Purpose: In severe myoclonic epilepsy of infancy (SME), multiple drug‐resistant focal and
generalized seizure types occur. Lamotrigine (LTG), found effective in many generalized and …

Background Duchenne muscular dystrophy (DMD) is a severe, progressive, and rare
neuromuscular, X-linked recessive disease. Dystrophin deficiency is the underlying cause of …

Malignant migrating partial seizures of infancy (MMPSI) is a rare epileptic encephalopathy
of infancy that combines pharmacoresistant seizures with developmental delay 1 . We …

Background Although several disease-modifying treatments are available for relapsing multiple
sclerosis, treatment effects have been more modest in progressive multiple sclerosis and …

Delta-brush is the dominant pattern of rapid oscillatory activity (8–25 Hz) in the human
cortex during the third trimester of gestation. Here, we studied the relationship between delta-…

Developing cortex generates endogenous activity that modulates the formation of functional
units, but how this activity is altered to support mature function is poorly understood. Using …

Mutations in the X‐linked cyclin‐dependent kinase‐like 5 (CDKL5) gene are responsible for
a severe encephalopathy with early epilepsy. So far, the electroclinical phenotype remains …

Due to its localization and function, the cornea is regularly exposed to sunlight and atmospheric
oxygen, mainly dioxygen, which produce reactive oxygen species (ROS). Therefore, …

Mutations in PCDH19, encoding protocadherin 19 on chromosome X, cause familial epilepsy
and mental retardation limited to females or Dravet‐like syndrome. Heterozygous females …

Abstract Spaces of Lorentz type called Orlicz‐Lorentz spaces are studied. There are given
necessary and sufficient conditions for the spaces to be order continuous, separable, KB‐…