About: Neurodegeneration

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Attributs	Valeurs
type	Concept
rdfs:label	Neurodegeneration
skos:inScheme	http://hub.abes.fr/referentiel/bmjarticlecategories
is Subject of	Why are upper motor neuron signs difficult to elicit in amyotrophic lateral sclerosis? Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights Cognitive decline and reduced survival in C9orf72 expansion frontotemporal degeneration and amyotrophic lateral sclerosis Dysfunction of the locus coeruleus-norepinephrine system and related circuitry in Parkinson's disease-related dementia Medial temporal lobe epilepsy is associated with neuronal fibre loss and paradoxical increase in structural connectivity of limbic structures The language profile of posterior cortical atrophy Risk for late-life re-injury, dementia and death among individuals with traumatic brain injury: a population-based study Lithium lacks effect on survival in amyotrophic lateral sclerosis: a phase IIb randomised sequential trial Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72 Intensity of human prion disease surveillance predicts observed disease incidence Posiphen as a candidate drug to lower CSF amyloid precursor protein, amyloid-β peptide and τ levels: target engagement, tolerability and pharmacokinetics in humans Cortical atrophy in presymptomatic Alzheimer's disease presenilin 1 mutation carriers White matter imaging helps dissociate tau from TDP-43 in frontotemporal lobar degeneration Can regional spreading of amyotrophic lateral sclerosis motor symptoms be explained by prion-like propagation? Retinal pathology as biomarker for cognitive impairment and Alzheimer's disease Regional brain volume differences in symptomatic and presymptomatic carriers of familial Alzheimer's disease mutations Amyloid imaging in Alzheimer's disease: comparison of florbetapir and Pittsburgh compound-B positron emission tomography Phosphorylated neurofilament heavy subunit (pNF-H) in peripheral blood and CSF as a potential prognostic biomarker in amyotrophic lateral sclerosis Perspectives on molecular targeted therapies and clinical trials for neurodegenerative diseases Cognitive impairment in the preclinical stage of dementia in FTD-3 CHMP2B mutation carriers: a longitudinal prospective study Motor axonal excitability properties are strong predictors for survival in amyotrophic lateral sclerosis Split hand syndrome in amyotrophic lateral sclerosis: different excitability changes in the thenar and hypothenar motor axons Differentiation of frontotemporal dementia from dementia with Lewy bodies using FP-CIT SPECT Flavour identification in frontotemporal lobar degeneration Neck weakness is a potent prognostic factor in sporadic amyotrophic lateral sclerosis patients Therapeutic strategies for tau mediated neurodegeneration Social cognition in neurodegenerative disorders: a systematic review Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality Elevated occipital β-amyloid deposition is associated with widespread cognitive impairment in logopenic progressive aphasia Midcingulate involvement in progressive supranuclear palsy and tau positive frontotemporal dementia Prevalence of adult Huntington's disease in the UK based on diagnoses recorded in general practice records TDP-43 frontotemporal lobar degeneration and autoimmune disease Fasciculation potentials and earliest changes in motor unit physiology in ALS

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