From The Archives
Defining and treating leucine-rich glioma inactivated 1 antibody associated autoimmunity
Off to never-never land
Beyond taxol
White matter structural connectivity underlying semantic processing
Impairment only on the fluency subtest of the Frontal Assessment Battery after prefrontal lesions
Anterior temporal lobe degeneration produces widespread network-driven dysfunction
The orbitofrontal cortex is involved in emotional enhancement of memory
Alterations in α4β2 nicotinic receptors in cognitive decline in Alzheimer’s aetiopathology
DNA methylation map of mouse and human brain identifies target genes in Alzheimer’s disease
Correlation of dopaminergic terminal dysfunction and microstructural abnormalities of the basal ganglia and the olfactory tract in Parkinson’s disease
Ursocholanic acid rescues mitochondrial function in common forms of familial Parkinson’s disease
Purkinje cell axonal anatomy
Phase dependent modulation of tremor amplitude in essential tremor through thalamic stimulation
Can we still dream when the mind is blank? Sleep and dream mentations in auto-activation deficit
Genotype-phenotype correlations in hyperekplexia
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies
Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
Faciobrachial dystonic seizures
Asymmetry of planum temporale constrains interhemispheric language plasticity in children with focal epilepsy
The value of magnetoencephalography for seizure-onset zone localization in magnetic resonance imaging-negative partial epilepsy
The lifelong course of chronic epilepsy
The reel of consciousness
Ocular paradoxical movement and severity of Parkinson’s disease
The cuneiform nucleus may be involved in the regulation of skeletal muscle tone by motor pathway
Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy