From The Archives
How Dravet syndrome became a model for studying childhood genetic epilepsies
Is the migrainous female brain different? Some new evidence
The outcome of therapies in refractory and super-refractory convulsive status epilepticus and recommendations for therapy
Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome
Blurring in patients with temporal lobe epilepsy
Structural substrates for resting network disruption in temporal lobe epilepsy
Fluoxetine restores spatial learning but not accelerated forgetting in mesial temporal lobe epilepsy
Fluoxetine inhibits matrix metalloprotease activation and prevents disruption of blood–spinal cord barrier after spinal cord injury
Effect of analgesics and sedatives on the occurrence of spreading depolarizations accompanying acute brain injury
Complexity of intracranial pressure correlates with outcome after traumatic brain injury
Familial aggregation of congenital hydrocephalus in a nationwide cohort
Diencephalic–mesencephalic junction dysplasia
Calpastatin-mediated inhibition of calpains in the mouse brain prevents mutant ataxin 3 proteolysis, nuclear localization and aggregation, relieving Machado–Joseph disease
The neurobiology of glucocerebrosidase-associated parkinsonism
The catechol-O-methyltransferase Val158Met polymorphism modulates fronto-cortical dopamine turnover in early Parkinson’s disease
Imaging and acetylcholinesterase inhibitor response in dementia with Lewy bodies
The effects of the dopamine agonist rotigotine on hemispatial neglect following stroke
No inherent left and right side in human ‘mental number line’
A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations
Is misery perfusion still a predictor of stroke in symptomatic major cerebral artery disease?
The PREP algorithm predicts potential for upper limb recovery after stroke
Assessing the risk of central post-stroke pain of thalamic origin by lesion mapping
Her versus his migraine
The migraine theories of Liveing and Latham
A headache history
Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease
MFN2 mutations cause compensatory mitochondrial DNA proliferation
Quantitative evaluation of the human subventricular zone
MFN2, a new gene responsible for mitochondrial DNA depletion