Developmental and epileptic encephalopathies (DEEs) are a heterogeneous group of
disorders characterized by early-onset, often severe epileptic seizures and EEG …

Since its first clinical description (on his son) by William James West (1793–1848) in 1841,
and the definition of the classical triad of (1) infantile spasms;(2) hypsarrhythmia, and (3) …

В руководстве представлены результаты 60-летней работы автора в области детской
и взрослой неврологии и эпилептологии. Впервые эпилептология представлена в …

Children with infantile spasms are likely to have a poor outcome. Outcome measures for
infantile spasms include primary response to treatment, relapse of spasms, neurological …

Objective The severe epilepsies of infancy (SEI) are a devastating group of disorders that
pose a major care and economic burden on society; early diagnosis is critical for optimal …

West syndrome (WS), also known as infantile spasms, occurs in infancy with a peak
between 4 and 7 months. Spasms, neurodevelopmental regression and hypsarrhythmia on …

ABSTRACT Introduction Focal cortical dysplasias (FCDs) represent the most common
etiology in pediatric drug-resistant focal epilepsies undergoing surgical treatment. The …

Summary Objective The multicenter National Infantile Spasms Consortium prospective
cohort was used to compare outcomes and phenotypic features of patients with infantile …

West syndrome, or infantile spasms syndrome is a frequently catastrophic infantile epileptic
encephalopathy with a variety of etiologies. Despite the heterogeneous nature of causes of …

Objective To investigate the diagnostic utility of high frequency oscillations (HFOs) via scalp
electroencephalogram (EEG) in infantile spasms. Methods We retrospectively analyzed …