http://www.cnr.it/ontology/cnr/individuo/rivista/ID294452
Neurology
- Label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
- A familial form of multiple sclerosis showing impaired ganglioside synthesis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers (Articolo in rivista) (Prodotto della ricerca)
- Regional reductions of gray matter volume in familial dyslexia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Vitamin D deficiency predicts cognitive decline in older men and women The Pro.VA Study (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Intraventricular tumor presenting as progressive supranuclear palsy-like phenotype (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Left caloric vestibular stimulation ameliorates right hemianesthesia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Effects of Bacille Calmette-Guérin after the first demyelinating event in the CNS (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The parkin gene is not involved in late-onset Parkinson's disease (Articolo in rivista) (Prodotto della ricerca)
- A proposed dual role of neuromelanin in the pathogenesis of Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease. (Articolo in rivista) (Prodotto della ricerca)
- Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity. (Articolo in rivista) (Prodotto della ricerca)
- Neuropsychological assessment in children with absence epilepsy (Articolo in rivista) (Prodotto della ricerca)
- Cerebral MR venography of transverse sinuses in subjects with normal CSF pressure. (Articolo in rivista) (Prodotto della ricerca)
- Juvenile Huntington's disease presenting as progressive myoclonic epilepsy. (Articolo in rivista) (Prodotto della ricerca)
- Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy. (Articolo in rivista) (Prodotto della ricerca)
- Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation. (Articolo in rivista) (Prodotto della ricerca)
- A novel mutation in SACS gene in a family from southern Italy (Articolo in rivista) (Prodotto della ricerca)
- Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype. (Articolo in rivista) (Prodotto della ricerca)
- Conventional MRI and NOTCH3 gene screening in sporadic CADASIL. (Articolo in rivista) (Prodotto della ricerca)
- Sex differences in presentation, severity, and management of stroke in (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study (Articolo in rivista) (Prodotto della ricerca)
- Diffusion tensor MRI changes in cerebellar structures of patients with familial essential tremor. (Articolo in rivista) (Prodotto della ricerca)
- The differential effect of PD and normal aging on early explicit sequence learning (Articolo in rivista) (Prodotto della ricerca)
- Alcohol consumption, mild cognitive impairment, and progression to dementia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum. (Articolo in rivista) (Prodotto della ricerca)
- Hippocampal and Thalamic Atrophy in Pharmaco-Sensitive Temporal Lobe Epilepsy: a VBM study (Articolo in rivista) (Prodotto della ricerca)
- Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Inverse occurrence of cancer and Alzheimer disease A population-based incidence study (Articolo in rivista) (Prodotto della ricerca)
- CSF opening pressure: reference interval and the effect of body mass index (Articolo in rivista) (Prodotto della ricerca)
- MRI evidence of mesial temporal sclerosis in sporadic \"benign\" temporal lobe epilepsy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Bilateral transverse sinus stenosis predicts IIH without papilledema in patients with migraine (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Motor sensory neuropathy with minifascicle formation in a woman with normal karyotype (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P) (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Riluzole in cerebellar ataxia: a randomized, double-blind, placebo-controlled pilot trial (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. (Articolo in rivista) (Prodotto della ricerca)
- GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. (Articolo in rivista) (Prodotto della ricerca)
- Transverse sinus stenoses persist after normalization of the CSF pressure in IIH (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH. (Articolo in rivista) (Prodotto della ricerca)
- Treatment of first tonic-clonic seizure does not improve the prognosis of epilepsy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Obesity does not induce abnormal CSF pressure in subjects with normal cerebral MR venography. (Articolo in rivista) (Prodotto della ricerca)
- Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Association study of dopamine D2, D3 receptor gene polymorphisms with motor fluctuations in PD (Articolo in rivista) (Prodotto della ricerca)
- Blink reflex recovery cycle in patients with essential tremor associated with resting tremor. (Articolo in rivista) (Prodotto della ricerca)
- Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Manometry combined with cervical puncture in idiopathic intracranial hypertension (Articolo in rivista) (Prodotto della ricerca)
- Neurophysiological correlates of age-related changes in human motor function (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Autosomal recessive Bethlem myopathy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Association of gait and balance disorders with age-related white matter changes: the LADIS study. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Autosomal recessive myosclerosis myopathy is a collagen VI disorder. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Education and occupation as proxies for reserve in aMCI converters and AD: FDG-PET evidence. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Phenotypic clustering of lamin A/C mutations in neuromuscular patients. (Articolo in rivista) (Prodotto della ricerca)
- Brain atrophy and lesion load in a large population of patients with multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
- A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Blink reflex recovery cycle in patients with dystonic tremor: a cross-sectional study (Articolo in rivista) (Prodotto della ricerca)
- Fixed dystonia unresponsive to pallidal stimulation improved by motor cortex stimulation. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Brain metabolic differences between sporadic and familial Alzheimer's disease. (Articolo in rivista) (Prodotto della ricerca)
- Brain atrophy and lesion load in a large population of patients with multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
- Adenosine A2A and dopamine receptor interactions in basal ganglia of dopamine denervated rats. (Articolo in rivista) (Prodotto della ricerca)
- COHORT study of the HSG. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion (Articolo in rivista) (Prodotto della ricerca)
- MRI measurements predict PSP in unclassifiable parkinsonisms: a follow-up study (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Course and prognosis in early-onset MS: comparison with adult-onset forms. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Worldwide distribution of PSEN1 Met146Leu mutation A large variability for a founder mutation (Articolo in rivista) (Prodotto della ricerca)
- European Registers of Stroke. Three-month stroke outcome: the European Registers of Stroke (EROS) investigators (Articolo in rivista) (Prodotto della ricerca)
- Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. (Articolo in rivista) (Prodotto della ricerca)
- Cysteine-sparing notch3 mutations: cadasil or cadasil variants? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- HLA B*44: protective effects in MS susceptibility and MRI outcome measures (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2). (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- IV amantadine improves chorea in Huntington's disease: an acute randomized, controlled study (Articolo in rivista) (Prodotto della ricerca)
- Amygdala dysplasia with temporal lobe epilepsy and obsessive-compulsive disorder: an fMRI/EEG study (Articolo in rivista) (Prodotto della ricerca)
- White matter changes and diabetes predict cognitive decline in the elderly: the LADIS study. (Articolo in rivista) (Prodotto della ricerca)
- Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy. (Articolo in rivista) (Prodotto della ricerca)
- The fragile X premutation presenting as postprandial hypotension. (Articolo in rivista) (Prodotto della ricerca)
- LMNA-associated myopathies: The Italian experience in a large cohort of patients. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Epidemiology of distal symmetrical neuropathies in the Italian elderly. (Articolo in rivista) (Prodotto della ricerca)
- CIND and MCI in the Italian elderly: frequency, vascular risk factors, progression to dementia. (Articolo in rivista) (Prodotto della ricerca)
- CASES Investigators. Leukoaraiosis and intracerebral hemorrhage after thrombolysis in acute stroke. (Articolo in rivista) (Prodotto della ricerca)
- Alzheimer disease risk associated with APOE4 is modified by STH gene polymorphism (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL. (Articolo in rivista) (Prodotto della ricerca)
- The midbrain to pons ratio: A simple and specific MRI sign of progressive supranuclear palsy. (Articolo in rivista) (Prodotto della ricerca)
- Two Novel CYP7131 Mutations in Italian Families with Autosomal Recessive Spastic Paraplegia: A Clinical and Genetic Study (Abstract in rivista) (Prodotto della ricerca)
- MCI conversion to dementia and the APOE genotype: a prediction study with FDG-PET (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Mild cognitive impairment in drug-naive patients with PD is associated with cerebral hypometabolism (Articolo in rivista) (Prodotto della ricerca)
- Teaching NeuroImages: pseudo-abnormal DaTscan findings in meningioma-induced parkinsonism. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- LGI1 microdeletion in autosomal dominant lateral temporal epilepsy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Limited chronic focal encephalitis: another variant of Rasmussen syndrome? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Does lamotrigine use in pregnancy increase orofacial cleft risk relative to other malformations? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The association of chronic hepatitis B and myopathy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Alternative label
- Neurology. (literal)
- Neurology (literal)
- Language
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#issn
- Preferred label
- Publisher
- Advanstar Communications [etc.] Cleveland, Ohio [etc.] USA (literal)
Incoming links:
- Rivista
- Alzheimer disease risk associated with APOE4 is modified by STH gene polymorphism (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The differential effect of PD and normal aging on early explicit sequence learning (Articolo in rivista) (Prodotto della ricerca)
- Fixed dystonia unresponsive to pallidal stimulation improved by motor cortex stimulation. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Education and occupation as proxies for reserve in aMCI converters and AD: FDG-PET evidence. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Worldwide distribution of PSEN1 Met146Leu mutation A large variability for a founder mutation (Articolo in rivista) (Prodotto della ricerca)
- Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Does lamotrigine use in pregnancy increase orofacial cleft risk relative to other malformations? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. (Articolo in rivista) (Prodotto della ricerca)
- The association of chronic hepatitis B and myopathy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Left caloric vestibular stimulation ameliorates right hemianesthesia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Regional reductions of gray matter volume in familial dyslexia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A familial form of multiple sclerosis showing impaired ganglioside synthesis. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- IV amantadine improves chorea in Huntington's disease: an acute randomized, controlled study (Articolo in rivista) (Prodotto della ricerca)
- Epidemiology of distal symmetrical neuropathies in the Italian elderly. (Articolo in rivista) (Prodotto della ricerca)
- CIND and MCI in the Italian elderly: frequency, vascular risk factors, progression to dementia. (Articolo in rivista) (Prodotto della ricerca)
- CASES Investigators. Leukoaraiosis and intracerebral hemorrhage after thrombolysis in acute stroke. (Articolo in rivista) (Prodotto della ricerca)
- Sex differences in presentation, severity, and management of stroke in (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- MCI conversion to dementia and the APOE genotype: a prediction study with FDG-PET (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Mild cognitive impairment in drug-naive patients with PD is associated with cerebral hypometabolism (Articolo in rivista) (Prodotto della ricerca)
- A novel mutation in SACS gene in a family from southern Italy (Articolo in rivista) (Prodotto della ricerca)
- Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype. (Articolo in rivista) (Prodotto della ricerca)
- Phenotypic clustering of lamin A/C mutations in neuromuscular patients. (Articolo in rivista) (Prodotto della ricerca)
- Autosomal recessive myosclerosis myopathy is a collagen VI disorder. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Autosomal recessive Bethlem myopathy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Brain metabolic differences between sporadic and familial Alzheimer's disease. (Articolo in rivista) (Prodotto della ricerca)
- Adenosine A2A and dopamine receptor interactions in basal ganglia of dopamine denervated rats. (Articolo in rivista) (Prodotto della ricerca)
- Alcohol consumption, mild cognitive impairment, and progression to dementia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1 (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Association of gait and balance disorders with age-related white matter changes: the LADIS study. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- White matter changes and diabetes predict cognitive decline in the elderly: the LADIS study. (Articolo in rivista) (Prodotto della ricerca)
- European Registers of Stroke. Three-month stroke outcome: the European Registers of Stroke (EROS) investigators (Articolo in rivista) (Prodotto della ricerca)
- Association study of dopamine D2, D3 receptor gene polymorphisms with motor fluctuations in PD (Articolo in rivista) (Prodotto della ricerca)
- Manometry combined with cervical puncture in idiopathic intracranial hypertension (Articolo in rivista) (Prodotto della ricerca)
- GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. (Articolo in rivista) (Prodotto della ricerca)
- Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH. (Articolo in rivista) (Prodotto della ricerca)
- Obesity does not induce abnormal CSF pressure in subjects with normal cerebral MR venography. (Articolo in rivista) (Prodotto della ricerca)
- Motor sensory neuropathy with minifascicle formation in a woman with normal karyotype (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- MRI evidence of mesial temporal sclerosis in sporadic \"benign\" temporal lobe epilepsy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The fragile X premutation presenting as postprandial hypotension. (Articolo in rivista) (Prodotto della ricerca)
- A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2). (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Cysteine-sparing notch3 mutations: cadasil or cadasil variants? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- HLA B*44: protective effects in MS susceptibility and MRI outcome measures (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- MRI measurements predict PSP in unclassifiable parkinsonisms: a follow-up study (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Course and prognosis in early-onset MS: comparison with adult-onset forms. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Blink reflex recovery cycle in patients with dystonic tremor: a cross-sectional study (Articolo in rivista) (Prodotto della ricerca)
- Cerebral MR venography of transverse sinuses in subjects with normal CSF pressure. (Articolo in rivista) (Prodotto della ricerca)
- Juvenile Huntington's disease presenting as progressive myoclonic epilepsy. (Articolo in rivista) (Prodotto della ricerca)
- Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy. (Articolo in rivista) (Prodotto della ricerca)
- The parkin gene is not involved in late-onset Parkinson's disease (Articolo in rivista) (Prodotto della ricerca)
- Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease. (Articolo in rivista) (Prodotto della ricerca)
- Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity. (Articolo in rivista) (Prodotto della ricerca)
- APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers (Articolo in rivista) (Prodotto della ricerca)
- Limited chronic focal encephalitis: another variant of Rasmussen syndrome? (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Conventional MRI and NOTCH3 gene screening in sporadic CADASIL. (Articolo in rivista) (Prodotto della ricerca)
- Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study (Articolo in rivista) (Prodotto della ricerca)
- Diffusion tensor MRI changes in cerebellar structures of patients with familial essential tremor. (Articolo in rivista) (Prodotto della ricerca)
- Neurophysiological correlates of age-related changes in human motor function (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P) (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Transverse sinus stenoses persist after normalization of the CSF pressure in IIH (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Bilateral transverse sinus stenosis predicts IIH without papilledema in patients with migraine (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- CSF opening pressure: reference interval and the effect of body mass index (Articolo in rivista) (Prodotto della ricerca)
- Hippocampal and Thalamic Atrophy in Pharmaco-Sensitive Temporal Lobe Epilepsy: a VBM study (Articolo in rivista) (Prodotto della ricerca)
- Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum. (Articolo in rivista) (Prodotto della ricerca)
- Amygdala dysplasia with temporal lobe epilepsy and obsessive-compulsive disorder: an fMRI/EEG study (Articolo in rivista) (Prodotto della ricerca)
- Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy. (Articolo in rivista) (Prodotto della ricerca)
- Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. (Articolo in rivista) (Prodotto della ricerca)
- A proposed dual role of neuromelanin in the pathogenesis of Parkinson's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Two Novel CYP7131 Mutations in Italian Families with Autosomal Recessive Spastic Paraplegia: A Clinical and Genetic Study (Abstract in rivista) (Prodotto della ricerca)
- Brain atrophy and lesion load in a large population of patients with multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
- Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Brain atrophy and lesion load in a large population of patients with multiple sclerosis. (Articolo in rivista) (Prodotto della ricerca)
- COHORT study of the HSG. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion (Articolo in rivista) (Prodotto della ricerca)
- Riluzole in cerebellar ataxia: a randomized, double-blind, placebo-controlled pilot trial (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL. (Articolo in rivista) (Prodotto della ricerca)
- Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation. (Articolo in rivista) (Prodotto della ricerca)
- Blink reflex recovery cycle in patients with essential tremor associated with resting tremor. (Articolo in rivista) (Prodotto della ricerca)
- Teaching NeuroImages: pseudo-abnormal DaTscan findings in meningioma-induced parkinsonism. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The midbrain to pons ratio: A simple and specific MRI sign of progressive supranuclear palsy. (Articolo in rivista) (Prodotto della ricerca)
- Effects of Bacille Calmette-Guérin after the first demyelinating event in the CNS (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Intraventricular tumor presenting as progressive supranuclear palsy-like phenotype (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Treatment of first tonic-clonic seizure does not improve the prognosis of epilepsy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Inverse occurrence of cancer and Alzheimer disease A population-based incidence study (Articolo in rivista) (Prodotto della ricerca)
- Neuropsychological assessment in children with absence epilepsy (Articolo in rivista) (Prodotto della ricerca)
- LMNA-associated myopathies: The Italian experience in a large cohort of patients. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- LGI1 microdeletion in autosomal dominant lateral temporal epilepsy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Vitamin D deficiency predicts cognitive decline in older men and women The Pro.VA Study (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)