When brawn benefits brain
New hope for the treatment of epilepsy
Can levodopa-induced dyskinesias go beyond the motor circuit?
Alterations in structural connectivity may contribute both to the occurrence of tics in Gilles de la Tourette syndrome and to their subsequent control
Pathophysiological concepts in the congenital myopathies
Physical activity and risk of Parkinson’s disease in the Swedish National March Cohort
Exome sequencing in undiagnosed inherited and sporadic ataxias
Adult-onset genetic leukoencephalopathies
Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2
Significance of neurovascular contact in classical trigeminal neuralgia
Transplantation of cerebellar neural stem cells improves motor coordination and neuropathology in Machado-Joseph disease mice
Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model
Predicting novel histopathological microlesions in human epileptic brain through transcriptional clustering
Targeting pharmacoresistant epilepsy and epileptogenesis with a dual-purpose antiepileptic drug
Tract-based spatial statistics to assess the neuroprotective effect of early erythropoietin on white matter development in preterm infants
Pivotal role of choline metabolites in remyelination
A network centred on the inferior frontal cortex is critically involved in levodopa-induced dyskinesias
Improving ideomotor limb apraxia by electrical stimulation of the left posterior parietal cortex
Genetic manipulation of adult-born hippocampal neurons rescues memory in a mouse model of Alzheimer’s disease
Why do patients with neurodegenerative frontal syndrome fail to answer
Altered structural connectivity of cortico-striato-pallido-thalamic networks in Gilles de la Tourette syndrome
Evidence for inhibitory deficits in the prefrontal cortex in schizophrenia
The perplexing conundrum of frontotemporal dementia
From Nissl stains to modern concepts of brainstem function
Does dominant pedunculopontine nucleus exist?
Age-dependent penetrance among females with X-linked adrenoleukodystrophy
TUBB4A novel mutation reinforces the genotype–phenotype correlation of hypomyelination with atrophy of the basal ganglia and cerebellum