نتایج جستجو برای: childhood epilepsy
تعداد نتایج: 216085 فیلتر نتایج به سال:
Glutamatergic neurotransmission governs excitatory signaling in the mammalian brain, and abnormalities of glutamate signaling have been shown to contribute to both epilepsy and hyperkinetic movement disorders. The etiology of many severe childhood movement disorders and epilepsies remains uncharacterized. We describe a neurological disorder with epilepsy and prominent choreoathetosis caused by ...
PURPOSE To examine associations of potentially aetiological significance for the development of pseudoseizures by comparing patients with recent onset pseudoseizures with patients with recent onset epilepsy. METHODS A prospective study of consecutive patients with recent onset pseudoseizures and epilepsy presenting to two Swedish hospitals. Demographic characteristics, somatic symptoms, depre...
The term 'myoclonic epilepsy' is used in adults to describe a form of epilepsy in which a sudden, involuntary, and momentary contraction occurs in a single muscle or muscle group, often without apparent loss of consciousness. Such attacks may occur in isolation, or as part of the pattern of epilepsy in patients experiencing grand mal or other forms of epilepsy. A recent authoritative review of ...
PURPOSE Idiopathic focal epilepsies in childhood including benign childhood epilepsy with occipital paroxysms (BEOP) or benign childhood epilepsy with centro-temporal spikes (BCECTS) are characterized by specific focal electrographic patterns as the name indicates. Generalized spike-wave discharges in children with idiopathic focal epilepsy can suggest a neurobiological continuum with the idiop...
Electroencephalography (EEG) is essential for the diagnosis of epilepsy, but it requires expertise and experience to identify abnormalities. It thus crucial develop automated models detection abnormalities in EEGs related epilepsy. This paper describes development a novel class compact convolutional neural networks (CNNs) detecting abnormal patterns electrodes The designed model inspired by CNN...
Mitochondrial disease is phenotypically and genetically heterogeneous with an estimated prevalence of 1 in 4,300. Mutations in the POLG gene, encoding the catalytic subunit of DNA polymerase gamma, are an important cause of mitochondrial disease. The spectrum of clinical manifestations in POLG-related mitochondrial disease is variable, with disease onset ranging from adulthood-onset dominant or...
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