Journal of neurology

Label

• Journal of neurology (literal)

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

• Poor metabolization of n-hexane in Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD) (Articolo in rivista) (Prodotto della ricerca)
• Dopamine transporter availability in motor subtypes of de novo drug-naive Parkinson's disease (Articolo in rivista) (Prodotto della ricerca)
• Gender-related differences in the electrical activity of the subthalamic nucleus: a local field potentials study in Parkinson's disease (Articolo in rivista) (Prodotto della ricerca)
• Comparison of different MR venography techniques for detecting transverse sinus stenosis in idiopathic intracranial hypertension. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Dopaminergic pathways involvement in Kennedy's disease: Neuropsychological and [123I] ß-CIT SPECT findings. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Intracranial pressure in unresponsive chronic migraine (Articolo in rivista) (Prodotto della ricerca)
• A Phase II Randomized Controlled Clinical Trial of Lithium in Spinocerebellar Ataxia Type 2 (Articolo in rivista) (Prodotto della ricerca)
• Nigrostriatal involvement in ataxia with oculomotor apraxia type 1 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Cerebellar metabolic involvement and its correlations with clinical parameters in vestibular neuritis (Articolo in rivista) (Prodotto della ricerca)
• Brain SPECT in subtypes of mild cognitive impairment : Findings from the DESCRIPA multicenter study. (Articolo in rivista) (Prodotto della ricerca)
• Familial mesial temporal lobe epilepsy (FMTLE): a clinical and genetic study of 15 Italian families. (Articolo in rivista) (Prodotto della ricerca)
• A randomized clinical trial of lithium in multiple system atrophy (Articolo in rivista) (Prodotto della ricerca)
• Phenotype variability of dystonia in monozygotic twins. (Articolo in rivista) (Prodotto della ricerca)
• Phenotypic heterogeneity of Niemann-Pick disease type C in monozygotic twins (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Hyperhomocysteinemia is associated with cognitive impairment in multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
• Cerebral metabolic correlates of four dementia scales in Alzheimer's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Pre-clinical diagnosis of Alzheimer disease combining platelet amyloid precursor protein ratio and rCBF SPECT analysis (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A randomized controlled clinical trial of growth hormone in amyotrophic lateral sclerosis: clinical, neuroimaging, and hormonal results. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• News from epidemiological studies on Alzheimer's and Parkinson's disease: a personal perspective (Articolo in rivista) (Prodotto della ricerca)
• A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. (Articolo in rivista) (Prodotto della ricerca)
• A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. (Articolo in rivista) (Prodotto della ricerca)
• Levodopa reduces risk factors for vascular disease in parkinsonian patients. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Predictors of progression of cognitive decline in Alzheimer's disease: the role of vascular and sociodemographic factors (Articolo in rivista) (Prodotto della ricerca)
• A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension (Articolo in rivista) (Prodotto della ricerca)
• Complex phenotype in an Italian family with a novel mutation in SPG3A (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Complex phenotype in an Italian family with novel mutation in SPG3A (Abstract in rivista) (Prodotto della ricerca)
• Bilateral transverse sinus stenosis and idiopathic intracranial hypertension without papilledema in chronic tension-type headache. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Apolipoprotein E genotype does not influence the progression of multiple sclerosis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Empty sella and bilateral transverse sinus stenosis predict raised intracranial pressure in the absence of papilloedema: a preliminary study. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity. (Articolo in rivista) (Prodotto della ricerca)
• Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• : Posture-related cough headache and orthostatic drop in lumbar CSF pressure. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Outcome prediction in acute monohemispheric stroke via magnetoencephalography (Articolo in rivista) (Prodotto della ricerca)
• A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation (Articolo in rivista) (Prodotto della ricerca)
• Functional and structural balances of homologous sensorimotor regions in multiple sclerosis fatigue (Articolo in rivista) (Prodotto della ricerca)
• Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
• Gender-related effect of clinical and genetic variables on the cognitive impairment in multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
• A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3 (Articolo in rivista) (Prodotto della ricerca)
• A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis (Articolo in rivista) (Prodotto della ricerca)
• Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy (Abstract/Comunicazione in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1305)
• MR imaging and cognitive correlates of relapsing-remitting multiple sclerosis patients with cerebellar symptoms. (Articolo in rivista) (Prodotto della ricerca)

Alternative label

• Journal of neurology. (literal)
• J. neurol. (literal)
• Zeitschrift für Neurologie (1974) (literal)

Language

• mul (literal)

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

• 0340-5354 (literal)

Preferred label

• Journal of neurology (literal)

Publisher

• Springer-Medizin-Verl. Heidelberg : DEU (literal)

Incoming links:

Rivista

• Phenotype variability of dystonia in monozygotic twins. (Articolo in rivista) (Prodotto della ricerca)
• Complex phenotype in an Italian family with a novel mutation in SPG3A (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Pre-clinical diagnosis of Alzheimer disease combining platelet amyloid precursor protein ratio and rCBF SPECT analysis (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Cerebral metabolic correlates of four dementia scales in Alzheimer's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Brain SPECT in subtypes of mild cognitive impairment : Findings from the DESCRIPA multicenter study. (Articolo in rivista) (Prodotto della ricerca)
• Gender-related differences in the electrical activity of the subthalamic nucleus: a local field potentials study in Parkinson's disease (Articolo in rivista) (Prodotto della ricerca)
• Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Dopaminergic pathways involvement in Kennedy's disease: Neuropsychological and [123I] ß-CIT SPECT findings. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Nigrostriatal involvement in ataxia with oculomotor apraxia type 1 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A randomized controlled clinical trial of growth hormone in amyotrophic lateral sclerosis: clinical, neuroimaging, and hormonal results. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Apolipoprotein E genotype does not influence the progression of multiple sclerosis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Hyperhomocysteinemia is associated with cognitive impairment in multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
• A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. (Articolo in rivista) (Prodotto della ricerca)
• Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
• Gender-related effect of clinical and genetic variables on the cognitive impairment in multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
• Bilateral transverse sinus stenosis and idiopathic intracranial hypertension without papilledema in chronic tension-type headache. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• : Posture-related cough headache and orthostatic drop in lumbar CSF pressure. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Outcome prediction in acute monohemispheric stroke via magnetoencephalography (Articolo in rivista) (Prodotto della ricerca)
• A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3 (Articolo in rivista) (Prodotto della ricerca)
• A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis (Articolo in rivista) (Prodotto della ricerca)
• Comparison of different MR venography techniques for detecting transverse sinus stenosis in idiopathic intracranial hypertension. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Empty sella and bilateral transverse sinus stenosis predict raised intracranial pressure in the absence of papilloedema: a preliminary study. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Poor metabolization of n-hexane in Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Levodopa reduces risk factors for vascular disease in parkinsonian patients. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Complex phenotype in an Italian family with novel mutation in SPG3A (Abstract in rivista) (Prodotto della ricerca)
• Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy (Abstract/Comunicazione in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1305)
• Familial mesial temporal lobe epilepsy (FMTLE): a clinical and genetic study of 15 Italian families. (Articolo in rivista) (Prodotto della ricerca)
• MR imaging and cognitive correlates of relapsing-remitting multiple sclerosis patients with cerebellar symptoms. (Articolo in rivista) (Prodotto della ricerca)
• Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A randomized clinical trial of lithium in multiple system atrophy (Articolo in rivista) (Prodotto della ricerca)
• CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity. (Articolo in rivista) (Prodotto della ricerca)
• A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. (Articolo in rivista) (Prodotto della ricerca)
• Phenotypic heterogeneity of Niemann-Pick disease type C in monozygotic twins (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation (Articolo in rivista) (Prodotto della ricerca)
• A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension (Articolo in rivista) (Prodotto della ricerca)
• News from epidemiological studies on Alzheimer's and Parkinson's disease: a personal perspective (Articolo in rivista) (Prodotto della ricerca)
• Predictors of progression of cognitive decline in Alzheimer's disease: the role of vascular and sociodemographic factors (Articolo in rivista) (Prodotto della ricerca)
• Functional and structural balances of homologous sensorimotor regions in multiple sclerosis fatigue (Articolo in rivista) (Prodotto della ricerca)
• A Phase II Randomized Controlled Clinical Trial of Lithium in Spinocerebellar Ataxia Type 2 (Articolo in rivista) (Prodotto della ricerca)
• Intracranial pressure in unresponsive chronic migraine (Articolo in rivista) (Prodotto della ricerca)
• Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD) (Articolo in rivista) (Prodotto della ricerca)
• Dopamine transporter availability in motor subtypes of de novo drug-naive Parkinson's disease (Articolo in rivista) (Prodotto della ricerca)
• Cerebellar metabolic involvement and its correlations with clinical parameters in vestibular neuritis (Articolo in rivista) (Prodotto della ricerca)