The authors studied 10 patients aged between six and 23 years (mean age 14 years 5
months) with magnetic resonance imaging, which detected bilateral 'macrogyric�…

The authors describe the electroclinical aspects and evolution of nine cases of myoclonic
epileptic encephalopathy which began between two days and ten weeks of life. at onset it is�…

We describe a young man with a progressive neurological disorder including myoclonus,
mental retardation, muscle weakness and a mitochondrial myopathy (myoclonus epilepsy�…

Benign myoclonic epilepsy in infancy (BME) is characterized by the occurrence of brief
myoclonic attacks in normal infants aged 4 months to 3 years. There is no prior personal�…

In 17 epileptics receiving carbamazepine (CBZ) alone or in combination with other
anticonvulsant drugs, administration of triacetyloleandomycin (Tri A) led to an acute and�…

Purpose: We wished to study immune system dysfunction which has been proposed as a
potential cause of epilepsy. Epileptogenic action of antibodies directed against GM1�…

We retrospectively collected plasma level assessments performed in 96 adult patients with
epilepsy on stable monotherapy, including 9 patients on clobazam (CLB), 34 on�…

PURPOSE: To try to prove in patients with refractory symptomatic epilepsy due to early brain
injury involving thalamus and complicated by CSWS the effects of the isolation of the injured�…

Purpose: Gaucher disease, the inherited deficiency of the lysosomal enzyme
glucocerebrosidase, is characterized by genotypic and phenotypic heterogeneity. We�…

Although benign forms of epilepsies with onset in infancy have recently been recognized,
the occurrence of seizures in an infant or very young child is very often an event of great�…