From The Archives
Defective N-linked protein glycosylation pathway in congenital myasthenic syndromes
Dystonia : hopes for a better diagnosis and a treatment with long-lasting effect
The cerebellum in Parkinson’s disease
Rhythm-specific modulation of the sensorimotor network in drug-naïve patients with Parkinson’s disease by levodopa
Evidence for adaptive cortical changes in swallowing in Parkinson’s disease
Visual exploration in Parkinson’s disease and Parkinson’s disease dementia
Parietal substrates for dimensional effects in visual search : evidence from lesion-symptom mapping
Bilateral pallidal stimulation in cervical dystonia : blinded evidence of benefit beyond 5 years
The functional neuroimaging correlates of psychogenic versus organic dystonia
Aristotle’s illusion reveals interdigit functional somatosensory alterations in focal hand dystonia
Distinct illusory own-body perceptions caused by damage to posterior insula and extrastriate cortex
Hippocampal CA1 deformity is related to symptom severity and antipsychotic dosage in schizophrenia
The stress model of chronic pain : evidence from basal cortisol and hippocampal structure and function in humans
Epigenetic transcriptional activation of monocyte chemotactic protein 3 contributes to long-lasting neuropathic pain
Diverging patterns of amyloid deposition and hypometabolism in clinical variants of probable Alzheimer’s disease
Motor cortex and gait in mild cognitive impairment : a magnetic resonance spectroscopy and volumetric imaging study
MEDNIK syndrome : a novel defect of copper metabolism treatable by zinc acetate therapy
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome
Oxidative stress regulates the ubiquitin–proteasome system and immunoproteasome functioning in a mouse model of X-adrenoleukodystrophy
Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6
GABA deficit in the visual cortex of patients with neurofibromatosis type 1 : genotype–phenotype correlations and functional impact
Co-induction of the heat shock response ameliorates disease progression in a mouse model of human spinal and bulbar muscular atrophy : implications for therapy
Congenital myasthenic syndromes due to mutations in ALG2 and ALG14
Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour
Magnetic flimmers : ‘light in the electromagnetic darkness’
Wit and wickedness : is it all in the brain?