Model of autism: increased ratio of excitation/inhibition in key neural systems

JLR Rubenstein, MM Merzenich - Genes, Brain and Behavior, 2003 - Wiley Online Library
Autism is a severe neurobehavioral syndrome, arising largely as an inherited disorder,
which can arise from several diseases. Despite recent advances in identifying some genes …

The neurobiology of antiepileptic drugs

MA Rogawski, W Löscher - Nature reviews neuroscience, 2004 - nature.com
Antiepileptic drugs (AEDs) provide satisfactory control of seizures for most patients with
epilepsy. The drugs have the remarkable ability to protect against seizures while permitting …

Mechanisms of epileptogenesis: a convergence on neural circuit dysfunction

EM Goldberg, DA Coulter - Nature Reviews Neuroscience, 2013 - nature.com
Epilepsy is a prevalent neurological disorder associated with significant morbidity and
mortality, but the only available drug therapies target its symptoms rather than the underlying …

Ion channels in genetic epilepsy: from genes and mechanisms to disease-targeted therapies

J Oyrer, S Maljevic, IE Scheffer, SF Berkovic… - Pharmacological …, 2018 - Elsevier
Epilepsy is a common and serious neurologic disease with a strong genetic component.
Genetic studies have identified an increasing collection of disease-causing genes. The …

Epilepsy in children

R Guerrini - The Lancet, 2006 - thelancet.com
Summary 10· 5 million children worldwide are estimated to have active epilepsy. Over the
past 15 years, syndrome-oriented clinical and EEG diagnosis, and better aetiological …

Nicotinic acetylcholine receptors: from structure to brain function

RC Hogg, M Raggenbass, D Bertrand - Reviews of physiology …, 2003 - Springer
Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels and can be
divided into two groups: muscle receptors, which are found at the skeletal neuromuscular …

The hidden genetics of epilepsy—a clinically important new paradigm

RH Thomas, SF Berkovic - Nature Reviews Neurology, 2014 - nature.com
Understanding the aetiology of epilepsy is essential both for clinical management of patients
and for conducting neurobiological research that will direct future therapies. The aetiology of …

Sodium channel SCN1A and epilepsy: Mutations and mechanisms

A Escayg, AL Goldin - Epilepsia, 2010 - Wiley Online Library
Mutations in a number of genes encoding voltage‐gated sodium channels cause a variety of
epilepsy syndromes in humans, including genetic (generalized) epilepsy with febrile …

Severe myoclonic epilepsy in infancy (Dravet syndrome)

C Dravet, M Bureau, H Oguni… - … syndromes in infancy …, 2005 - books.google.com
According to the 1989 revised classification of the Interna-tional League Against Epilepsy,
this syndrome is charac-terized by febrile and afebrile generalized and unilateral clonic or …

[HTML][HTML] Genetic variations in GABA metabolism and epilepsy

Y Feng, ZH Wei, C Liu, GY Li, XZ Qiao, YJ Gan… - … : European Journal of …, 2022 - Elsevier
Epilepsy is a paroxysmal brain disorder that results from an imbalance between neuronal
excitation and inhibition. Gamma-aminobutyric acid (GABA) is the most important inhibitory …