Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P50583 (asymmetrical)
 12,197 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1) Etiology of convulsions starting prior to two years of age was discussed in 418 cases. Neonatal seizures before 30 days old appeared in 86 cases (53 boys and 33 girls). Three hundred and thirty-two patients (172 boys and 160 girls) had convulsions in infancy. Twelve patients (9 boys and 3 girls) suffered from convulsions both in neonatal and infantile period. 2)Etiology of convulsions was prenatal in 67 cases (16%), natal in 49 cases (12%), postnatal in 158 cases (38%) and unknown in 144 cases (34%). Prenatal factors consisted of cerebral malformation (23 cases, 6%), associated physical minor anomaly such as cataracta or finger abomaly (11 cases, 3%), abnormal pernatal history (8 cases, 2%), congenital heart disease 3) cases, 1%), tuberose scleorsis (7 cases, 2%) and positive family history (13 cases, 3%). Postnatal causes included hypocalcemia or hypoglycemia (7 cases, 2%), brain tumors (3 cases, 1%), breath-holding spells (21 cases, 5%), febrile convulsion (44 cases, 11%), bathing (3 cases, 1%), afebrile colds (3 cases, 1%), purulent meningitis (17 cases, 4%), DPT immunization (10 cases 2%), vaccination (7 cases, 2%) and acute hemiplegia (10 cases, 2%). The group of unknown etiology were as fns (38 cases, 9%), epilepsy associated with interictal signs (23 cases, 6%), benign infantile convulsions (57 cases, 14%), neonatal convulsion of unknown etiology (12 cases, 3%) and miscellaneous categories (4%). 3) Pregnancy was abnormal in 53% of cases with cerebral malformation. Asphyxia at birth was noted in 43% of patients with tuberose sclerosis and in 35% of congenital cerebral abomaly. 4) Pneumoencephalographic examinations revealed midline anomaly in 50% of cerebral malformation. It was abnormal in all cases with tuberose sclerosis, head injury and epilepsy with interseizure neurological signs. 5) There were no correlations between the seizure pattern and the etiology in neonatal convulsion. In infancy, focal-unilateral convulsions and infantile spasms were frequently associated with organic damages. Generalized seizures were seen in organic lesions as well as functional ones although approximately half of the cases were febrile convulsion, benign infantile convulsion or breath-holding spell. 6) EEG features of cerebral malformation were asymmetrical or multifocal dischages in neonatal period and hypsarhythmia or focal-unilateral spike discharges in infancy. Tuberose sclerosis showed hypsarhythmia in infancy. In birth injury or cerebral anoxia, EEG mostly revealed focal-unilateral abnormality or suppression-burst activity in newborns and hypsarhythmia or focal features in infants. 7) The occurrence rate of neonatal seizures in autopsy cases with intracranial pathology was demonstrated. EEG with intravenous diazepam was useful to know pathophysiology of infantile spasms.
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PMID:Etiology of convulsions in neonatal and infantile period. 99 19

A brief application of high K+ or excitatory amino acids (i.e. kainic acid) generated repetitive synchronized burst that persisted for the duration of the application, in the CA3 field. Once excitability has been enhanced, further stimulation of various inputs evoked burst instead the typical excitatory postsynaptic potential--inhibitory postsynaptic potential sequence evoked in control conditions. These long-lasting changes in synaptic efficacy involved the activation of glutamate receptors of N-methyl-D-aspartate (NMDA) subtype. A brief period of hyperactivity (i.e. kindling of limbic pathways or administration of kainic acid) also resulted in a more delayed synaptic remodeling, notably of hippocampal mossy fibers (i.e. the axons of granule cells that mostly contact the apical dendrites of CA3 pyramidal neurons). Thus mossy fibers sprouted and made multiple ectopic asymmetrical synapses with spines of both granule cells dendrites and basilar dendrites of CA3 pyramidal cells. Finally, sprouting of mossy fibers was associated with a significant rise in the density of kainic acid binding sites (fmol/mg tissue) in the aberrantly innervated zones: the inner third of molecular layer and the stratum oriens of CA3. Saturation studies revealed that this rise did not significantly affect the affinity (Kd values) but the Bmax. In conclusion, brief seizure episodes produced in the hippocampus remarkably long-lasting changes in synaptic efficacy; synaptic density and the mean density of excitatory amino acid receptors of non-NMDA subtype. The role that such plastic changes may play in the permanence of the epilepsy is finally discussed.
Epilepsy Res Suppl 1992
PMID:Long-term potentiation and sprouting of mossy fibers produced by brief episodes of hyperactivity. 133 65

EEG frequency and time domain color maps were computed during amygdala kindling in cats. The pattern of the amygdala afterdischarge (AM/AD) propagation to the cortex was assessed as kindling evolved. Our results show that the AM/AD has 4 components that coincide with the activation of certain cortical areas during specific behavioral stages. The pattern of the cortical projection follows an asymmetrical temporo-fronto-occipital direction, the ipsilateral temporal lobe being the first activated zone, followed by the ipsilateral and contralateral prefrontal areas. The contralateral temporal activation is a late phenomenon. We conclude that the electrographic and behavioral manifestations of this model of complex partial epilepsy are asymmetrical during the whole process, including the convulsive stage.
Epilepsy Res 1992 Oct
PMID:EEG frequency and time domain mapping study of the cortical projections of temporal lobe amygdala afterdischarge during kindling in the cat. 147 95

The distribution and synaptic connections of dopamine axons were studied by light and electron microscopy in human cerebral cortex. For this purpose, dopamine immunoreactivity was characterized in apparently normal anteriolateral temporal cortex, which was removed to gain access to the medial temporal lobe during tumor excision or treatment of epilepsy. Nissl sections showed this to be granular neocortex. Dopamine fibers were distributed throughout this cortex, although there were relatively more fibers in layers I-II and in layers V-VIa, compared to layers III-IV and VIb, resulting in a bilaminar pattern of labeling. In all layers, fibers were seen to form numerous varicosities, and to vary in size from thick to very fine. Fibers were relatively straight, sparsely branched and were oriented in various planes within the cortex. However, in layer I, they often ran parallel to the pial surface. In order to analyze the functional interactions of dopamine fibers, individual cortical layers were surveyed for dopamine synapses. These were usually symmetrical (Gray's type II), although 13% of them were asymmetrical. Approximately 60% of dopamine synapses were made with dendritic spines, and 40% with dendritic shafts, and this ratio was similar in all layers. On both spines and shafts, it was common to see dopamine synapses closely apposed to an unlabeled asymmetric input, suggesting a dopamine modulation of excitatory input. Some postsynaptic dendritic shafts had features of pyramidal cells, including formation of spines. Since pyramidal cells are the major type of cortical spiny neuron, they probably represent the main target of dopamine synapses in this cortex. There were also dopamine profiles apposed to membrane densities on unlabeled axon terminals, suggesting another type of synaptic interaction. These findings provide the first documentation of dopamine synapses in the human cortex, and show that they form classical synaptic junctions. The location of these synapses on spines and distal dendrites, and their proximity to asymmetric synapses, suggest a modulatory role on excitatory input to pyramidal cells.
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PMID:Light and electron microscopic characterization of dopamine-immunoreactive axons in human cerebral cortex. 150 72

The role of interhemispheric pathways in generalization of partial seizures was evaluated in the kindling model of epilepsy. The generalized seizure kindled from the amygdala was asymmetrical in cats with callosal bisection, destruction of massa intermedia of the thalamus or bilateral ventral hippocampus. The generalized convulsion of amygdala kindled cats became asymmetrical or changed into partial seizures by callosal bisection. The fully-kindled amygdala seizure of a split-brain epileptic baboon and rhesus monkey was a hemiconvulsion or an asymmetrical generalized convulsion. The amygdala-kindled bisymmetrical generalized convulsion of the epileptic baboon was changed into a hemiconvulsion or an asymmetrical generalized convulsion. These results indicate that the corpus callosum plays an important, although not exclusive, role in bilateralization of epileptic activity, and its role becomes more important when the animal ascends the phylogenetic scale.
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PMID:The role of interhemispheric pathways in generalization of kindled seizures in cats and subhuman primates. 176 5

In the paper the analysis is given of "penicillin" epilepsy in animals (cats) in conditions of different forms of deafferentation of one of the halves of the fore brain. It is shown, that in conditions of combined section of one half of the operculum of the midbrain and commissural systems of the endbrain, diencephalon and midbrain, under large doses of penicillin, unilateral convulsive activity is recorded in summate electrical activity of one of the brain halves at the side of the midbrain lesion. After the completion of unilateral organization of the epileptic process an asymmetrical sleep takes place: at the side, at which epileptiform activity was recorded, a more deep phase of the sleep appears than in the opposite brain half.
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PMID:[Unilateral epilepsy and the asymmetry of postepileptic sleep]. 216 98

In 64 epileptics (mean age 35.7 years, mean onset of the disease at the age of 12.1 years) the author used a test of learning a series of movements (TOSP B). It involves the performance of a series of three asymmetrical movements maximal speed of learning is evaluated. Patients with epilepsy have a significantly reduced rate of motor learning, as compared with two comparable group of healthy subjects (104 and 67 subjects). Patients with a favourable course of the disease (n = 24) are significantly quicker than patients with an adverse development of the disease (n = 40). The author discusses the revealed significant correlation with the duration of the disease, contact with psychiatry, later onset of the disease, IQ and education, Contrary to expectations, the correlation with age was not significant, the factor of the disease being more important than the factor of ageing. Tests of asymmetrical movements are sensitive for the detection of relatively subclinical symptoms of cerebral affections. They prove useful as a stable part of neuropsychological examinations in epileptic patients.
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PMID:[Epilepsy and the speed of learning motor skills]. 259 82

Lateralization of the epileptic process in a group of 152 subjects and the relationship of epilepsy to the lateralization of brain functions was studied in smaller groups of 108 and 56 subjects. A unilateral epileptic process in the temporal limbic structures of the brain is localized in the left half of the brain twice (in 64.5%) to four times (in 80.8%) as often as in the right half. The greater the asymmetry of physiological brain functions--in particular motor and verbally symbolic functions--the more is this tendency pronounced. An epileptic process in temporal limbic structures of the left half of the brain is manifested more often in primarily generalized epileptic seizures with initial sudden and complete loss of consciousness. Episodic spike-and-wave activity, which is the typical electroencephalographic correlate of primarily generalized seizures, or of the thalamocortical aetiopathogenetic component of the epileptic process, is often asymmetrical in amplitude, which in 68.1% of these cases is twice as high over the left hemisphere. An epileptic process in subcortical structures of the right hemisphere impairs physiological asymmetry of emotive facial mimicry (with preponderance of mimic reactions on the left) and in 68.4% of the cases causes atypical preponderance of emotive mimicry in the right half of the face. A unilateral epileptic process in subcortical structures of the left half of the brain has a more favourable course and more hopeful prognosis in 70.4% of the cases, while the course of a right-sided process is worse in 67.6%.
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PMID:Physiological asymmetry of brain functions--its influence on the lateralization, symptomatology and course of the epileptic process. 294 6

A multimodal evoked potential study was realised in three groups of children or adolescents 5 to 15 years old. The first group included 25 normal non-epileptic subjects; the second group was composed of 27 subjects with partial idiopathic epilepsy (PIE) (benign childhood epilepsy with centro-temporal spike; childhood epilepsy with occipital paroxysms); the third group was formed of 20 subjects with partial symptomatic epilepsy (PSE) without patent anatomical lesion or with anatomical lesion. Recording for each subject included: flash visual evoked potentials, pattern visual evoked potentials, brainstem auditory evoked potentials and somatosensory evoked potentials. Each curve obtained was studied for the response morphology, the measure of the different wave latencies, the inter-peak latencies (conduction time) and the amplitudes. A statistical treatment of the data was performed to evaluate the significance of variation of the different parameter values obtained for the various groups. Among the significantly modified parameters, we found: an increase of the amplitudes in the PIE and a decrease in the PSE, specially when an anatomical lesion exists; an asymmetrical amplitude of the somatosensory responses in the PIE with centro-temporal spike; an increase of the central somatosensory conduction time in the PSE with anatomical lesion.
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PMID:[Multimodal evoked potentials in partial epilepsy in children]. 313 71

EEG examinations were carried out on 137 patients with thalidomide embryopathy aged between 7 and 22 with a mean age of 17.0. Waking and sleep EEGs were normal in 82 (59.9%), and abnormal in 55 (40.1%). The incidence of abnormal EEG was significantly high in the patients associated with mental retardation, and it increased in proportion to the severity of mental retardation. The most frequent abnormal EEG finding was slowing of the basic activity (35/137; 24.8%). The incidence of slowing was significantly higher in the patients with a sensorineural hearing impairment (26/74; 35.1%) than in those with dysmelia (9/62; 14.5%). Slowing appeared frequently in the patients with various cranial nerve symptoms (30/84; 35.7%). The incidence of slowing was found significantly high in the patients with borderline or subnormal intelligence (8/16; 50.0%), and it correlated with the severity of mental retardation. Many patients (48/84; 57.1%) showed unilateral or asymmetrical neurological symptoms. However, asymmetry or focal abnormality in EEG was shown in only 8 patients. Positive spikes appeared frequently in the patients with gonadal dysplasia. Other somatic symptoms, past medical history and family history were not related to the incidence of abnormal EEGs. Eight patients had had epileptic seizures prior to this examination. Another 2 patients had nocturnal enuresis and showed epileptic EEG abnormalities in this examination. The incidence of epilepsy was significantly higher in the patients we examined than among the general population. It is concluded that ingestion of thalidomide during pregnancy affected not only the morphological development of the limbs of the fetus, but the functions of its central nervous system, causing hearing impairment, other cranial nerve symptoms, mental retardation or epilepsy.
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PMID:Electroencephalographic study of 137 patients with thalidomide embryopathy. 343 8


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