Editorial
From The Archives
Complication begets clarification in classification
Oligodendroglia
Sex, drugs and Parkinson’s disease
Parkinson's disease, insulin resistance and novel agents of neuroprotection
C9orf72 repeat expansions are a rare genetic cause of parkinsonism
Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohort
Neural response to visual sexual cues in dopamine treatment-linked hypersexuality in Parkinson’s disease
A progressive dopaminergic phenotype associated with neurotoxic conversion of α-synuclein in BAC-transgenic rats
Striatal allografts in patients with Huntington’s disease
Temporal expectation in focal hand dystonia
Corticospinal tract degeneration associated with TDP-43 type C pathology and semantic dementia
Oligodendrocyte dysfunction in the pathogenesis of amyotrophic lateral sclerosis
Degeneration of serotonergic neurons in amyotrophic lateral sclerosis
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity
Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies
A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3
Overlapping cortical malformations and mutations in TUBB2B and TUBA1A
Loss of SOX10 function contributes to the phenotype of human Merlin-null schwannoma cells
Integrin control of the transforming growth factor-β pathway in glioblastoma
CHOP regulates the p53–MDM2 axis and is required for neuronal survival after seizures
The adult seizure and social outcomes of children with partial complex seizures
Words and objects at the tip of the left temporal lobe in primary progressive aphasia
Damage to ventral and dorsal language pathways in acute aphasia
Phonological deficits in specific language impairment and developmental dyslexia
Functional magnetic resonance imaging of chronic dysarthric speech after childhood brain injury
Intracerebral haemorrhage profiles are changing
Single nucleotide polymorphisms associated with sporadic brain arteriovenous malformations
A landmark publication in movement disorders
Multisystem fatal infantile disease caused by a novel homozygous EARS2 mutation
Alcohol, sleepwalking and violence
Persistence of the treatment effect of idebenone in Leber’s hereditary optic neuropathy
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy