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NEUROLOGY

Rivista

Codice:

E117266

ISSN:

0028-3878

Dati Generali

Dati Generali

Pubblicazioni (151)

Ordina Pubblicazioni:

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A Pilot, Randomized, Placebo-Controlled, Trial of Lithium in Spinocerebellar Ataxia Type 2

Abstract

A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures

Articolo

A familial form of multiple sclerosis showing impaired ganglioside synthesis.

Articolo

A itochondrial tRNA (His) gene mutation causing pigmentary retinopathy and neurosensorial deafness

Articolo

A longitudinal study of determinants of hospitalization and lenght of stay in hospital among the Italian elderly

Contributo in Atti di convegno

A magnetization transfer histogram study of normal-appearing brain tissue in MS

Articolo

A missense mutation in the mitochondrial ND5 gene associated with a Leigh MELAS overlap syndrome

Articolo

A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2).

Articolo

A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1

Articolo

A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL.

Articolo

A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL.

Articolo

A novel mutation in SACS gene in a family from southern Italy

Articolo

A proposed dual role of neuromelanin in the pathogenesis of Parkinson's disease

Articolo

APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers

Articolo

Adenosine A2A and dopamine receptor interactions in basal ganglia of dopamine denervated rats.

Articolo

Alcohol consumption, mild cognitive impairment, and progression to dementia.

Articolo

Alterations of functional connectivity of the motor cortex in Fabry disease An RS-fMRI study

Articolo

Alzheimer disease risk associated with APOE4 is modified by STH gene polymorphism

Articolo

Amygdala dysplasia with temporal lobe epilepsy and obsessive-compulsive disorder: an fMRI/EEG study

Articolo

Association of gait and balance disorders with age-related white matter changes: the LADIS study.

Articolo

Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease.

Articolo

Association study of dopamine D2, D3 receptor gene polymorphisms with motor fluctuations in PD

Articolo

Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype.

Articolo

Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis

Articolo

Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene

Articolo

Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene.

Articolo

Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit.

Articolo

Author response: Alterations of functional connectivity of the motor cortex in Fabry disease: An RS-fMRI study

Articolo

Autosomal recessive Bethlem myopathy.

Articolo

Autosomal recessive myosclerosis myopathy is a collagen VI disorder.

Articolo

Axonal damage in multiple sclerosis plaques: a combined magnetic resonance imaging and 1H-magnetic resonance spectroscopy study

Articolo

Bilateral transverse sinus stenosis predicts IIH without papilledema in patients with migraine

Articolo

Blink reflex recovery cycle in patients with dystonic tremor: a cross-sectional study

Articolo

Blink reflex recovery cycle in patients with essential tremor associated with resting tremor.

Articolo

Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)

Articolo

Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)

Articolo

Brain atrophy and lesion load in a large population of patients with multiple sclerosis.

Articolo

Brain metabolic differences between sporadic and familial Alzheimer's disease.

Articolo

Broadened Friedreich's ataxia phenotype after gene cloning - Minimal GAA expansion causes late-onset spastic ataxia

Articolo

Broadened Friedreich's ataxia phenotype after gene cloning: Minimal GAA expansion causes late-onset spastic ataxia

Articolo

C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Articolo

CASES Investigators. Leukoaraiosis and intracerebral hemorrhage after thrombolysis in acute stroke.

Articolo

CIND and MCI in the Italian elderly: frequency, vascular risk factors, progression to dementia.

Articolo

COHORT study of the HSG. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

Articolo

CSF opening pressure: reference interval and the effect of body mass index

Articolo

Cerebral MR venography of transverse sinuses in subjects with normal CSF pressure.

Articolo

Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH.

Articolo

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.

Articolo

Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy.

Articolo

Clinical manifestations of intermediate allele carriers in Huntington disease

Articolo

Clozapine in Parkinson's disease tremor - Effects of acute and chronic administration

Articolo

Combined 7-T MRI and histopathologic study of normal and dysplastic samples from patients with TLE

Articolo

Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients.

Articolo

Conventional MRI and NOTCH3 gene screening in sporadic CADASIL.

Articolo

Course and prognosis in early-onset MS: comparison with adult-onset forms.

Articolo

Cysteine-sparing notch3 mutations: cadasil or cadasil variants?

Articolo

Diffusion tensor MRI changes in cerebellar structures of patients with familial essential tremor.

Articolo

Does lamotrigine use in pregnancy increase orofacial cleft risk relative to other malformations?

Articolo

Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD

Articolo

Education and occupation as proxies for reserve in aMCI converters and AD: FDG-PET evidence.

Articolo

Effects of Bacille Calmette-Guérin after the first demyelinating event in the CNS

Articolo

Epidemiology of distal symmetrical neuropathies in the Italian elderly.

Articolo

Estimating brain atrophy in clinical settings: linear measures of ventricular enlargement for evaluation of disease activity and long-term disability progression in Multiple Sclerosis

Abstract

European Registers of Stroke. Three-month stroke outcome: the European Registers of Stroke (EROS) investigators

Articolo

FUNCTIONAL MAGNETIC-RESONANCE-IMAGING (FMRI) OF MESIAL FRONTAL-CORTEX (SMA) DURING HAND MOVEMENTS

Abstract

Familial aggregation of Parkinson's disease: A population-based case-control study in Europe

Contributo in Atti di convegno

Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene.

Articolo

Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation

Articolo

Fixed dystonia unresponsive to pallidal stimulation improved by motor cortex stimulation.

Articolo

Frequency of stroke in Europe: A collaborative study of population-based cohorts

Articolo

Friedreich ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion

Abstract

Friedreich's ataxia after gene cloning. The sensitivity and specificity of clinical diagnosis

Articolo

GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy.

Articolo

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

Articolo

Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy.

Articolo

Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)

Articolo

Global investigation and meta-analysis of the C9orf72 (G(4)C(2))(n) repeat in Parkinson disease

Articolo

HLA B*44: protective effects in MS susceptibility and MRI outcome measures

Articolo

Has spinocerebellar ataxia type 2 a distinct phenotype? genetic and clinical study of an italian family

Articolo

Hippocampal and Thalamic Atrophy in Pharmaco-Sensitive Temporal Lobe Epilepsy: a VBM study

Articolo

Hippocampal mean diffusivity and memory in healthy elderly individuals: A cross-sectional study

Articolo

IV amantadine improves chorea in Huntington's disease: an acute randomized, controlled study

Articolo

Imaging of dopaminergic dysfunction with [I-123]FP-CIT SPECT in early-onset parkin disease

Articolo

Immunocytochemical study of nebulin in Duchenne muscular dystrophy.

Articolo

Incidence of dementia and major subtypes in Europe: A collaborative study of population-based cohorts

Articolo

Interferon beta-1a and atorvastatin combination therapy: 12-month results from an open-label, randomized, clinical study

Abstract

Intranasal midazolam for treating acute respiratory crises in a woman with stiff person syndrome

Articolo

Intraventricular tumor presenting as progressive supranuclear palsy-like phenotype

Articolo

Inverse occurrence of cancer and Alzheimer disease A population-based incidence study

Articolo

Is brain atrophy progression in RR-MS slowed by the association off atorvastatin and interferon beta-1a? Preliminary results from an open-label, randomized, clinical study

Abstract

Juvenile Huntington's disease presenting as progressive myoclonic epilepsy.

Articolo

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy

Articolo

LINKAGE AND LINKAGE DISEQUILIBRIUM IN FRIEDREICH'S DISEASE POSSIBLE ASSOCIATION BETWEEN GENETIC MARKERS AND ONSET AGES

Abstract

LMNA-associated myopathies: The Italian experience in a large cohort of patients.

Articolo

Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD.

Articolo

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease

Articolo

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

Articolo

Left caloric vestibular stimulation ameliorates right hemianesthesia.

Articolo

Limited chronic focal encephalitis: another variant of Rasmussen syndrome?

Articolo

Lithium in Multisystem Atrophy: Lack of Efficacy and Safety Issues

Abstract

MCI conversion to dementia and the APOE genotype: a prediction study with FDG-PET

Articolo

MRI evidence of mesial temporal sclerosis in sporadic "benign" temporal lobe epilepsy

Articolo

MRI measurements predict PSP in unclassifiable parkinsonisms: a follow-up study

Articolo

Magnetization transfer ratios in multiple sclerosis lesions enhancing after different doses of gadolinium

Articolo

Manometry combined with cervical puncture in idiopathic intracranial hypertension

Articolo

Mild cognitive impairment in drug-naive patients with PD is associated with cerebral hypometabolism

Articolo

Motor sensory neuropathy with minifascicle formation in a woman with normal karyotype

Articolo

Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.

Articolo

Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy.

Articolo

Myosin light chains and muscle pathology.

Articolo

Natalizumab Discontinuation after the 24th Course: Which Is Way? The TY-STOP Study

Abstract

Neurophysiological correlates of age-related changes in human motor function

Articolo

Neuropsychological assessment in children with absence epilepsy

Articolo

Obesity does not induce abnormal CSF pressure in subjects with normal cerebral MR venography.

Articolo

Phenotypic clustering of lamin A/C mutations in neuromuscular patients.

Articolo

Prevalence and risk factors of age-related cognitive decline: The Italian Longitudinal Study on Aging (ILSA)

Contributo in Atti di convegno

Prevalence of Parkinson's disease in Europe: A collaborative study of population-based cohorts

Articolo

Prevalence of dementia and major subtypes in Europe: A collaborative study of population-based cohorts

Articolo

Prognosis with dementia in Europe: A collaborative study of population-based cohorts

Articolo

Prognosis with stroke in Europe: A collaborative study of population-based cohorts

Articolo

Reader response: Increased resting cerebral blood flow in adult Fabry disease: MRI arterial spin labeling study

Articolo

Regional reductions of gray matter volume in familial dyslexia.

Articolo

Relationship between Clinical Aspects in Early Phases of Relapsing-Remitting Multiple Sclerosis and Subsequent Brain Volume Changes

Abstract

Reversible deep brain swelling causing REM behavior disorder

Articolo

Riluzole in cerebellar ataxia: a randomized, double-blind, placebo-controlled pilot trial

Articolo

Serum transferrin receptor levels in Friedreich's and other degenerative ataxias

Articolo

Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation.

Articolo

Sex differences in presentation, severity, and management of stroke in

Articolo

Sex differences in the incidence of dementing diseases in the Italian elderly: The ILSA study

Contributo in Atti di convegno

Sex-specific stroke prevalence and incidence of first-ever stroke in the elderly. A pooled analysis of European population-based study

Contributo in Atti di convegno

Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1

Articolo

Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly

Articolo

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine

Articolo

Teaching NeuroImages: Subacute encephalopathy in a young woman with THTR2 gene mutation.

Articolo

Teaching NeuroImages: pseudo-abnormal DaTscan findings in meningioma-induced parkinsonism.

Articolo

Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study

Articolo

The association of chronic hepatitis B and myopathy

Articolo

The differential effect of PD and normal aging on early explicit sequence learning

Articolo

The fragile X premutation presenting as postprandial hypotension.

Articolo

The midbrain to pons ratio: A simple and specific MRI sign of progressive supranuclear palsy.

Articolo

The parkin gene is not involved in late-onset Parkinson's disease

Articolo

Transverse sinus stenoses persist after normalization of the CSF pressure in IIH

Articolo

Treatment of first tonic-clonic seizure does not improve the prognosis of epilepsy

Articolo

Truncating Variants in RFC1 in Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome

Articolo

Two Novel CYP7131 Mutations in Italian Families with Autosomal Recessive Spastic Paraplegia: A Clinical and Genetic Study

Abstract

Vitamin D deficiency predicts cognitive decline in older men and women The Pro.VA Study

Articolo

When, where, and how the corpus callosum changes in MCI and AD: A multimodal MRI study

Articolo

White matter changes and diabetes predict cognitive decline in the elderly: the LADIS study.

Articolo

Worldwide distribution of PSEN1 Met146Leu mutation A large variability for a founder mutation

Articolo

Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation.

Articolo

[11C]PK11195 binding in Alzheimer disease and progressive supranuclear palsy.

Articolo

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