From the Archives
Genetics of Parkinson's disease: LRRK2 on the rise
Kleine—Levin syndrome: a systematic review of 186 cases in the literature
PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data
Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22–p24
Periventricular nodular heterotopia with overlying polymicrogyria
Greater functional recovery after temporal lobe epilepsy surgery in children
Visual search improvement in hemianopic patients after audio-visual stimulation
Attentional responses to unattended stimuli in human parietal cortex
Right anterior superior temporal activation predicts auditory sentence comprehension following aphasic stroke
Does gender play a role in functional asymmetry of ventromedial prefrontal cortex?
Better without (lateral) frontal cortex? Insight problems solved by frontal patients
A longitudinal study of cognition in primary progressive multiple sclerosis
Role of return migration in the emergence of multiple sclerosis in the French West Indies
Magnetization transfer histograms in clinically isolated syndromes suggestive of multiple sclerosis
MTI of white matter hyperintensities
Evidence of reversible axonal dysfunction in systemic lupus erythematosus: a proton MRS study
Brain motor system function after chronic, complete spinal cord injury
Autologous olfactory ensheathing cell transplantation in human spinal cord injury
Olfactory ensheathing glial co-grafts improve functional recovery in rats with 6-OHDA lesions
Factors affecting the clinical outcome after neural transplantation in Parkinson's disease
Envenoming bites by kraits: the biological basis of treatment-resistant neuromuscular paralysis
Medicine and literature
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*
Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies—a comment