نتایج جستجو برای: early infantile epileptic encephalopathy

تعداد نتایج: 725871  

Journal: :Annals of Clinical and Translational Neurology 2019

Journal: :Pediatric neurology 2006
Christian M Korff Douglas R Nordli

An increasing number of infantile epilepsy syndromes have been recognized. However, a significant number of infants (children aged 1-24 months) do not fit in any of the currently used subcategories. This article reviews the clinical presentation, electroencephalographic findings, evolution, and management of the following entities: early infantile epileptic encephalopathy, early myoclonic epile...

Journal: :Seizure 1995
P. S. Baxter D. Gardner-Medwin D. D. Barwick P. Ince J. Livingston D. Murdoch-Eaton

Seizures in a term infant with Ohtahara syndrome, associated with polymicrogyria, and a pre-term neonate with similar clinical features, failed to respond to conventional anticonvulsants, but were controlled with vigabatrin monotherapy. Another infant with Aicardi syndrome improved with vigabatrin. Autopsy in the first infant showed no evidence of intramyelinic oedema. The developmental outcome...

Journal: :AJNR. American journal of neuroradiology 1988
A L Thrush G D Marano

The CT and angiographic diagnosis and successful surgical treatment of a ruptured cerebral aneurysm in a 1-month-old girl are described. The incidence of intracranial aneurysms in infancy is less than 1 % [1] . A review of intracranial aneurysms in the neonate and infant is presented to define clearly the incidence and clinical characteristics of aneurysms in this age group. We have reviewed 43...

2016
Apostolos Papandreou Amy McTague Natalie Trump Gautam Ambegaonkar Adeline Ngoh Esther Meyer Richard H Scott Manju A Kurian

The gamma-aminobutyric acid type A receptor β3 gene (GABRB3) encodes the β3-subunit of the gamma-aminobutyric acid type A (GABAA ) receptor, which mediates inhibitory signalling within the central nervous system. Recently, GABRB3 mutations have been identified in a few patients with infantile spasms and Lennox-Gastaut syndrome. We report the clinical and electrographic features of a novel case ...

Journal: :Annals of Clinical and Translational Neurology 2019

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