From The Archives
Calcium dysregulation in Parkinson’s disease
The genetics of dystonia
Secondary and primary dystonia
Defective cerebellar control of cortical plasticity in writer’s cramp
Storage of a naturally acquired conditioned response is impaired in patients with cerebellar degeneration
Parkinson’s disease is associated with altered expression of CaV1 channels and calcium-binding proteins
Nigral stimulation for resistant axial motor impairment in Parkinson’s disease? A randomized controlled trial
Relation of lead trajectory and electrode position to neuropsychological outcomes of subthalamic neurostimulation in Parkinson’s disease
The coeruleus/subcoeruleus complex in rapid eye movement sleep behaviour disorders in Parkinson’s disease
Boosting chaperone-mediated autophagy in vivo mitigates α-synuclein-induced neurodegeneration
Progressive sleep and electroencephalogram changes in mice carrying the Huntington’s disease mutation
Longitudinal analysis of the electroencephalogram and sleep phenotype in the R6/2 mouse model of Huntington’s disease
Beclin 1 mitigates motor and neuropathological deficits in genetic mouse models of Machado–Joseph disease
Non-dystrophic myotonia
Lack of reliable evidence for a distinctive ε4−related cognitive phenotype that is independent from clinical diagnostic status
Amyloid tracers detect multiple binding sites in Alzheimer’s disease brain tissue
In vivo radioligand binding to translocator protein correlates with severity of Alzheimer’s disease
In vivo characterization of the early states of the amyloid-beta network
Diffusion tensor magnetic resonance imaging for single subject diagnosis in neurodegenerative diseases
Epigenetic induction of the Ink4a/Arf locus prevents Schwann cell overproliferation during nerve regeneration and after tumorigenic challenge
Axonal neuregulin 1 is a rate limiting but not essential factor for nerve remyelination
Tobacco smoking and disability progression in multiple sclerosis
Sodium accumulation is associated with disability and a progressive course in multiple sclerosis
Hallucinations of musical notation
What passes for reality
Czech family confirms the link between FBLN5 and Charcot–Marie–Tooth type 1 neuropathy
Radioactive in situ hybridization for Epstein–Barr virus–encoded small RNA supports presence of Epstein–Barr virus in the multiple sclerosis brain
Levodopa increases functional connectivity in the cerebellum and brainstem in Parkinson’s disease
Sensorineural hearing loss in OPA1-linked disorders
MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12
Microcystic macular degeneration from optic neuropathy