File Name: epileptic syndromes in infancy childhood and adolescence .zip
Metrics details. In this paper, seizure types, and epilepsy syndromes are elucidated as per ILAE classification.
This 6th edition reviews some of the most noteworthy developments in the field, particularly in epileptic syndromes, but also focuses on the genetic aspects of the syndromes and their development. Progress brought about by advances in neuroimaging is also discussed in addition to specific etiologies such as parasitic diseases and immune and autoimmune diseases. This book written by the current leading specialists is recognized worldwide as the international reference in epilepsy. The syndromic approach of epilepsies : Classifications, epidemiology, prognosis - Genetic bases of epileptic syndromes - Animal models of epileptic syndromes - EEG traits of epileptic syndromes - Neuroimaging and epileptic syndromes - Drug development in epileptic syndromes. Syndromes in childhood and adolescence : Lennox-Gastaut syndrome - Idiopathic focal epilepsies in childhood - Encephalopathy with status epilepticus during slow sleep ESES including Landau-Kleffner syndrome - Absence epilepsies: CAE, JAE, early absences, myoclonic absences and other syndromes - Isolated focal seizures in adolescence - Juvenile myoclonic epilepsies.
Skip to search form Skip to main content You are currently offline. Some features of the site may not work correctly. DOI: Nabbout and O. Nabbout , O.
The outcome measure was death. Standardized mortality ratios were used to quantify the excess mortality in the cohort relative to the population. Ten deaths were associated with the underlying cause of the seizures, 2 were associated with the occurrence or probable occurrence of seizures, and 1 was unrelated to seizures or the underlying disorder. On multivariable analysis, symptomatic etiology rate ratio, The overall standardized mortality ratio for the cohort was 7. In children with symptomatic epilepsy, the standardized mortality ratio was
Several specific epileptic syndromes begin during adolescence, including juvenile myoclonic epilepsy, juvenile absence epilepsy, epilepsy with tonic-clonic seizures on awakening, and some forms of partial epilepsies. These syndromes need careful attention in terms of drug treatment because adolescence is a complex period socially and behaviourally and the adverse effects of drugs during this period could prove problematic. Whether all epilepsies that begin during adolescence require treatment is a difficult issue. Furthermore, the avoidance of precipitating factors could be a sufficient therapeutic strategy in some patients. Instructions should be given regarding the potentially seizure-triggering effect of certain behaviours, e. If drug treatment is required, the choice of drug will depend on the identified epileptic syndrome and the efficacy and adverse effect profile of the drug.
Она в конце концов перестала протестовать, но это продолжало ее беспокоить. Я зарабатываю гораздо больше, чем в состоянии потратить, - думала она, - поэтому будет вполне естественным, если я буду платить. Но если не считать его изрядно устаревших представлений о рыцарстве, Дэвид, по мнению Сьюзан, вполне соответствовал образцу идеального мужчины.
Шифр не поддается взлому, - сказал он безучастно. Не поддается. Сьюзан не могла поверить, что это сказал человек, двадцать семь лет работавший с шифрами.
Кто тебе сказал про вирус.