Brain
(ISSN: 0006-8950, 1460-2156)
Show only: Full-text on Medscape
2009 - 132 (Pt 10)
- Balanced and responsible journalism.
- Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
- Sporadic Creutzfeldt-Jakob disease: discrete subtypes or a spectrum of disease?
- Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.
- Functional definition of seizure provides new insight into post-traumatic epileptogenesis.
- Oxaliplatin-induced neurotoxicity: changes in axonal excitability precede development of neuropathy.
- Symptoms 'unexplained by organic disease' in 1144 new neurology out-patients: how often does the diagnosis change at follow-up?
- Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.
- Increased risk and worse prognosis of myocardial infarction in patients with prior hospitalization for epilepsy--the Stockholm Heart Epidemiology Program.
- How the brain repairs stuttering.
- The human brain utilizes lactate via the tricarboxylic acid cycle: a 13C-labelled microdialysis and high-resolution nuclear magnetic resonance study.
- Making sense of progressive non-fluent aphasia: an analysis of conversational speech.
- Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.
- Expression of neurotrophic factors in diabetic muscle--relation to neuropathy and muscle strength.
- Abnormal sensorimotor plasticity in organic but not in psychogenic dystonia.
- Early plasticity versus early vulnerability: the problem of heterogeneous lesion types.
- Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.
- Frequency, prognosis and surgical treatment of structural abnormalities seen with magnetic resonance imaging in childhood epilepsy.
- Chronic temporal lobe epilepsy: a neurodevelopmental or progressively dementing disease?
- Impaired eye movements in post-concussion syndrome indicate suboptimal brain function beyond the influence of depression, malingering or intellectual ability.
- Symptoms and signs of syncope: a review of the link between physiology and clinical clues.
- Parkinson's disease, DBS and suicide: a role for serotonin?
- Speech experience shapes the speechreading network and subsequent deafness facilitates it.
- Differential phenotype in Parkinson's disease patients with severe versus mild GBA mutations.
- Imbalance of neural cell adhesion molecule and polysialyltransferase alleles causes defective brain connectivity.
- Brain regions underlying word finding difficulties in temporal lobe epilepsy.
- Disembodied hallucinatory voices: comment on Sommer et al., 2008 Brain 131, 3169-77.
- In the psychiatrist's chair: how neurologists understand conversion disorder.
- Thalamo-striatal diffusion reductions precede disease onset in prion mutation carriers.
- On the pathogenesis of collagen VI muscular dystrophies--comment on article of Hicks et al.
