NEUROLOGICAL SCIENCES (TESTO STAMP.)

Rivista

Codice:

E117264

ISSN:

1590-1874

Dati Generali

Pubblicazioni (247)

"Identification and functional characterization of novel alleles in the promoter region of the serotonin transporter gene"

Abstract

A NOVEL MUTATION IN CX32 IDENTIFIED IN A PATIENT WITH DEMYELINATING SENSORY-MOTOR NEUROPATHY AND SECONDARY AXONOPATHY

Abstract

A PET study with [11-C]raclopride in Parkinson's disease: preliminary results on the effect of amantadine on the dopaminergic system

Articolo

A PET study with [11-C]raclopride in Parkinson's disease: preliminary results on the effect of amantadine on the dopaminergic system.

Articolo

A Proteomic approach to the study of the peripheral neuropathies:preliminary results

Abstract

A case of facioscapulohumeral muscular dystrophy and myasthenia gravis with positivity of anti-Ach receptor antibody: a fortuitous association?

Articolo

A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism.

Abstract

A gender specific association between the prodynorphin gene promoter and temporal lobe epilepsy.

Abstract

A genetic study on the role of thiamine transporters in a case of atrophic beri-beri

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A large Italian family with R521C mutation in the FUS/TLS gene

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A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease

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A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease

Abstract

A novel S379A TARDBP mutation associated to late-onset sporadic ALS

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A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia

Abstract

A novel mutation in the exon 7 of the NOTCH3 gene in a patient affected by CADASIL

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A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL

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A patient with Frontotemporal Dementia (FTD) and Motor Neuron Disease (MND) carrying the intron10+29 substitution in MAPT

Abstract

A rare case of multiple sclerosis and McArdle disease

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ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY

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APOE-4 allele and disease duration affect verbal memory in mild temporal lobe epilepsy.

Abstract

ASSOCIATION STUDY BETWEEN HFE, TF , TFR1 GENES AND PARKINSON S DISEASE

Abstract

ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses

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Aceruloplasminemia: a multimodal imaging study in an Italian family with a novel mutation

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Age at onset in multiple sclerosis

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Alpha synuclein in familial parkinson s disease and lewy body dementia.

Abstract

Alpha-synuclein promoter haplotypes and dementia in Parkinson s disease .

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Alpha2-macroglobulin gene polymorphisms in Alzheimer's disease

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Alzheimer s disease risk: analysis of the STH and apoE gene polymorphisms

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Amantadine in Huntington's disease: open-label video-blinded study

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Amiotrophic Lateral Sclerosis: a new missense mutation in SOD1 gene

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Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification

Abstract

Amyotrophic Lateral Sclerosis with brain white matter lesion in a young patient carrying FUS R521C mutation: case report.

Abstract

An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene

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An Italian child with myophosphorylase deficiency but with no detectable mutation in the exons of the PYGM gene

Abstract

An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample

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An axon regeneration signature in a Charcot-Marie-Tooth disease type 2 patient

Abstract

An intronic nucleotide change in the SPAST gene might produce an aberrant protein transcript

Abstract

An updated Italian normative dataset for the Stroop color word test (SCWT)

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Analysis of allelic distribution of apoE promoter polymorphism: relation to gender, age at onset, and e4 allele in a sample of sporadic AD patients

Abstract

Analytic information processing style in migraineurs

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Angiotensin converting enzyme (ACE) gene polymorphism in patients with frontotemporal dementia (FTD)

Abstract

Apolipoprotein E genotype and multiple sclerosis progression.

Abstract

Assessing executive function with the D-KEFS sorting test: normative data for a sample of the Italian adult population

Articolo

Assessment of Snaith-Hamilton Pleasure Scale (SHAPS): the dimension of anhedonia in Italian healthy sample.

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

Abstract

Association of tau gene polymorphism with Parkinson's disease

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Association of tau polymorphism with Parkinson's disease

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

Abstract

Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy.

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Association study of NACP-REP1 polymorphism and Parkinson's disease

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Atrophy of superior cerebellar peduncles in SCA7: a clinic-biological case report

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Autosomal Dominant Distal Motor Neuropathy: an Italian family not linked to known loci

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Autosomal dominant essential tremor: A novel family with anticipation

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BDNF Val66Met polymorphism and brain volumes in multiple sclerosis

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BDNF polymorphisms and outcome of post-traumatic vegetative state: results from an italian multicentric study

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BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION

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Babylonian knowledge about temporal lobe epilepsy: distinguishing mesial from lateral forms

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Biological factors and age-dependence of primary motor cortex experimental plasticity

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Body weight, levodopa pharmacokinetics and dyskinesia in Parkinson's disease

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Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS).

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Brown-Vialetto-Van Laere Syndrome: a case report of a family from Italy

Abstract

Burden and stress among stroke caregivers during the first 2 years after stroke. Results from a community-based study in Italy.

Abstract

CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis.

Abstract

CASP-9: a susceptibility locus for multiple sclerosis in Italy.

Abstract

CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY

Abstract

Camptocormia as presenting in lower motor neuron disease with TARDBP mutation: case report.

Articolo

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL): a proteiform neurological disease of expanding importance. Reasons for establishing an Italian Registry.

Articolo

Ceruloplasmin gene variations and Parkinson s disease: an association study in Southern Italian population.

Abstract

Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations

Abstract

Chromatic pattern-reversal electroretinograms (ChPERGs) are spared in Multiple System Atrophy compared with Parkinson s Disease.

Articolo

Chromatic pattern-reversal electroretinograms (ChPERGs) are spared in multiple system atrophy compared with Parkinson's disease.

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Clinic and genetic study in a family with a clinical picture of pantothenase kinase-associated neurodegeneration .

Abstract

Clinical and genetic analysis of a four-generation family with autosomal dominant cerebellar ataxia.

Abstract

Clinical and genetic study of an Italian family linked to SPG26 locus

Abstract

Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci

Articolo

Clinical, genetic and magnetic resonance findings in an Italian patient affected by l-2-hydroxyglutaric aciduria

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Cognitive impairment in multiple sclerosis: results in a sample of 593 Italian patients

Abstract

Color vision as a biological marker able to differentiate two phenotypically similar neurological diseases

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Color vision impairment: a preliminar comparison among Idiopathic Prkinson, Essential Tremor, Parkinsonism, Early Parkinson's Disease

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Color vision in multiple sclerosis. A preliminar investigation on 80 Calabrian males

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Color vision inpatients with Parkinson disease. Usefulness of three pseudoisochromatic tests

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Color vision study to assess the impaired retina-brain cortex pathway in type 2 diabetes: a pilot study in Calabria (Southern Italy).

Articolo

Colour vision in patients with Parkinson disease. Usefulness of three pseudoisochromatic tests

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Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2)

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Contribution of TARDBP mutations to Amyotrophic Lateral Sclerosis.

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Copy number variations and stroke

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Corpus callosum atrophy is associated with gait disorders in patients with leukoaraiosis.

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Could Mitochondrial Haplogroups Play A Role In Sporadic Amyotrophic Lateral Sclerosis?

Abstract

Currently used implementation methods in the area of stroke care and stroke prevention in Europe. The European Implementation Score (EIS) Project.

Abstract

DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS

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Diffusion tensor MRI changes in gray structures of the frontal-subcortical circuits in amyotrophic lateral sclerosis

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Dropped head syndrome in a patient with FTD-ALS caused by abnormal expansion of C9orf72 gene

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EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC

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EXPRESSION AND SUBCELLULAR LOCALIZATION OF Cu/Zn-SOD PROTEIN IN FIBROBLATS FROM A SPORADIC ALS PATIENT CARRYING THE N19S-SOD1 MUTATION

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Early-onset SCA17 with 43 TBP repeats: expanding the phenotype?

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Effect of febrile convulsions and APOE genotype on age at onset of mild non-lesional temporal lobe epilepsy

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Effect of nitric oxide on lymphocytes from sporadic amyotrophic lateral sclerosis patients:toxic or protective role?

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Effectiveness of an educational intervention to increase stroke awareness among high schoolstudents.

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Effectiveness of an educational intervention to increase stroke awareness among high schoolstudents. Results from a prospective study in Tuscany during the academic year 2014-2015.

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Electrophysiological evidence by single fibre electromyography of neuromuscular impairment in a case of Miller Fisher syndrome.

Articolo

Electrophysiological indexes of visual attention mechanisms for spatial and non-spatial features

Abstract

Epilepsy in popular Medicine from the Classic Age to the Modern Age: a study on elk hoof as an original treatment

Articolo

Evidence of genetic heterogeneity in autosomal dominant nocturnal frontal lobe epilepsy

Abstract

Evidence of genetic heterogeneity in families with febrile seizures

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Evidences of emerging pain consciousness during prenatal development: a narrative review

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Expression of multidrug resistance type 1 gene (MDR1) P-glycoprotein in intractable epilepsy with different aetiologies: a double-labelling and electron microscopy study.

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FKRP expression in Lymphoblastoid cell lines:a human cellular model to study the impact of the mutations on the protein functionality

Abstract

FRAGILE X PREMUTATION ALLELES IN MOVEMENT DISORDERS

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FUS PROTEIN IS MISLOCALIZED IN THE CYTOPLASM OF CULTURED SKIN FIBROBLASTS FROM PRECLINICAL FUS P525L MUTATION CARRIERS

Abstract

Fast and accurate SNVs and CNVs screening in Parkinson's Disease Patients using Next-Generation approach

Abstract

Frequency analysis of autosomal dominant spinocerebellar ataxia (AD-SCA) in the patients from southern Italy

Abstract

Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype

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Functional Cortical Changes In Amyotrophic Lateral Sclerosis: An FMRI Study In The Early Stage Of The Disease

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Functional roles of dystrophin and of associated proteins. New insights for the sarcoglycans.

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Further insight on A-wave in acute and chronic demyelinating neuropathies.

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G-463A myeloperoxidase polymorphism and parkinson s disease

Abstract

G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSON S DISEASE

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G56S and ARG143SER mutations in CAV3 and FKRP gene respectively contribute to the expression of phenotypic characteristics of an LGMD patient of southern Italy

Abstract

GENETIC COUNSELLING IN ALS: FACTS, UNCERTAINTIES AND RECOMMENDATIONS

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GENETIC STUDY OF SCN1A-RELATED EPILEPSIES IN SOUTHERN ITALY

Abstract

GIGYF2 (TRNC15) MUTATION ANALYSIS IN PATIENTS WITH FAMILIAL PARKINSON DISEASE WITH AUTOSOMAL-DOMINANT TRANSMISSION

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Gender-related effect of clinical and genetic variables on the cognitive impairment in MS.

Abstract

Genome wide linkage of a large serbian family with GEFS+.

Abstract

Gly2019Ser Mutation in the LRRK2 gene and Parkinson s disease in the Italian population.

Abstract

Guidelines for the diagnosis of dementia and Alzheimer's disease

Articolo

Histone H4K16 hypoacetylation in a PKAN lymphoblastoid cell line from a patients compound heterozygous for the PANK2 gene: a MALDI-ISD study

Abstract

Horizontal gaze palsy with progressive scoliosis: is scoliosis linked to ROBO3 mutations?

Articolo

Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case

Abstract

Hospital-discharge data underestimate hemorrhagic stroke events: data from a multicenter validation survey in the Florence area (Italy).

Abstract

Hospital-discharge-data underestimate hemorragic stroke events: data from a multicenter validation survey in the Florence area (Italy).

Abstract

Huntington's disease-like syndrome: a case report

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Hyperacute stroke management before and after an integrated healthcare system introduction in Elba island-Italy

Abstract

IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME

Abstract

INTERACTION BETWEEN DOPAMINE AND ADENOSINE A2A RECEPTORS AS A BASIS FOR THE TREATMENT OF PARKINSON'S DISEASE

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Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset

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Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset.

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Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy.

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Incidence of Parkinsonism and Parkinson s disease in a general population: data from the second follow-up survey of the Italian Longitudinal study on Aging (ILSA).

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Interaction between Apolipoprotein-E4 and traumatic brain injury in patients with Alzheimer?s disease and mild cognitive impairment.

Abstract

Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis.

Abstract

Is color vision a diagnostic sign in different neurodegenerative diseases?

Abstract

Italian Neurological Society guidelines for the diagnosis of dementia: revision I

Articolo

Italian multicentre observational study of the prevalence of CCSVI in multiple sclerosis (CoSMo study): Rationale, design, and methodology

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Italian studies on early onset multiple sclerosis: the present and the future

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Lack of association between GRIN2B gene coding for 2B subunit of the NMDA receptor and Alzheimer's disease

Abstract

Lifestyle and vascular risk factors for Alzheimer's disease.

Abstract

Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy .

Abstract

Linkage and mutational study in two families with Familial Hemiplegic Migraine .

Abstract

Listening to the neurological teams for multiple sclerosis: the SMART project

Articolo

MALDI-TOF-MS peptide patterns in cerebrospinal fluid from patients withy idiopathic intracranial hypertension.

Abstract

MTDNA HAPLOGROUP K IS PROTECTIVE AGAINST PD IN ITALIAN POPULATION

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MUTATIONAL ANALISYS OF GJB1, MPZ AND PMP22 GENES IN CMT PATIENTS FROM SOUTHERN ITALY

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MUTATIONAL DETECTION OF EARLY ONSET PARKINSON DISEASE GENES IN PATIENTS FROM SOUTHERN ITALY

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Monitoring the implementation of the State-Regional Council agreement 03/02/2005 as to the management of acute stroke events: a comparison of the Italian regional legislations

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Multiple sclerosis in Italy: cost-of-illness study

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Multiple sclerosis in children under 10 years of age

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Mutational analysis of SCN2A gene in italian families with benign familial neonatal-infantile seizures (BFNIS) .

Abstract

Mutational and linkage analysis in three calabrian families with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

Abstract

Mutational screening of the CAPN3 in LGMD patients from Southern Italy.

Abstract

Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks

Articolo

NOTCH3 PROTEIN LOCALIZATION IN SKIN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE MICROSCOPY STUDY

Abstract

NOTCH3 gene mutations and mtDNA variations

Abstract

Natalizumab is effective in multiple sclerosis patients switching from other disease modifying therapies in clinical practice

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Natalizumab is effective in multiple sclerosis patients switching from other disease modifying therapies in clinical practice.

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Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis

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Neuropsychological heterogeneity in patients with primary familial brain calcification due to a novel mutation in SLC20A2

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No evidence of association between Alpha2 macroglobulin gene and Parkinson' s disease in a case-control sample

Abstract

No evidence of association between alpha 2 macroglobulin gene and Parkinson's disease in a case-control sample

Abstract

Non-convulsive status epilepticus during lithium treatment at therapeutic doses

Articolo

Normal immunofluorescence pattern of skin basement membranes in a family with porencephaly due to COL4A1 G749S mutation

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Oxidative stress in Parkinson s disease: Implication for Glutathione transferase enzyme activity.

Articolo

Oxidative stress in patients with myotonic dystrophy.

Abstract

PARKIN, PINK1 AND DJ-1 HETEROZYGOUS MUTATIONS IN SOUTHERN ITALIAN PATIENTS WITH EARLY-ONSET PARKINSONISM

Abstract

PATTERN OF PROTEIN EXPRESSIONS IN SURAL NERVE OF CMT1A PATIENTS WITH CHROMOSOME 17p11.2 DUPLICATION

Abstract

Parkin mutations in patients with early onset parkinsonism .

Abstract

Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome

Articolo

Polymorphism Ile587val in the eIF2B5 gene as susceptibility factor in multiple sclerosis

Abstract

Polymorphisms of dopamine D1 and D2 receptor genes influence penetrance in dopa-responsive dystonia .

Abstract

Position paper of the Italian Society for the study of Dementias (Sindem) on the proposal of a new Lexicon on Alzheimer disease

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Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome

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Predictive factors of neutralizing antibodies development in relapsing-remitting multiple sclerosis patients on interferon Beta-1b therapy

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Presenilin-2 gene mutation presenting as Lewy Body dementia?

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Prevalence of atrial fibrillation in the Italian elderly population. Final results from the Progetto FAI. La Fibrillazione Atriale in Italia.

Abstract

Prospective evaluation of post-stroke rehabilitation in Florence, Italy

Abstract

Prospective study of coffee consumption and risk of Parkinson disease. The Italian Longitudinal Study on Aging.

Abstract

Quality indicators in acute stroke care. A prospective survey in 13 Italian Regions. The National Research Programme: How to guarantee adherence to effective interventions in stroke care.

Abstract

Recommendations of the Sleep Study Group of the Italian Dementia Research Association (SINDem) on clinical assessment and management of sleep disorders in individuals with mild cognitive impairment and dementia: a clinical review.

Articolo

Relevance of pre-hospital stroke-code activation in the acute stroke care: a review.

Abstract

Retrospective analysis of two large cohorts of AD and non-AD patients. A simple method for the identification of apoE genotypes by positive/negative polymerase chain reaction product

Abstract

SPORADIC ALS AND VCP GENE ANALISYS IN SOUTHERN ITALY

Abstract

SURAL NERVE PROTEIN PROFILE BY MATRIX ASSISTED LASER DESORPTION IONIZATION-TIME OF FLIGHT MASS SPECTROMETRY (MALDI-TOF MS) DIRECT ANALYSIS: PRELIMINARY DATA.

Articolo

Sca17 as cause of early-onset dementia in sothern Italy: report of a new family.

Abstract

Screening for PINK1 mutations in patients with early- and late-onset Parkinson disease

Abstract

Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [(11)C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2)

Articolo

Stroke in the Italian elderly population. Incidence and impact on survival and activities of daily living. The ILSA Study

Abstract

Stroke in the acute phase. A preliminary report from the North Florence Stroke Registry and the Sesto Fiorentino Study. The European Registers of stroke (EROS).

Articolo

Stroke knowledge in Italy

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Subcortical Motor Plasticity In Patients With Sporadic Amyotrophic Lateral Sclerosis

Abstract

Successful performance of the Tuscany Stroke Network: a before-and-after study

Abstract

Symptomatic spinal cord metastasis from cerebral oligodendroglioma.

Articolo

TRIM32 as susceptibility gene for pathological cardiac hypertrophy

Abstract

Targeted Next-Generation Sequencing revealed rare variations in two siblings affected by late onset Parkinson's disease.

Abstract

The "eye of the tiger" sign in pure akinesia with gait freezing

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The FRAGAMP study: environmental and genetic factors in Parkinson's disease, methods and clinical features.

Articolo

The HFE p.His63Asp polymorphism modifies als outcome in patients with SOD1 mutations

Abstract

The Italian Stroke-APP: www.ictus3R

Abstract

The Italian stroke-app: ICTUS3R

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The Parkin gene is not a major susceptibility locus for typical lare-onset Parkinson's disease

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The Tuscany Stroke Network: Team is Brain

Abstract

The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis .

Abstract

The burden of atrial fibrillation in the Italian elderly population. Preliminary results from the first year of activity of the Progetto FAI. La Fibrillazione Atriale in Italia

Abstract

The case of encephalitis in a COVID-19 pediatric patient

Articolo

The effect of Parkinson's disease and frontal lobe lesions on serial learning

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The elk's nail treating the epilepsy between classic age and modernity age

Abstract

The end of the central dogma of neurobiology: stem cells and neurogenesis in adult CNS.

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The impact of first world war on post traumatic psychiatric symptoms in soldiers. A retrospective study analysis of 498 soldiers admitted in the psychiatric hospital of Girifalco (Catanzaro)

Abstract

The impact of first world war on post-traumatic psychiatric symptoms in soldiers. A retrospective study analysis of 498 soldiers admitted in the psychiatric hospital of Girifalco (Catanzaro)

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The impact of sexual abuse on psychopathology of patients with psychogenic nonepileptic seizures

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The minor Alois Alzheimer before the discovery of the eponymous disorder

Abstract

The minor Alois Alzheimer before the discovery of the eponymous disorder

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The neurological syphilis within some not-medical works between nineteenth and twentieth century

Abstract

The nicotinic receptor B2 subunit on chromosome 1 is mutated in nocturnal frontal lobe epilepsy

Abstract

The parkin gene is not a major susceptibility locus for typical late-onset Parkinson's disease

Articolo

The role of sphingolipids in the control of skeletal muscle function: A review.

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The status of dopamine nerve terminal in Parkinson s disease and essential tremor: A PET study with the tracer [11-C]FE-CIT

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Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus

Abstract

Thymosin beta 4 is overexpressed in Cerebrospinal fluid of Creutzfeldt-Jacob disease patients: a MALDI-TOF MS protein profiling study.

Abstract

Treatment of multiple sclerosis with interferon beta in clinical practice: 2-year follow-up data from the South Italy Mobile MRI Project.

Articolo

Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL

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Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer s Disease in southern Italy.

Abstract

Two novel Nav1.1 mutations associated with Generalized Epilepsy with Febrile Seizures Plus

Abstract

Two novel Nav11 mutations associated with Generalized Epilepsy with Febrile Seizures Plus

Abstract

Updating on Italian Stroke Units: the "CCM Study"

Articolo

VLA-4 and Multiple Sclerosis in Italian population.

Abstract

Validation of the Guidelines for the Diagnosis of Dementia and Alzheimer's Disease of the Italian Neurological Society. Study in 72 Italian neurological centres and 1549 patients

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Validity of the minimal assessment of cognitive function in multiple sclerosis (MACFIMS) in the Italian population

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Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study.

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Variants in CAV3, TRIM32 and PSN2 genes suggest an additive effect in the development of dilated cardiomyopathy in a family of south Italy

Abstract

Vascular factors predict chronic-idiopathic distal symmetric neuropathy (CI-DSN) in the elderly general population. Data from the Italian Longitudinal Study on Aging (ILSA).

Articolo

Vascular factors predict polyneuropathy in a non-diabetic elderly population.

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Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjogren Syndrome

Abstract

Vitamins prevent the neurological symptoms in their deficiency disorders

Abstract

Vitamins prevent the neurological symptoms in their deficiency disorders

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Voluntary selective big toe dorsal flection: pseudo-Babinski phenomenon?

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oFunctional Neuroimaging in De Novo Parkinson's Disease with Rem sleep behavior disorder.

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oThe 16 item-printed word version of the free and cued selective reminding test (FCSRT): normal values in an Italian population.

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oThe Stroop color and word test (SCWT): preliminary normal data in an Italian population.

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No Results Found