Editorial
New hope for ameliorating stroke-induced deficits?
Neuromelanin-sensitive imaging in patients with idiopathic rapid eye movement sleep behaviour disorder
Amyloid biomarkers
Time in the orbitofrontal cortex
Is Huntington's disease a tauopathy?
Iron and dopamine
CCDC88A mutations cause PEHO-like syndrome in humans and mouse
Liver transplant in ethylmalonic encephalopathy
Inherited erythromelalgia due to mutations in SCN9A
Interictal spikes and epileptic seizures
Motor cortex and hippocampus are the two main cortical targets in LGI1-antibody encephalitis
Attenuated traumatic axonal injury and improved functional outcome after traumatic brain injury in mice lacking Sarm1
Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis
Therapeutic NOTCH3 cysteine correction in CADASIL using exon skipping
Longitudinal patterns of leukoaraiosis and brain atrophy in symptomatic small vessel disease
Electrical stimulation of the motor cortex enhances treatment outcome in post-stroke aphasia
White matter hyperintensities and imaging patterns of brain ageing in the general population
The coeruleus/subcoeruleus complex in idiopathic rapid eye movement sleep behaviour disorder
Electroencephalographic prodromal markers of dementia across conscious states in Parkinson’s disease
Tractography patterns of subthalamic nucleus deep brain stimulation
MRI visual rating scales in the diagnosis of dementia
Cerebrospinal fluid analysis detects cerebral amyloid-β accumulation earlier than positron emission tomography
Regulatory T cells delay disease progression in Alzheimer-like pathology
Early and protective microglial activation in Alzheimer’s disease
Eliminating microglia in Alzheimer’s mice prevents neuronal loss without modulating amyloid-β pathology
Neural substrates of vulnerability to postsurgical delirium as revealed by presurgical diffusion MRI
The neural dynamics of reward value and risk coding in the human orbitofrontal cortex
High prevalence of CHCHD10 mutation in patients with frontotemporal dementia from China
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The dorsal cingulate cortex as a critical gateway in the network supporting conscious awareness
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Nigrostriatal denervation sine parkinsonism
Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene
Corrigendum