The epilepsies are a heterogeneous group of disorders with many causes. However, a genetic aetiology may be present in up to 40 % of patients, and this proportion is even higher in epilepsy of childhood onset.1 The past decade has seen spectacular ad-vances in our understanding of the genetics of epilepsy at a molecular level, and several comprehensive reviews are available.2 3 It is apparent that epilepsy genes fall into several quite distinct classes including those in which mutations cause abnormal brain development, progressive neurodegeneration, disturbed en-ergy metabolism, or dysfunction of ion channels. The discovery that several idiopathic mendelia
Human hereditary epilepsy has been found related to ion channel mutations in voltage-gated channels ...
Many cases of pediatric epilepsy have a genetic component. For exam-ple, several twin studies have s...
Copyright © 2007 The American Society for Experimental NeuroTherapeutics, Inc. Published by Elsevier...
Genetic epilepsies are classified according to the mechanism of inheritance in three major groups: 1...
The identification of the first genes associated with idiopathic epilepsy has been an important brea...
To discuss some of the clinical and molecular genetic aspects of new discoveries in the field of the...
Genetic factors are now recognised to have an even more important role in epilepsies than previously...
Recent advances in molecular genetics led to the discovery of several genes for childhood epileptic ...
Epilepsy is a disorder of intermittent aberrant oscil-lations in cortical networks present in nearly...
The group of idiopathic epilepsies encompasses numerous syndromes without known organic substrate. G...
The genetic component of epilepsy has been known for over two millennia. The most commonly reported ...
Recent studies of the genetics of the epilepsies have identified surprising mechanisms and novel pat...
Background: Childhood epilepsies are caused by heterogeneous underlying disorders where approximat...
Epilepsy is a serious disorder of the central nervous system characterized by recurrent seizures. Th...
Understanding the aetiology of epilepsy is essential both for clinical management of patients and fo...
Human hereditary epilepsy has been found related to ion channel mutations in voltage-gated channels ...
Many cases of pediatric epilepsy have a genetic component. For exam-ple, several twin studies have s...
Copyright © 2007 The American Society for Experimental NeuroTherapeutics, Inc. Published by Elsevier...
Genetic epilepsies are classified according to the mechanism of inheritance in three major groups: 1...
The identification of the first genes associated with idiopathic epilepsy has been an important brea...
To discuss some of the clinical and molecular genetic aspects of new discoveries in the field of the...
Genetic factors are now recognised to have an even more important role in epilepsies than previously...
Recent advances in molecular genetics led to the discovery of several genes for childhood epileptic ...
Epilepsy is a disorder of intermittent aberrant oscil-lations in cortical networks present in nearly...
The group of idiopathic epilepsies encompasses numerous syndromes without known organic substrate. G...
The genetic component of epilepsy has been known for over two millennia. The most commonly reported ...
Recent studies of the genetics of the epilepsies have identified surprising mechanisms and novel pat...
Background: Childhood epilepsies are caused by heterogeneous underlying disorders where approximat...
Epilepsy is a serious disorder of the central nervous system characterized by recurrent seizures. Th...
Understanding the aetiology of epilepsy is essential both for clinical management of patients and fo...
Human hereditary epilepsy has been found related to ion channel mutations in voltage-gated channels ...
Many cases of pediatric epilepsy have a genetic component. For exam-ple, several twin studies have s...
Copyright © 2007 The American Society for Experimental NeuroTherapeutics, Inc. Published by Elsevier...