiological and motor activities. The electrophysiological parameters studied were the log of spectral power and an asymmetry index (RP-LP)/(RP + LP). In order to demonstrate lateralization of the EEG, one must associate lateralized motor and neuropsychological tasks (which are supposed to preferentially involve one of the cerebral hemispheres). These results may reconcile apparently divergent views published in the literature with respect to lateralized EEG modifications associated with cognitive activities.

Adult↗
PubMed1991

Two mesencephalic lacunar infarcts presenting as Claude's syndrome and pure motor hemiparesis.

Two exceptional cases of mesencephalic lacunar infarcts located both in the anterior vascular territory are reported. In patient 1, the infarct selectively involved the red nucleus, thus resulting in a Claude's syndrome. In patient 2, the lesion was limited to the external 2/3 of the cerebral peduncle, and was responsible for a pure motor hemiplegia (PMH). CT scan easily demonstrated the lesion in both cases. Claude's syndrome is very unusual, and PMH has only been reported once before in a mesencephalic infarct. The reasons why these lesions are so uncommon are discussed.

Aged↗
PubMed1991

[Amineptin dependence and iatrogenic acne. Review of the literature apropos of a case].

We relate the case of a drug addict of 31 years old whose dependence to the amineptine got complicated with severe acne-like lesions, as it sometimes happens. Compared, with teenage acne, severe acne can be distinguished by its late out break, its monstrous nature and its larger surface area. Amineptine has been found (or its metabolites) in the plasma, the urine. The treatment consists in the stopping of the drug addiction, combined with the prescription of isotretinoin.

Acne Vulgaris↗
PubMed1990

[Sleep in neurologic diseases].

Neurological diseases may induce alterations in sleep which are difficult to interpret owing to the multiple interferences introduced by treatments, associated somatic symptoms and time-related changes in causal lesions. The consequences of vascular or traumatic lesions observed in man confirm the data obtained from experimental lesions created in animals, thereby throwing some light on the roles played by the cerebral cortex, the thalamus and the brain stem nuclei. In degenerative diseases polygraphic recordings show subclinical signs of extension which are exceptionally specific of any particular type of degeneration. In epileptic patients recordings have determined the distribution of intercritical activities in the various waking and sleep stages: an increase of the activities during sleep appears to be a fairly independent constitutional feature. To sum up, one may say that the various sleep and waking control systems may be diversely affected by diseases of the nervous system. States of vigilance modulate some critical pathologies, such as epilepsy, according to modalities and a physiopathology that have not yet been fully elucidated.

Brain Injuries↗