From The Archives
Mitochondria and cortical gamma oscillations
Pathological network activity in Parkinson's disease
Brain microbleeds and Alzheimer’s disease
Gamma oscillations in the hippocampus require high complex I gene expression and strong functional performance of mitochondria
Resting oscillatory cortico-subthalamic connectivity in patients with Parkinson’s disease
Inhibition of phosphodiesterases rescues striatal long-term depression and reduces levodopa-induced dyskinesia
The long-term risk of premature mortality in people with epilepsy
Foetal antiepileptic drug exposure and verbal versus non-verbal abilities at three years of age
What is the role of the uncinate fasciculus? Surgical removal and proper name retrieval
Left inferior frontal cortex and syntax
Predicting functional decline in behavioural variant frontotemporal dementia
White matter damage and cognitive impairment after traumatic brain injury
In vivo monitoring of neuronal loss in traumatic brain injury
Cerebral extracellular chemistry and outcome following traumatic brain injury
Adaptation of motor function after spinal cord injury
Phosphatase and tensin homologue/protein kinase B pathway linked to motor neuron survival in human superoxide dismutase 1-related amyotrophic lateral sclerosis
Primary retinal pathology in multiple sclerosis as detected by optical coherence tomography
Related B cell clones populate the meninges and parenchyma of patients with multiple sclerosis
CD161highCD8+T cells bear pathogenetic potential in multiple sclerosis
Adenosine triphosphate-binding cassette transporters mediate chemokine (C-C motif) ligand 2 secretion from reactive astrocytes
Acid-sensing ion channel 1 is involved in both axonal injury and demyelination in multiple sclerosis and its animal model
Nav1.8 channelopathy in mutant mice deficient for myelin protein zero is detrimental to motor axons
A mutation in the RNF170 gene causes autosomal dominant sensory ataxia
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene
Professor P. K. Thomas
Why was the English Malady ‘English’?