From The Archives
Mitochondria and cortical gamma oscillations : food for thought?
Pathological network activity in Parkinson's disease : from neural activity and connectivity to causality?
Brain microbleeds and Alzheimer’s disease : innocent observation or key player?
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 : function, structure and behaviour in patients with left hemisphere damage
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 : a microdialysis study
Cerebral extracellular chemistry and outcome following traumatic brain injury : a microdialysis study of 223 patients
Adaptation of motor function after spinal cord injury : novel insights into spinal shock
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 : relevance to multiple sclerosis pathogenesis
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 : clinician, investigator, editor and leader—a retrospective appreciation
Why was the English Malady ‘English’?