Neurological sciences

Label

• Neurological sciences (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSON’S DISEASE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• Alzheimer’s disease risk: analysis of the STH and apoE gene polymorphisms (Abstract in rivista) (Prodotto della ricerca)
• Clinical, genetic and magnetic resonance findings in an Italian patient affected by L: -2-hydroxyglutaric aciduria. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• MALDI-TOF-MS peptide patterns in cerebrospinal fluid from patients withy idiopathic intracranial hypertension. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• FRAGILE X PREMUTATION ALLELES IN MOVEMENT DISORDERS (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• 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 in rivista) (Prodotto della ricerca)
• G-463A myeloperoxidase polymorphism and parkinson’s disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• A NOVEL MUTATION IN CX32 IDENTIFIED IN A PATIENT WITH DEMYELINATING SENSORY-MOTOR NEUROPATHY AND SECONDARY AXONOPATHY (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Non-convulsive status epilepticus during lithium treatment at therapeutic doses (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Corpus callosum atrophy is associated with gait disorders in patients with leukoaraiosis. (Articolo in rivista) (Prodotto della ricerca)
• Expression of multidrug resistance type 1 gene (MDR1) P-glycoprotein in intractable epilepsy with different aetiologies: a double-labelling and electron microscopy study. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• 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 in rivista) (Prodotto della ricerca)
• Gender-related effect of clinical and genetic variables on the cognitive impairment in MS. (Abstract/Poster in rivista) (Prodotto della ricerca)
• APOE-4 allele and disease duration affect verbal memory in mild temporal lobe epilepsy. (Abstract/Poster in rivista) (Prodotto della ricerca)
• Italian studies on early onset multiple sclerosis: the present and the future (Articolo in rivista) (Prodotto della ricerca)
• Amiotrophic Lateral Sclerosis: a new missense mutation in SOD1 gene (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations (Abstract in rivista) (Prodotto della ricerca)
• Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study. (Articolo in rivista) (Prodotto della ricerca)
• “Linkage and mutational study in two families with Familial Hemiplegic Migraine”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• “Polymorphisms of dopamine D1 and D2 receptor genes influence penetrance in dopa-responsive dystonia”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• “Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome (Articolo in rivista) (Prodotto della ricerca)
• Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL (Abstract/Poster in rivista) (Prodotto della ricerca)
• A novel mutation in the exon 7 of the NOTCH3 gene in a patient affected by CADASIL (Abstract in rivista) (Prodotto della ricerca)
• Oxidative stress in Parkinson’s disease: Implication for Glutathione transferase enzyme activity. (Abstract/Poster in rivista) (Prodotto della ricerca)
• An intronic nucleotide change in the SPAST gene might produce an aberrant protein transcript (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Body weight, levodopa pharmacokinetics and dyskinesia in Parkinson's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Clinical and genetic analysis of a four-generation family with autosomal dominant cerebellar ataxia. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Currently used implementation methods in the area of stroke care and stroke prevention in Europe. The European Implementation Score (EIS) Project. (Abstract in rivista) (Prodotto della ricerca)
• ASSOCIATION STUDY BETWEEN HFE, TF , TFR1 GENES AND PARKINSON’S DISEASE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• Updating on Italian Stroke Units: the \"CCM Study\" (Articolo in rivista) (Prodotto della ricerca)
• PARKIN, PINK1 AND DJ-1 HETEROZYGOUS MUTATIONS IN SOUTHERN ITALIAN PATIENTS WITH EARLY-ONSET PARKINSONISM (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• MUTATIONAL DETECTION OF EARLY ONSET PARKINSON DISEASE GENES IN PATIENTS FROM SOUTHERN ITALY (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• MTDNA HAPLOGROUP K IS PROTECTIVE AGAINST PD IN ITALIAN POPULATION (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Genome wide linkage of a large serbian family with GEFS+. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• A patient with Frontotemporal Dementia (FTD) and Motor Neuron Disease (MND) carrying the intron10+29 substitution in MAPT (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Vascular factors predict polyneuropathy in a non-diabetic elderly population. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Mutational screening of the CAPN3 in LGMD patients from Southern Italy. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• GENETIC STUDY OF SCN1A-RELATED EPILEPSIES IN SOUTHERN ITALY (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• The status of dopamine nerve terminal in Parkinson’s disease and essential tremor: A PET study with the tracer [11-C]FE-CIT (Articolo in rivista) (Prodotto della ricerca)
• IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• CASP-9: a susceptibility locus for multiple sclerosis in Italy. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• SPORADIC ALS AND VCP GENE ANALISYS IN SOUTHERN ITALY (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• \"Identification and functional characterization of novel alleles in the promoter region of the serotonin transporter gene\" (Abstract in rivista) (Prodotto della ricerca)
• “Mutational analysis of SCN2A gene in italian families with benign familial neonatal-infantile seizures (BFNIS)”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• “Clinic and genetic study in a family with a clinical picture of pantothenase kinase-associated neurodegeneration”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• “Alpha-synuclein promoter haplotypes and dementia in Parkinson’s disease”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• The minor Alois Alzheimer before the discovery of the eponymous disorder (Abstract/Comunicazione in rivista) (Prodotto della ricerca)
• Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Alpha synuclein in familial parkinson’s disease and lewy body dementia. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Glucocerebrosidase gene mutations are associated with Parkinson’s disease in a population from Souther Italy. (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Sca17 as cause of early-onset dementia in sothern Italy: report of a new family. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• An Italian child with myophosphorylase deficiency but with no detectable mutation in the exons of the PYGM gene (Abstract/Poster in rivista) (Prodotto della ricerca)
• The FRAGAMP study: environmental and genetic factors in Parkinson's disease, methods and clinical features. (Articolo in rivista) (Prodotto della ricerca)
• Parkin mutations analysis in patients with sporadic early-onset Parkinson’s disease (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• DJ-1 gene confers susceptibility to Parkinson’s disease. (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Ceruloplasmin gene variations and Parkinson’s disease: an association study in Southern Italian population. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• BDNF Val66Met polymorphism and brain volumes in multiple sclerosis (Articolo in rivista) (Prodotto della ricerca)
• Symptomatic spinal cord metastasis from cerebral oligodendroglioma. (Articolo in rivista) (Prodotto della ricerca)
• BDNF polymorphisms and outcome of post-traumatic vegetative state: results from an italian multicentric study (Abstract in rivista) (Prodotto della ricerca)
• A genetic study on the role of thiamine transporters in a case of atrophic beri-beri (Abstract in rivista) (Prodotto della ricerca)
• Electrophysiological evidence by single fibre electromyography of neuromuscular impairment in a case of Miller Fisher syndrome. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• The \"eye of the tiger\" sign in pure akinesia with gait freezing (Articolo in rivista) (Prodotto della ricerca)
• Predictive factors of neutralizing antibodies development in relapsing-remitting multiple sclerosis patients on interferon Beta-1b therapy (Articolo in rivista) (Prodotto della ricerca)
• Colour vision in patients with Parkinson disease. Usefulness of three pseudoisochromatic tests (Abstract/Comunicazione in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1106)
• 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 in rivista) (Prodotto della ricerca)
• Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. (Articolo in rivista) (Prodotto della ricerca)
• Vitamins prevent the neurological symptoms in their deficiency disorders (Abstract/Comunicazione in rivista) (Prodotto della ricerca)
• 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/Comunicazione in rivista) (Prodotto della ricerca)
• ADULT ONSET TAY-SACHS ASSOCIATED WITH ’-HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Could Mitochondrial Haplogroups Play A Role In Sporadic Amyotrophic Lateral Sclerosis? (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Functional Cortical Changes In Amyotrophic Lateral Sclerosis: An FMRI Study In The Early Stage Of The Disease (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Subcortical Motor Plasticity In Patients With Sporadic Amyotrophic Lateral Sclerosis (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Clinical and genetic study of an Italian family linked to SPG26 locus (Abstract in rivista) (Prodotto della ricerca)
• Analytic information processing style in migraineurs (Articolo in rivista) (Prodotto della ricerca)
• A large Italian family with R521C mutation in the FUS/TLS gene (Abstract/Poster in rivista) (Prodotto della ricerca)
• Brown-Vialetto-Van Laere Syndrome: a case report of a family from Italy (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Contribution of TARDBP mutations to Amyotrophic Lateral Sclerosis. (Abstract in rivista) (Prodotto della ricerca)
• GENETIC COUNSELLING IN ALS: FACTS, UNCERTAINTIES AND RECOMMENDATIONS (Abstract in rivista) (Prodotto della ricerca)
• ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses (Articolo in rivista) (Prodotto della ricerca)
• Polymorphism Ile587val in the eIF2B5 gene as susceptibility factor in multiple sclerosis (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Autosomal Dominant Distal Motor Neuropathy: an Italian family not linked to known loci (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Further insight on A-wave in acute and chronic demyelinating neuropathies. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• NOTCH3 gene mutations and mtDNA variations (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• The effect of Parkinson's disease and frontal lobe lesions on serial learning (Articolo in rivista) (Prodotto della ricerca)
• Italian Neurological Society guidelines for the diagnosis of dementia: revision I (Articolo in rivista) (Prodotto della ricerca)
• The end of the central dogma of neurobiology: stem cells and neurogenesis in adult CNS. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Italian multicentre observational study of the prevalence of CCSVI in multiple sclerosis (CoSMo study): Rationale, design, and methodology (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• GIGYF2 (TRNC15) MUTATION ANALYSIS IN PATIENTS WITH FAMILIAL PARKINSON DISEASE WITH AUTOSOMAL-DOMINANT TRANSMISSION (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• NOTCH3 PROTEIN LOCALIZATION IN SKIN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE MICROSCOPY STUDY (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• 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 (Articolo in rivista) (Prodotto della ricerca)
• Frequency analysis of autosomal dominant spinocerebellar ataxia (AD-SCA) in the patients from southern Italy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Position paper of the Italian Society for the study of Dementias (Sindem) on the proposal of a new Lexicon on Alzheimer disease (Articolo in rivista) (Prodotto della ricerca)
• Thymosin beta 4 is overexpressed in Cerebrospinal fluid of Creutzfeldt-Jacob disease patients: a MALDI-TOF MS protein profiling study. (Abstract/Comunicazione in rivista) (Prodotto della ricerca)
• Autosomal dominant essential tremor: A novel family with anticipation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• “Parkin mutations in patients with early onset parkinsonism”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL): a proteiform neurological disease of expanding importance. Reasons for establishing an Italian Registry. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Treatment of multiple sclerosis with interferon beta in clinical practice: 2-year follow-up data from the South Italy Mobile MRI Project. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Association study of NACP-REP1 polymorphism and Parkinson's disease (Abstract in rivista) (Prodotto della ricerca)
• Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• VLA-4 and Multiple Sclerosis in Italian population. (Abstract/Poster in rivista) (Prodotto della ricerca)
• Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer’s Disease in southern Italy. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Lack of association between GRIN2B gene coding for 2B subunit of the NMDA receptor and Alzheimer's disease (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis’. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• 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). (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• The Tau haplotype contributes to susceptibility to Parkinson’s disease in a Souther Italy population. (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Pink1 mutations and the risk of Parkinson’s disease in family members of Southern Italy (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). (Abstract/Comunicazione in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1106)
• Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• 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 in rivista) (Prodotto della ricerca)
• Clinical, genetic and magnetic resonance findings in an Italian patient affected by l-2-hydroxyglutaric aciduria (Articolo in rivista) (Prodotto della ricerca)
• Prospective study of coffee consumption and risk of Parkinson disease. The Italian Longitudinal Study on Aging. (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Burden and stress among stroke caregivers during the first 2 years after stroke. Results from a community-based study in Italy. (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• 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 in rivista) (Prodotto della ricerca)
• Interaction between Apolipoprotein-E4 and traumatic brain injury in patients with Alzheimer?s disease and mild cognitive impairment. (Abstract/Poster in rivista) (Prodotto della ricerca)
• PATTERN OF PROTEIN EXPRESSIONS IN SURAL NERVE OF CMT1A PATIENTS WITH CHROMOSOME 17p11.2 DUPLICATION (Abstract/Poster in rivista) (Prodotto della ricerca)
• 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 in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• A PET study with [11-C]raclopride in Parkinson's disease: preliminary results on the effect of amantadine on the dopaminergic system. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Screening for PINK1 mutations in patients with early- and late-onset Parkinson disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Association between DJ-1 gene polymorphism and Parkinson disease (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Angiotensin converting enzyme (ACE) gene polymorphism in patients with frontotemporal dementia (FTD) (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Chromatic pattern-reversal electroretinograms (ChPERGs) are spared in Multiple System Atrophy compared with Parkinson’s Disease. (Articolo in rivista) (Prodotto della ricerca)
• Guidelines for the diagnosis of dementia and Alzheimer's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Relevance of pre-hospital stroke-code activation in the acute stroke care: a review. (Abstract in rivista) (Prodotto della ricerca)
• Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case (Abstract in rivista) (Prodotto della ricerca)
• Mutational and linkage analysis in three calabrian families with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Gly2019Ser Mutation in the LRRK2 gene and Parkinson’s disease in the Italian population. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Mutational analysis of EFHC1 gene in southern Italy families with Juvenile Myoclonic Epilepsy.” (Comunicazione a convegno) (Prodotto della ricerca)
• SURAL NERVE PROTEIN PROFILE BY MATRIX ASSISTED LASER DESORPTION IONIZATION-TIME OF FLIGHT MASS SPECTROMETRY (MALDI-TOF MS) DIRECT ANALYSIS: PRELIMINARY DATA. (Abstract/Comunicazione in rivista) (Prodotto della ricerca)
• Chromatic pattern-reversal electroretinograms (ChPERGs) are spared in multiple system atrophy compared with Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Natalizumab is effective in multiple sclerosis patients switching from other disease modifying therapies in clinical practice. (Articolo in rivista) (Prodotto della ricerca)
• Diffusion tensor MRI changes in gray structures of the frontal-subcortical circuits in amyotrophic lateral sclerosis (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Multiple sclerosis in children under 10 years of age (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• 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 (Articolo in rivista) (Prodotto della ricerca)
• MUTATIONAL ANALISYS OF GJB1, MPZ AND PMP22 GENES IN CMT PATIENTS FROM SOUTHERN ITALY (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. (Abstract/Poster in rivista) (Prodotto della ricerca)
• An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Voluntary selective big toe dorsal flection: pseudo-Babinski phenomenon? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Effect of nitric oxide on lymphocytes from sporadic amyotrophic lateral sclerosis patients:toxic or protective role? (Articolo in rivista) (Prodotto della ricerca)

Alternative label

• Neurological sciences. (literal)
• Neurol. sci. (literal)

Language

• eng (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#issn

• 1590-1874 (literal)

Preferred label

• Neurological sciences (literal)

Publisher

• Springer-Verlag Italia Milano : ITA (literal)

Incoming links:

Rivista

• 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 in rivista) (Prodotto della ricerca)
• The end of the central dogma of neurobiology: stem cells and neurogenesis in adult CNS. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses (Articolo in rivista) (Prodotto della ricerca)
• Electrophysiological evidence by single fibre electromyography of neuromuscular impairment in a case of Miller Fisher syndrome. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A PET study with [11-C]raclopride in Parkinson's disease: preliminary results on the effect of amantadine on the dopaminergic system. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Posterior cortical atrophy with prominent alexia without agraphia in a Tourette syndrome (Articolo in rivista) (Prodotto della ricerca)
• Effect of nitric oxide on lymphocytes from sporadic amyotrophic lateral sclerosis patients:toxic or protective role? (Articolo in rivista) (Prodotto della ricerca)
• Chromatic pattern-reversal electroretinograms (ChPERGs) are spared in Multiple System Atrophy compared with Parkinson’s Disease. (Articolo in rivista) (Prodotto della ricerca)
• The status of dopamine nerve terminal in Parkinson’s disease and essential tremor: A PET study with the tracer [11-C]FE-CIT (Articolo in rivista) (Prodotto della ricerca)
• The \"eye of the tiger\" sign in pure akinesia with gait freezing (Articolo in rivista) (Prodotto della ricerca)
• Predictive factors of neutralizing antibodies development in relapsing-remitting multiple sclerosis patients on interferon Beta-1b therapy (Articolo in rivista) (Prodotto della ricerca)
• BDNF Val66Met polymorphism and brain volumes in multiple sclerosis (Articolo in rivista) (Prodotto della ricerca)
• Symptomatic spinal cord metastasis from cerebral oligodendroglioma. (Articolo in rivista) (Prodotto della ricerca)
• 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 in rivista) (Prodotto della ricerca)
• Corpus callosum atrophy is associated with gait disorders in patients with leukoaraiosis. (Articolo in rivista) (Prodotto della ricerca)
• 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). (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Relevance of pre-hospital stroke-code activation in the acute stroke care: a review. (Abstract in rivista) (Prodotto della ricerca)
• Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL): a proteiform neurological disease of expanding importance. Reasons for establishing an Italian Registry. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Treatment of multiple sclerosis with interferon beta in clinical practice: 2-year follow-up data from the South Italy Mobile MRI Project. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Clinical, genetic and magnetic resonance findings in an Italian patient affected by L: -2-hydroxyglutaric aciduria. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• 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 in rivista) (Prodotto della ricerca)
• Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre study. (Articolo in rivista) (Prodotto della ricerca)
• Voluntary selective big toe dorsal flection: pseudo-Babinski phenomenon? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Multiple sclerosis in children under 10 years of age (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Early-onset SCA17 with 43 TBP repeats: expanding the phenotype? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Further insight on A-wave in acute and chronic demyelinating neuropathies. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Prospective study of coffee consumption and risk of Parkinson disease. The Italian Longitudinal Study on Aging. (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Burden and stress among stroke caregivers during the first 2 years after stroke. Results from a community-based study in Italy. (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• The effect of Parkinson's disease and frontal lobe lesions on serial learning (Articolo in rivista) (Prodotto della ricerca)
• Body weight, levodopa pharmacokinetics and dyskinesia in Parkinson's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Non-convulsive status epilepticus during lithium treatment at therapeutic doses (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Expression of multidrug resistance type 1 gene (MDR1) P-glycoprotein in intractable epilepsy with different aetiologies: a double-labelling and electron microscopy study. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Italian studies on early onset multiple sclerosis: the present and the future (Articolo in rivista) (Prodotto della ricerca)
• The FRAGAMP study: environmental and genetic factors in Parkinson's disease, methods and clinical features. (Articolo in rivista) (Prodotto della ricerca)
• Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. (Articolo in rivista) (Prodotto della ricerca)
• 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 in rivista) (Prodotto della ricerca)
• Alzheimer’s disease risk: analysis of the STH and apoE gene polymorphisms (Abstract in rivista) (Prodotto della ricerca)
• Angiotensin converting enzyme (ACE) gene polymorphism in patients with frontotemporal dementia (FTD) (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• 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 in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Screening for PINK1 mutations in patients with early- and late-onset Parkinson disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Association between DJ-1 gene polymorphism and Parkinson disease (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer’s Disease in southern Italy. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• “Parkin mutations in patients with early onset parkinsonism”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• The Tau haplotype contributes to susceptibility to Parkinson’s disease in a Souther Italy population. (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Pink1 mutations and the risk of Parkinson’s disease in family members of Southern Italy (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). (Abstract/Comunicazione in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1106)
• The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis’. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Thymosin beta 4 is overexpressed in Cerebrospinal fluid of Creutzfeldt-Jacob disease patients: a MALDI-TOF MS protein profiling study. (Abstract/Comunicazione in rivista) (Prodotto della ricerca)
• Frequency analysis of autosomal dominant spinocerebellar ataxia (AD-SCA) in the patients from southern Italy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• GIGYF2 (TRNC15) MUTATION ANALYSIS IN PATIENTS WITH FAMILIAL PARKINSON DISEASE WITH AUTOSOMAL-DOMINANT TRANSMISSION (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• A comprehensive mutation analysis of PINK1 gene in South Italy patients with early and late onset Parkinsonism. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• NOTCH3 gene mutations and mtDNA variations (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• BDNF polymorphisms and outcome of post-traumatic vegetative state: results from an italian multicentric study (Abstract in rivista) (Prodotto della ricerca)
• A genetic study on the role of thiamine transporters in a case of atrophic beri-beri (Abstract in rivista) (Prodotto della ricerca)
• Interaction between Apolipoprotein-E4 and traumatic brain injury in patients with Alzheimer?s disease and mild cognitive impairment. (Abstract/Poster in rivista) (Prodotto della ricerca)
• PATTERN OF PROTEIN EXPRESSIONS IN SURAL NERVE OF CMT1A PATIENTS WITH CHROMOSOME 17p11.2 DUPLICATION (Abstract/Poster in rivista) (Prodotto della ricerca)
• SURAL NERVE PROTEIN PROFILE BY MATRIX ASSISTED LASER DESORPTION IONIZATION-TIME OF FLIGHT MASS SPECTROMETRY (MALDI-TOF MS) DIRECT ANALYSIS: PRELIMINARY DATA. (Abstract/Comunicazione in rivista) (Prodotto della ricerca)
• Mutational and linkage analysis in three calabrian families with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Gly2019Ser Mutation in the LRRK2 gene and Parkinson’s disease in the Italian population. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Mutational analysis of EFHC1 gene in southern Italy families with Juvenile Myoclonic Epilepsy.” (Comunicazione a convegno) (Prodotto della ricerca)
• Oxidative stress in Parkinson’s disease: Implication for Glutathione transferase enzyme activity. (Abstract/Poster in rivista) (Prodotto della ricerca)
• Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL (Abstract/Poster in rivista) (Prodotto della ricerca)
• “Linkage and mutational study in two families with Familial Hemiplegic Migraine”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• “Polymorphisms of dopamine D1 and D2 receptor genes influence penetrance in dopa-responsive dystonia”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• “Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Genome wide linkage of a large serbian family with GEFS+. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Clinical and genetic analysis of a four-generation family with autosomal dominant cerebellar ataxia. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• G-463A myeloperoxidase polymorphism and parkinson’s disease (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• DESCRIPTION OF A FOUR-GENERATION FAMILY WITH AUTOSOMAL DOMINANT CEREBELLAR ATAXIA: CLINICAL AND GENETIC ANALYSIS (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• FRAGILE X PREMUTATION ALLELES IN MOVEMENT DISORDERS (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• G-PROTEIN-COUPLED RECEPTOR KINASE 5 AND DEMENTIA IN PARKINSON’S DISEASE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• Gender-related effect of clinical and genetic variables on the cognitive impairment in MS. (Abstract/Poster in rivista) (Prodotto della ricerca)
• APOE-4 allele and disease duration affect verbal memory in mild temporal lobe epilepsy. (Abstract/Poster in rivista) (Prodotto della ricerca)
• Ceruloplasmin gene variations and Parkinson’s disease: an association study in Southern Italian population. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• The minor Alois Alzheimer before the discovery of the eponymous disorder (Abstract/Comunicazione in rivista) (Prodotto della ricerca)
• Colour vision in patients with Parkinson disease. Usefulness of three pseudoisochromatic tests (Abstract/Comunicazione in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1106)
• CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. (Abstract/Poster in rivista) (Prodotto della ricerca)
• MALDI-TOF-MS peptide patterns in cerebrospinal fluid from patients withy idiopathic intracranial hypertension. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• “Mutational analysis of SCN2A gene in italian families with benign familial neonatal-infantile seizures (BFNIS)”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• “Clinic and genetic study in a family with a clinical picture of pantothenase kinase-associated neurodegeneration”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• “Alpha-synuclein promoter haplotypes and dementia in Parkinson’s disease”. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Parkin mutations analysis in patients with sporadic early-onset Parkinson’s disease (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• DJ-1 gene confers susceptibility to Parkinson’s disease. (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Glucocerebrosidase gene mutations are associated with Parkinson’s disease in a population from Souther Italy. (Comunicazione a convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1303)
• Sca17 as cause of early-onset dementia in sothern Italy: report of a new family. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Alpha synuclein in familial parkinson’s disease and lewy body dementia. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• A patient with Frontotemporal Dementia (FTD) and Motor Neuron Disease (MND) carrying the intron10+29 substitution in MAPT (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Mutational screening of the CAPN3 in LGMD patients from Southern Italy. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• GENETIC STUDY OF SCN1A-RELATED EPILEPSIES IN SOUTHERN ITALY (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• IDENTIFICATION OF A NOVEL HOMOZYGOUS MUTATION IN THE SIL1 GENE IN MARINESCO-SJOGREN SYNDROME (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• ASSOCIATION STUDY BETWEEN HFE, TF , TFR1 GENES AND PARKINSON’S DISEASE (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• PARKIN, PINK1 AND DJ-1 HETEROZYGOUS MUTATIONS IN SOUTHERN ITALIAN PATIENTS WITH EARLY-ONSET PARKINSONISM (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• MUTATIONAL DETECTION OF EARLY ONSET PARKINSON DISEASE GENES IN PATIENTS FROM SOUTHERN ITALY (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• MTDNA HAPLOGROUP K IS PROTECTIVE AGAINST PD IN ITALIAN POPULATION (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• CASP-9: a susceptibility locus for multiple sclerosis in Italy. (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• ADULT ONSET TAY-SACHS ASSOCIATED WITH ’-HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
• Vitamins prevent the neurological symptoms in their deficiency disorders (Abstract/Comunicazione in rivista) (Prodotto della ricerca)
• 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/Comunicazione in rivista) (Prodotto della ricerca)
• Vascular factors predict polyneuropathy in a non-diabetic elderly population. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Currently used implementation methods in the area of stroke care and stroke prevention in Europe. The European Implementation Score (EIS) Project. (Abstract in rivista) (Prodotto della ricerca)
• Updating on Italian Stroke Units: the \"CCM Study\" (Articolo in rivista) (Prodotto della ricerca)
• Association study of NACP-REP1 polymorphism and Parkinson's disease (Abstract in rivista) (Prodotto della ricerca)
• Analytic information processing style in migraineurs (Articolo in rivista) (Prodotto della ricerca)
• VLA-4 and Multiple Sclerosis in Italian population. (Abstract/Poster in rivista) (Prodotto della ricerca)
• Chromatic pattern-reversal electroretinograms (ChPERGs) are spared in multiple system atrophy compared with Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Natalizumab is effective in multiple sclerosis patients switching from other disease modifying therapies in clinical practice. (Articolo in rivista) (Prodotto della ricerca)
• Contribution of TARDBP mutations to Amyotrophic Lateral Sclerosis. (Abstract in rivista) (Prodotto della ricerca)
• A large Italian family with R521C mutation in the FUS/TLS gene (Abstract/Poster in rivista) (Prodotto della ricerca)
• Could Mitochondrial Haplogroups Play A Role In Sporadic Amyotrophic Lateral Sclerosis? (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Functional Cortical Changes In Amyotrophic Lateral Sclerosis: An FMRI Study In The Early Stage Of The Disease (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• 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 (Articolo in rivista) (Prodotto della ricerca)
• Polymorphism Ile587val in the eIF2B5 gene as susceptibility factor in multiple sclerosis (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Autosomal Dominant Distal Motor Neuropathy: an Italian family not linked to known loci (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Clinical and genetic study of an Italian family linked to SPG26 locus (Abstract in rivista) (Prodotto della ricerca)
• Subcortical Motor Plasticity In Patients With Sporadic Amyotrophic Lateral Sclerosis (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Diffusion tensor MRI changes in gray structures of the frontal-subcortical circuits in amyotrophic lateral sclerosis (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Position paper of the Italian Society for the study of Dementias (Sindem) on the proposal of a new Lexicon on Alzheimer disease (Articolo in rivista) (Prodotto della ricerca)
• 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 (Articolo in rivista) (Prodotto della ricerca)
• A NOVEL MUTATION IN CX32 IDENTIFIED IN A PATIENT WITH DEMYELINATING SENSORY-MOTOR NEUROPATHY AND SECONDARY AXONOPATHY (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• A novel mutation in the exon 7 of the NOTCH3 gene in a patient affected by CADASIL (Abstract in rivista) (Prodotto della ricerca)
• Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations (Abstract in rivista) (Prodotto della ricerca)
• Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• NOTCH3 PROTEIN LOCALIZATION IN SKIN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE MICROSCOPY STUDY (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Italian multicentre observational study of the prevalence of CCSVI in multiple sclerosis (CoSMo study): Rationale, design, and methodology (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case (Abstract in rivista) (Prodotto della ricerca)
• Clinical, genetic and magnetic resonance findings in an Italian patient affected by l-2-hydroxyglutaric aciduria (Articolo in rivista) (Prodotto della ricerca)
• \"Identification and functional characterization of novel alleles in the promoter region of the serotonin transporter gene\" (Abstract in rivista) (Prodotto della ricerca)
• Autosomal dominant essential tremor: A novel family with anticipation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• 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 in rivista) (Prodotto della ricerca)
• Italian Neurological Society guidelines for the diagnosis of dementia: revision I (Articolo in rivista) (Prodotto della ricerca)
• MUTATIONAL ANALISYS OF GJB1, MPZ AND PMP22 GENES IN CMT PATIENTS FROM SOUTHERN ITALY (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• An intronic nucleotide change in the SPAST gene might produce an aberrant protein transcript (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• SPORADIC ALS AND VCP GENE ANALISYS IN SOUTHERN ITALY (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• Amiotrophic Lateral Sclerosis: a new missense mutation in SOD1 gene (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• An Italian child with myophosphorylase deficiency but with no detectable mutation in the exons of the PYGM gene (Abstract/Poster in rivista) (Prodotto della ricerca)
• Brown-Vialetto-Van Laere Syndrome: a case report of a family from Italy (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)
• GENETIC COUNSELLING IN ALS: FACTS, UNCERTAINTIES AND RECOMMENDATIONS (Abstract in rivista) (Prodotto della ricerca)
• Guidelines for the diagnosis of dementia and Alzheimer's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Lack of association between GRIN2B gene coding for 2B subunit of the NMDA receptor and Alzheimer's disease (Abstract in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1105)