Numerous numbers of pre-, peri-and postnatal damages cause West syndrome in early
infancy, however, etiology in many cases are not still elucidated despite intensive …

To provide up-to-date information on adrenocorticotropic hormone (ACTH) therapy in the
treatment of West syndrome, a review of the Finnish studies was made in answer to the …

Although corticotropin (ACTH) is still the most effective drug for the treatment of West
syndrome, a variety of other treatment modalities have been tried because of corticotropin's …

This study examines factors influencing the evolution of West syndrome to Lennox-Gastaut
syndrome. The study population comprised 98 patients diagnosed with West syndrome and …

Aim: To analyze the evolution of seizures, electroencephalographic (EEG) features, seizure
outcomes, and social outcomes, in order to formulate a basis for the long-term prognosis of …

On a database of the Japanese medical literature between 1970 and 2000, there were 29
patients with West syndrome showing spontaneous remission. In 25/29 (86%) of the …

Ictal electroencephalographic/video recordings of 42 patients with West syndrome (WS)
were reviewed to define the relation between ictal, clinical, and EEG features and etiology or …

The clinical and electroencephalographic data of 31 children with cryptogenic West
syndrome (WS), selected from a series of 103 WS patients, with a follow‐up between 4 and …

A subgroup of patients with West syndrome (WS) also have focal features, and some of
these patients respond to surgical intervention. To determine the incidence of focal features …