《国际神经病学神经外科学杂志》.2004年.第8期
- Unusual differential diagnosis of leptomeningeal enhancement: moyamoya disease
- Positive and negative cerebral symptoms: the roles of Russell Reynolds and Hughlings Jackson
- William John Adie(1886–1935)
- ABN abstracts
- Features of the Sinushunt? and its influence on the cerebrospinal fluid system
- Self injurious behaviour in Tourette syndrome: correlates with impulsivity and impulse control
- Magnetic resonance spectroscopic determination of a neuronal and axonal marker in white matter predicts reversibility of deficits in seconda
- Recommended diagnostic criteria for paraneoplastic neurological syndromes
- Population based study of late onset cerebellar ataxia in south east Wales
- Two families with autosomal dominant progressive external ophthalmoplegia
- Disorders of body image
- Quick cognitive screening for clinicians. Mini mental, clock drawing and other brief tests
- Neurologic emergencies. A symptom orientated approach, 2nd edn
- Behavioral neurology & neuropsychology, 2nd edn
- Neuroscience at a glance, 2nd edn
- Genetic heterogeneity in ten families with myoclonus-dystonia
- Axonal degeneration and inflammation in acute optic neuritis
- Psychological characteristics of patients with newly developed psychogenic seizures
- Repetitive transcranial magnetic stimulation is as effective as fluoxetine in the treatment of depression in patients with Parkinson’s disea
- Octapeptide repeat insertions in the prion protein gene and early onset dementia
- Subacute dementia and imaging correlates in a case of Fahr’s disease
- Profiles of brain magnetic activity during a memory task in patients with Alzheimer’s disease and in non-demented elderly subjects, with or
- Is the common carotid artery intima–media thickness associated with functional outcome after acute ischaemic stroke?
- Dissection of the brain supplying arteries over the life span
- Raised intracranial pressure presenting with spontaneous periorbital bruising: two case reports
- Magnetic resonance imaging abnormalities with septic encephalopathy
- Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect
- Psychosocial outcomes at 18 months after good neurological recovery from aneurysmal subarachnoid haemorrhage
- Neuropsychological profile of young adults with spina bifida with or without hydrocephalus
- Increased intrathecal inflammatory activity in frontotemporal dementia: pathophysiological implications
- Increased intrathecal inflammatory activity in frontotemporal dementia: pathophysiological implications
- Premorbid cognitive testing predicts the onset of dementia and Alzheimer’s disease better than and independently of APOE genotype
- Dietary niacin and the risk of incident Alzheimer’s disease and of cognitive decline
- Cortical reorganisation in patients with MS
- Recommended diagnostic criteria for paraneoplastic neurological syndromes
- Mild cognitive impairment: aging to Alzheimer’s disease
- The Oxford dictionary of medical quotations
- Assessing tremor reduction and quality of life following thalamic deep brain stimulation for the treatment of tremor in multiple sclerosis
- Mesodiencephalic targeting of stimulating electrodes in patients with tremor caused by multiple sclerosis
- Outcome of contemporary surgery for chronic subdural haematoma: evidence based review
- Effect of a multidisciplinary clinic on survival in amyotrophic lateral sclerosis
- Transition from paediatric to adult neurological services
- Cessation of migraine following central retinal vein occlusion
- Five year follow up of a patient with spinal and bulbar muscular atrophy treated with leuprorelin
- Early symptoms of brain tumours
- No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation
- Combination of thalamic Vim stimulation and GPi pallidotomy synergistically abolishes Holmes’ tremor
- A case of acute urinary retention caused by periaqueductal grey lesion
- Disruption of facial affect processing in word deafness
- White matter abnormalities on MRI in neuroacanthocytosis
- Misdiagnosis of seizures: insulinoma presenting as adult-onset seizure disorder