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© The Author (2008). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
© The Author (2009). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
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Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
Antagonism of the mammalian target of rapamycin selectively mediates metabolic effects of epidermal growth factor receptor inhibition and protects human malignant glioma cells from hypoxia-induced cell death
Ravel's last illness: a unifying hypothesis
Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle disease
Selective adenosine A2a receptor antagonism reduces JNK activation in oligodendrocytes after cerebral ischaemia
Effect of Alemtuzumab (CAMPATH 1-H) in patients with inclusion-body myositis
Can CBT substantially change grey matter volume in chronic fatigue syndrome?
Migraine headache is not associated with cerebral or meningeal vasodilatation—a 3T magnetic resonance angiography study
Defining Meyer's loop-temporal lobe resections, visual field deficits and diffusion tensor tractography
Reply to: can CBT substantially change grey matter volume in chronic fatigue syndrome?
Editorial
The muddle of embodiment
Bilateral widespread mechanical pain sensitivity in carpal tunnel syndrome: evidence of central processing in unilateral neuropathy
Polysialic acid glycomimetics promote myelination and functional recovery after peripheral nerve injury in mice
The neural basis of tool use
Functional compensation of motor function in pre-symptomatic Huntington's disease
Motor cortex stimulation for the treatment of refractory peripheral neuropathic pain
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5
Not on the face alone: perception of contextualized face expressions in Huntington's disease
Recovery from spinal cord injury: regeneration, plasticity and rehabilitation
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain
Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study
Evaluation and management of gliomas of the anterior visual pathways, by N. R. Miller, W. J. Iliff and W. R. Green (From the Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, MD, USA) Brain 1974: 97; 743-754; and The biological and clinical behaviour of pilocytic astrocytomas of the optic pathways, by Adam Borit and Edward P. Richardson Jr (From the CS Kubik Laboratory for Neuropathology of the Department of Pathology and the Neurology service of the Massachusetts General Hospital, the Howe Laboratory of Ophthalmology, Massachusetts Eye and Ear Infirmary, and the Departments of Neurology-Neuropathology, Ophthalmology and Pathology, Harvard Medical School, Boston, MA, USA) Brain 1982: 105; 161-187.
Recessive twinkle mutations cause severe epileptic encephalopathy
The effect of N-acetyl-aspartyl-glutamate and N-acetyl-aspartate on white matter oligodendrocytes
Prism adaptation reverses the local processing bias in patients with right temporo-parietal junction lesions
Reply to: Migraine headache is not associated with cerebral or meningeal vasodilatation—a 3T magnetic resonance angiography study
Sensory capacity of reinnervated skin after redirection of amputated upper limb nerves to the chest
Morphing voxels: the hype around structural imaging of headache patients
Subcortical damage and white matter disconnection associated with non-fluent speech
Differential effects of anti-Nogo-A antibody treatment and treadmill training in rats with incomplete spinal cord injury
Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females
Pilocytic astrocytoma of the optic pathway: a tumour deriving from radial glia cells with a specific gene signature
Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio)
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