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BRAIN (PRINT)
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Codice:
E024689
ISSN:
0006-8950
Dati Generali
Dati Generali
Pubblicazioni (59)
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Ordina Pubblicazioni:
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300 Hz subtalamic oscillations in Parkinson's disease
Articolo
Abnormalities of sensorimotor integration in focal dystonia: a transcranial magnetic stimulation study.
Articolo
Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13.
Articolo
Alpha-synuclein targets GluN2A NMDA receptor subunit causing striatal synaptic dysfunction and visuospatial memory alteration
Articolo
Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study.
Articolo
Altered cortical-cerebellar circuits during verbal working memory in essential tremor
Articolo
Animals lacking link protein have attenuated perineuronal nets and persistent plasticity
Articolo
Apparent diffusion coefficient measurements of the middle cerebellar peduncle differentiate the Parkinson variant of MSA from Parkinson's disease and progressive supranuclear palsy
Articolo
Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafness
Articolo
Blurring in patients with temporal lobe epilepsy: clinical, high-field imaging and ultrastructural study
Articolo
Brain abnormalities underlying altered activation in dyslexia: a voxel based morphometry study
Articolo
Causes of cross-over in unilateral neglect: between-group comparisons, within-patient dissociations and eye movements
Articolo
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): Clinical, neuroimaging, pathological and genetic study of a large Italian family
Articolo
Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants.
Articolo
Decreased carbon-11-flumazenil binding in early Alzheimer's disease.
Articolo
Does cerebrovascular disease affect the coupling between neuronal activity and local hemodinamics?
Articolo
Dopamine release during sequential finger movements in health and Parkinson's disease: a PET study.
Articolo
Dopamine-dependent early synaptic and motor dysfunctions induced by ?-synuclein in the nigrostriatal circuit
Articolo
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders
Articolo
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy
Articolo
Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice.
Articolo
Epilepsy Subtype-Specific Copy Number Burden Observed in a Genome-Wide Study of 17 458 Subjects
Articolo
Hereditary demyelinating neuropathy of infancy: a genetically complex syndrome
Articolo
Idiopathic partial epilepsy with auditory features (IPEAF ) a clinical and genetic study of 53 sporadic cases
Articolo
Impairment of auditory spatial localization in congenitally blind human subjects
Articolo
Interplay between spinal cord and cerebral cortex metabolism in amyotrophic lateral sclerosis
Articolo
Intra-cortical connectivity in Multiple Sclerosis: a neurophysiological approach.
Articolo
Intra-cortical connectivity in multiple sclerosis: A neurophysiological approach
Articolo
LRRK2 G2019S kinase activity triggers neurotoxic NSF aggregation
Articolo
Late-onset Parkinsonism in NFkB/c-Rel-deficient mice
Articolo
Magnetic resonance imaging markers of Parkinson's disease nigrostriatal signature
Articolo
Metastatic group 3 medulloblastoma is driven by PRUNE1 targeting NME1-TGF-?-OTX2-SNAIL via PTEN inhibition
Articolo
Microglial activation and tau burden predict cognitive decline in Alzheimer's disease.
Articolo
Microglial large extracellular vesicles propagate early synaptic dysfunction in Alzheimer's disease
Articolo
Molecular pathology and synaptic loss in primary tauopathies: an 18F-AV-1451 and 11C-UCB-J PET study
Articolo
Motor and emotional behaviours elicited by electrical stimulation of the human cingulate cortex
Articolo
Motor learning and metaplasticity in striatal neurons: relevance for Parkinson's disease
Articolo
Mutation in senataxin alters the mechanism of R-loop resolution in amyotrophic lateral sclerosis 4
Articolo
Nerve growth factor improves visual loss in childhood optic gliomas: a randomized, double-blind, phase II clinical trial.
Articolo
Neurobiological mechanisms underlying emotional processing in Relapsing-Remitting Multiple Sclerosis
Articolo
Neuroinflammation and protein aggregation co-localize across the frontotemporal dementia spectrum.
Articolo
No reversal of the Oppel-Kundt illusion with short stimuli: confutation of the space anisometry interpretation of neglect and 'cross-over' in line bisection
Articolo
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
Articolo
On the pathogenesis of collagen VI muscular dystrophies--comment on article of Hicks et al.
Articolo
PMP22 messenger RNA levels in skin biopsies: Testing the effectiveness of a Charcot-Marie-Tooth 1A biomarker
Articolo
PRRT2 controls neuronal excitability by negatively modulating Na
+
channel 1.2/1.6 activity
Articolo
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis
Articolo
Polygenic burden in focal and generalized epilepsies
Articolo
Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies
Articolo
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis
Articolo
Senataxin modulates neurite growth through fibroblast growth factor 8 signalling.
Articolo
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study
Articolo
The 'headache tree' via umbellulone and TRPA1 activates the trigeminovascular system.
Articolo
The P2Y-like receptor GPR17 as a sensor of damage and a new potential target in spinal cord injury
Articolo
The chemokine CXCL12 mediates the anti-amyloidogenic action of painless human nerve growth factor
Articolo
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.
Articolo
The synaptic function of parkin
Articolo
The transcription factor orthodenticle homeobox 2 influences axonal projections and vulnerability of midbrain dopaminergic neurons
Articolo
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
Articolo
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