Meanings of focal epilepsy in English

Conclusions: Propagation occurs often in patients with focal epilepsy, evaluated for surgery.

We observed that genetic generalized epilepsy and non-acquired focal epilepsy formed disease modules.

Childhood epilepsy with occipital paroxysms is an age-related idiopathic focal epilepsy.

Results: Several second-generation AEDs are effective for new-onset focal epilepsy.

Our results indicate that elders with focal epilepsy should be searched for vascular lesions.

European ancestry-derived PRS did not predict generalized epilepsy or focal epilepsy in Japanese-ancestry individuals.

Objective: To demonstrate progressive cortical thinning in patients with focal epilepsy distinct from cortical thinning associated with normal aging.

Conclusions and relevance: Widespread progressive cortical thinning exceeding that seen with normal aging may occur in patients with focal epilepsy.

Methods: Twelve patients with intractable focal epilepsy, in which NMAs were identified by electrical cortical stimulation, were enrolled in this study.

Small ADNFLE pedigrees with DEPDC5 mutations might actually represent a part of the broader familial focal epilepsy with variable foci phenotype.

Objective: To evaluate the effect of surgery on subjective and objective measures of sleep quality among patients with medically refractory focal epilepsy.

Objective: For patients with medically intractable focal epilepsy, the benefit of epilepsy surgery must be weighed against the risk of cognitive decline.

Signal analysis biomarkers, in an intra-operative setting, may be complementary tools to guide and tailor the resection in drug-resistant focal epilepsy patients.

All investigated epilepsy types, including lesional focal epilepsy patients, showed an increase in CNV burden in at least one tested category compared to controls.

Thirty-five ADHD children, 17 with focal epilepsy, one with generalised epilepsy, and 17 with no seizure disorder were evaluated.

Genome-wide CNV breakpoint association showed not only significant loci for genetic generalized and developmental and epileptic encephalopathy patients but also for lesional focal epilepsy patients.