From The Archives
Dysfunctional mitochondrial maintenance
Assembly factors as a new class of disease genes for mitochondrial complex I deficiency
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy ‘plus’ phenotype
Downregulation of apoptosis-inducing factor in Harlequin mice induces progressive and severe optic atrophy which is durably prevented by AAV2-AIF1 gene therapy
Increased capillaries in mitochondrial myopathy
Sensory neuronopathy in patients harbouring recessive polymerase γ mutations
A rat model of Charcot–Marie–Tooth disease 1A recapitulates disease variability and supplies biomarkers of axonal loss in patients
Colony-stimulating factor-1 mediates macrophage-related neural damage in a model for Charcot–Marie–Tooth disease type 1X
Defective dentate nucleus GABA receptors in essential tremor
Believing is perceiving
Dopaminergic neuroprotection of hormonal replacement therapy in young and aged menopausal rats
Subthalamic nucleus stimulation reverses spinal motoneuron activity in parkinsonian patients
Alpha oscillations in the pedunculopontine nucleus correlate with gait performance in parkinsonism
Severe olfactory dysfunction is a prodromal symptom of dementia associated with Parkinson's disease
Alzheimer's disease pattern of brain atrophy predicts cognitive decline in Parkinson's disease
Blood–brain barrier P-glycoprotein function in Alzheimer's disease
Impairments of auditory scene analysis in Alzheimer's disease
Executive deficits are related to the inferior frontal junction in early dementia
Effect of growth hormone deficiency on brain structure, motor function and cognition
Theory of mind impairments in patients with semantic dementia
Semantic memory is impaired in patients with unilateral anterior temporal lobe resection for temporal lobe epilepsy
Spreading convulsions, spreading depolarization and epileptogenesis in human cerebral cortex
Cortical activation changes underlying stimulation-induced behavioural gains in chronic stroke
The discovery of the pyramidal neurons
A comment on impaired peri-nidal cerebrovascular reserve in seizure patients with brain arteriovenous malformations
Mutations of TSEN and CASK genes are prevalent in pontocerebellar hypoplasias type 2 and 4
Cerebral microbleeds in familial Alzheimer’s disease
The impact of dementia prevalence on the utility of the AD8