Journal of the neurological sciences

Label

• Journal of the neurological sciences (literal)

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

• Newly characterized 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine or episodic Ataxia type 2 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in anoctogenarian paucisymptomatic patient. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary chorea (Articolo in rivista) (Prodotto della ricerca)
• Oxidative stress, mitochondrial dysfunction and cellular stress response in Friedreich's ataxia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Early onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop (Articolo in rivista) (Prodotto della ricerca)
• A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• AUTOSOMAL DOMINANT BROWN-VIALETTO-VAN LAERE SYNDROME WITH UBQLN1 MUTATION (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Selective risk factors profiles and outcomes among patients with stroke and history of prior myocardial infarction (Articolo in rivista) (Prodotto della ricerca)
• Correlation between fatigue and brain atrophy and lesion load in multiple sclerosis patients independent of disability. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary chorea (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• Reply to (Articolo in rivista) (Prodotto della ricerca)
• Charcot-Marie-Tooth and pain: correlations with neurophysiological, clinical, and disability findings. (Articolo in rivista) (Prodotto della ricerca)
• Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia. (Articolo in rivista) (Prodotto della ricerca)
• Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. (Articolo in rivista) (Prodotto della ricerca)
• Tongue's motor evoked potentials in the diagnosis of Primary Lateral Sclerosis (PLS): Preliminary report. (Articolo in rivista) (Prodotto della ricerca)
• White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: characterization by MRI (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Dramatically different levels of cacna1a gene expression between pre-weaning wild type and leaner mice. (Articolo in rivista) (Prodotto della ricerca)
• Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation (Articolo in rivista) (Prodotto della ricerca)
• Spontaneous obliteration of MRI-silent cerebral angiomatosis revealed by CT angiography in a patient with Sturge-Weber syndrome. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population. (Articolo in rivista) (Prodotto della ricerca)
• Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• DNA-REPAIR MECHANISMS IN NEUROLOGICAL DISEASES - FACTS AND HYPOTHESES (Articolo in rivista) (Prodotto della ricerca)
• Risk factors and outcome of subtypes of ischemic stroke. Data from a multicenter multinational hospital-based registry. The European Community Stroke Project. (Articolo in rivista) (Prodotto della ricerca)
• White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: Characterization by MRI (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Neuropsychological assessment, quantitative MRI and ApoE gene polymorphismsin a series of MS patients treated with IFN beta-1b (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Atypical clinical and radiological presentation of cryptococcal choroid plexitis in an immunocompetent woman (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Predictors of non-invasive ventilation tolerance in amyotrophic lateral sclerosis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Somatosensory evoked potentials reflect the upper limb motor performance in multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
• NOS2A as a candidate gene in Relapsing-Remitting Multiple Sclerosis: a haplotype study using selected subsets of single nucleotide polymorphisms. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: Further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population. (Articolo in rivista) (Prodotto della ricerca)

Alternative label

• J. neurol. sci. (literal)
• Journal of neurological science (literal)

Language

• mul (literal)

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

• 0022-510X (literal)

Preferred label

• Journal of the neurological sciences (literal)

Publisher

• Elsevier New York ; NLD (literal)

Incoming links:

Rivista

• Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary chorea (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary chorea (Articolo in rivista) (Prodotto della ricerca)
• Early onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop (Articolo in rivista) (Prodotto della ricerca)
• Predictors of non-invasive ventilation tolerance in amyotrophic lateral sclerosis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Neuropsychological assessment, quantitative MRI and ApoE gene polymorphismsin a series of MS patients treated with IFN beta-1b (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Selective risk factors profiles and outcomes among patients with stroke and history of prior myocardial infarction (Articolo in rivista) (Prodotto della ricerca)
• A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in anoctogenarian paucisymptomatic patient. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Newly characterized 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine or episodic Ataxia type 2 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Risk factors and outcome of subtypes of ischemic stroke. Data from a multicenter multinational hospital-based registry. The European Community Stroke Project. (Articolo in rivista) (Prodotto della ricerca)
• A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Reply to (Articolo in rivista) (Prodotto della ricerca)
• Charcot-Marie-Tooth and pain: correlations with neurophysiological, clinical, and disability findings. (Articolo in rivista) (Prodotto della ricerca)
• Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. (Articolo in rivista) (Prodotto della ricerca)
• Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia. (Articolo in rivista) (Prodotto della ricerca)
• Dramatically different levels of cacna1a gene expression between pre-weaning wild type and leaner mice. (Articolo in rivista) (Prodotto della ricerca)
• Spontaneous obliteration of MRI-silent cerebral angiomatosis revealed by CT angiography in a patient with Sturge-Weber syndrome. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population. (Articolo in rivista) (Prodotto della ricerca)
• White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: characterization by MRI (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Somatosensory evoked potentials reflect the upper limb motor performance in multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
• Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: Further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population. (Articolo in rivista) (Prodotto della ricerca)
• Oxidative stress, mitochondrial dysfunction and cellular stress response in Friedreich's ataxia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• NOS2A as a candidate gene in Relapsing-Remitting Multiple Sclerosis: a haplotype study using selected subsets of single nucleotide polymorphisms. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation (Articolo in rivista) (Prodotto della ricerca)
• Tongue's motor evoked potentials in the diagnosis of Primary Lateral Sclerosis (PLS): Preliminary report. (Articolo in rivista) (Prodotto della ricerca)
• Correlation between fatigue and brain atrophy and lesion load in multiple sclerosis patients independent of disability. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• AUTOSOMAL DOMINANT BROWN-VIALETTO-VAN LAERE SYNDROME WITH UBQLN1 MUTATION (Abstract/Poster in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1107)
• Atypical clinical and radiological presentation of cryptococcal choroid plexitis in an immunocompetent woman (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: Characterization by MRI (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• DNA-REPAIR MECHANISMS IN NEUROLOGICAL DISEASES - FACTS AND HYPOTHESES (Articolo in rivista) (Prodotto della ricerca)