Editorial
The neural basis of morality
‘That DAT’ gene that causes dystonia-parkinsonism
Is PTEN hyperactivity behind poor regeneration in diabetic neuropathy?
Consulting the vestibular system is simply a must if you want to optimize gaze shifts
Inability to empathize
NaV1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery
Episodic ataxia type 1
Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
Diagnostic serum glycosylation profile in patients with intellectual disability as a result of MAN1B1 deficiency
Enhanced excitability of MRGPRA3- and MRGPRD-positive nociceptors in a model of inflammatory itch and pain
Regeneration of diabetic axons is enhanced by selective knockdown of the PTEN gene
Characterization of ocular motor deficits in congenital facial weakness
Vestibular and cerebellar contribution to gaze optimality
White matter development in children with benign childhood epilepsy with centro-temporal spikes
Dopamine transporter deficiency syndrome
Mild cognitive impairment is linked with faster rate of cortical thinning in patients with Parkinson’s disease longitudinally
Resting state functional MRI in Parkinson’s disease
Selective serotonin reuptake inhibition modulates response inhibition in Parkinson’s disease
A bimodal neurophysiological study of motor control in attention-deficit hyperactivity disorder
Compensatory mechanisms in higher-educated subjects with Alzheimer’s disease
Asymmetry and heterogeneity of Alzheimer’s and frontotemporal pathology in primary progressive aphasia
Differential reorganization of three syntax-related networks induced by a left frontal glioma
Arousal responses to noxious stimuli in somatoparaphrenia and anosognosia
Evidence for both compensatory plastic and disuse atrophy-related neuroanatomical changes in the blind
Right anterior temporal lobe dysfunction underlies theory of mind impairments in semantic dementia
Arrested development
Sad psychosurgery
From The Archives
Corrigendum
A single strand that links multiple neuropathologies in human disease
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The corpus callosum of Albert Einstein‘s brain
A rare anatomical variation newly identifies the brains of C.F. Gauss and C.H. Fuchs in a collection at the University of Göttingen
Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain
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Spontaneous versus deliberate vicarious representations
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