About: http://hub.abes.fr/bmj/periodical/jnnp/2009/volume_80/issue_12/w

Documentation

scienceplus.abes.fr version Bêta

scienceplus.abes.fr | explorer

À propos de : http://hub.abes.fr/bmj/periodical/jnnp/2009/volume_80/issue_12/w Goto Sponge NotDistinct Permalink

Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/bmj/periodical/jnnp/2009/volume_80
has manifestation of work	http://hub.abes.fr/bmj/periodical/jnnp/2009/volume_80/issue_12/m/print http://hub.abes.fr/bmj/periodical/jnnp/2009/volume_80/issue_12/m/web
Date Copyrighted	2009
Rights	BMJ Publishing Group Ltd. All rights reserved.
issue	12
is Is Part Of of	Double depressor palsy caused by bilateral paramedian thalamic infarcts The old age psychiatry handbook. A practical guide Functional magnetic resonance imaging study on dysphagia after unilateral hemispheric stroke: a preliminary study The diagnostic value of provocative clinical tests in ulnar neuropathy at the elbow is marginal Behavioural abnormalities associated with rapid deterioration of language functions in semantic dementia respond to sertraline MR spectroscopy indicates diffuse multiple sclerosis activity during remission New acute and chronic black holes in patients with multiple sclerosis randomised to interferon beta-1b or glatiramer acetate Johann Cristian Reil on the 200th anniversary of the first description of the insula (1809) Posterior circulation strokes without systemic involvement as the presenting feature of Fabry disease The neurology of olfaction Tongue pseudohypertrophy in idiopathic hypoglossal nerve palsy Sporadic inclusion body myositis: evidence of a link between inflammation, cell stress and β-amyloid deposition Somatosensory temporal discrimination in patients with primary focal dystonia Proinflammatory cell stress in sporadic inclusion body myositis muscle: overexpression of αB-crystallin is associated with amyloid precursor protein and accumulation of β-amyloid Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia Drain associated meningitis and ventriculitis remains a pivotal problem in neurointensive care: to understand their causes we need better surveillance data Diagnosis and new treatments in genetic neuropathies Impact of posterior communicating artery on basilar artery steno-occlusive disease Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations Clinical and mutational spectrum of limb-girdle muscular dystrophy type 2I in 11 French patients Can mutations of prion protein shed light on its normal function? Assessment of spinal somatosensory systems with diffusion tensor imaging in syringomyelia Long-term mortality and vascular event risk after aneurysmal subarachnoid haemorrhage A reappraisal of the value of lateral spread response monitoring in the treatment of hemifacial spasm by microvascular decompression Prospective surveillance of drain associated meningitis/ventriculitis in a neurosurgery and neurological intensive care unit A case of stroke induced micrographia Epilepsy in women Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology Immunotherapy: responsive autoimmune encephalopathy associated with bullous pemphigoid Epidemiology and pathophysiology of falls in facioscapulohumeral disease Validity of diagnostic criteria for chronic inflammatory demyelinating polyneuropathy: a multicentre European study Genetic Creutzfeldt-Jakob disease mimicking variant Creutzfeldt-Jakob disease Characteristics of abnormal eating behaviours in frontotemporal lobar degeneration: a cross-cultural survey

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata