Surgery for epilepsy
Surgery for epilepsy - West, S - 2019 | Cochrane Library Skip to Content Cookies Our site uses
cookies to improve your experience. You can find out more about our use of cookies in About …
cookies to improve your experience. You can find out more about our use of cookies in About …
Genetic landscape of common epilepsies: advancing towards precision in treatment
Epilepsy, a neurological disease characterized by recurrent seizures, is highly
heterogeneous in nature. Based on the prevalence, epilepsy is classified into two types …
heterogeneous in nature. Based on the prevalence, epilepsy is classified into two types …
The natural history of epilepsy: an epidemiological view
Better information of the natural history of epilepsy has important implications for
understanding the underlying neurobiology, evaluating treatment strategies, and planning …
understanding the underlying neurobiology, evaluating treatment strategies, and planning …
Phenobarbital for the treatment of epilepsy in the 21st century: a critical review
P Kwan, MJ Brodie - Epilepsia, 2004 - Wiley Online Library
Phenobarbital (PB) is the most widely used antiepileptic drug (AED) in the developing world
and remains a popular choice in many industrialized countries. Meta‐analyses of …
and remains a popular choice in many industrialized countries. Meta‐analyses of …
Fever, genes, and epilepsy
About 13% of patients with epilepsy have a history of febrile seizures (FS). Studies of familial
forms suggest a genetic component to the epidemiological link. Indeed, in certain …
forms suggest a genetic component to the epidemiological link. Indeed, in certain …
The prion protein knockout mouse: a phenotype under challenge
AD Steele, S Lindquist, A Aguzzi - Prion, 2007 - Taylor & Francis
The key pathogenic event in prion disease involves misfolding and aggregation of the
cellular prion protein (PrP). Beyond this fundamental observation, the mechanism by which …
cellular prion protein (PrP). Beyond this fundamental observation, the mechanism by which …
Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases
Abnormal prion proteins are responsible for several fatal neurodegenerative diseases in
humans and in animals, including Creutzfeldt–Jakob disease (CJD), Gerstmann–Sträussler …
humans and in animals, including Creutzfeldt–Jakob disease (CJD), Gerstmann–Sträussler …
Genetic association studies in epilepsy:“the truth is out there”
NCK Tan, JC Mulley, SF Berkovic - Epilepsia, 2004 - Wiley Online Library
Success has been achieved in identifying many mutations in rare monogenic epilepsy
syndromes by using linkage analysis, but dissecting the genetic basis of common epilepsy …
syndromes by using linkage analysis, but dissecting the genetic basis of common epilepsy …
[HTML][HTML] Multi-omics in mesial temporal lobe epilepsy with hippocampal sclerosis: Clues into the underlying mechanisms leading to disease
Mesial temporal lobe epilepsy (MTLE) is one of the most common types of focal epilepsy in
the adult population. MTLE is frequently associated with a specific histopathological lesion …
the adult population. MTLE is frequently associated with a specific histopathological lesion …
MRI evidence of mesial temporal sclerosis in sporadic “benign” temporal lobe epilepsy
A Labate, P Ventura, A Gambardella, E Le Piane… - Neurology, 2006 - AAN Enterprises
Objective: To determine whether there is MRI-detectable mesial temporal sclerosis (MTS) in
patients with sporadic benign temporal lobe epilepsy (BTLE). Methods: Brain MRIs were …
patients with sporadic benign temporal lobe epilepsy (BTLE). Methods: Brain MRIs were …