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NEUROLOGICAL SCIENCES (ONLINE)
Rivista
Codice:
E117263
ISSN:
1590-3478
Dati Generali
Dati Generali
Pubblicazioni (39)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
A NEW CYS1678TYR MUTATION RESPONSIBLE OF LGMD2B IDENTIFIED IN A FAMILY FROM SOUTHERN ITALY
Abstract
A case of facioscapulohumeral muscular dystrophy and myasthenia gravis with positivity of anti-Ach receptor antibody: a fortuitous association?
Articolo
A new mutation detected by NGS in MT-ATP6 gene associated with MELAS and in silico 3D protein analysis
Abstract
A normative study of the Italian printed word version of the free and cued selective reminding test.
Articolo
Aceruloplasminemia: a multimodal imaging study in an Italian family with a novel mutation
Articolo
Acute bulbar palsy without ophtalmoplegia associated with anti-GD3 IgM antibodies.
Articolo
An unusual ALS onset with hyperhidrosis as frst clinical manifestation
Articolo
Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy
Articolo
Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy
Articolo
Arg143Ser is the most frequent variant in Limb Girdle Muscular Dystrophy-R9 in southern Italy
Abstract
Association of 5-HT6 receptor gene polymorphism C267T with Parkinson's disease
Abstract
CSF MALDI-TOF mass spectrometry protein profiling in Clinically Isolated Syndrome.
Articolo
Challenging functional connectivity data: machine learning application on essential tremor recognition
Articolo
Cognitive functioning in essential tremor without dementia: a clinical and imaging study
Articolo
Dropped head syndrome in a patient with FTD-ALS caused by abnormal expansion of C9orf72 gene.
Articolo
Early and rapidly progressing respiratory failure in a patient with amyotrophic lateral sclerosis: when FVC% is misleading
Articolo
Evaluation of rest tremor in different positions in Parkinson's disease and essential tremor plu
Articolo
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT
Abstract
Hypertension, seizures, and epilepsy: a review on pathophysiology and management
Articolo
Identification of differentially expressed genes in recessive axonal charcot marie tooth disease using PCR-SELECT cDNA substraction
Abstract
Impact of acute-phase complications and interventions on 6-month survival after stroke. A prospective observational study in four Italian Regions.
Abstract
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder?
Articolo
Migraine attack triggering a generalised seizure: is this a case of migralepsy or ictal epileptic headache?
Articolo
Neurofunctional correlates of attention rehabilitation in Parkinson's disease: an explorative study
Articolo
No evidence of association between Alpha 2 macroglobulin gene and Parkinson's disease in a case-control sample
Abstract
Opicapone-induced reversible myopathy in a patient with advanced Parkinson's disease and familial hyperCKemia
Articolo
Parkinson's Disease Sleep Scale 2: application in an Italian population.
Articolo
Prevalence of atrial fibrillation subtypes in the Italian elderly population. Progetto FAI. La Fibrillazione Atriale in Italia.
Abstract
Progressive supranuclear palsy with marked ventricular dilatation mimicking normal pressure hydrocephalus
Articolo
Reversible symmetrical external capsule hyperintensity as an early finding of autoimmune encephalitis
Articolo
Risk factors for unprovoked epileptic seizures in multiple sclerosis: a systematic review and meta-analysis.
Articolo
SMART: stroke-like migraine attacks after radiation therapy or seizures with migraine-like attacks after radiation therapy? Terms do matter in clinical practice.
Articolo
Septo-optic dysplasia plus bilateral perisylvian polymicrogyria: a case report.
Articolo
Serial MRI findings in brain anoxia leading to Lance-Adams syndrome: a case report.
Articolo
Targeted next-generation sequencing revealed a new mutation in GLRA1 gene in a family with Hereditary Hyperekplexia
Abstract
The contribution of surgical brain mapping to the understanding of the anatomo-functional basis of syntax: A critical review
Articolo
Validation of the Italian version of the Movement Disorder Society--Unified Parkinson's Disease Rating Scale.
Articolo
Vitamin E deficiency due to chylomicron retention disease im Marinesco-Sjogren syndrome
Abstract
Was the subject portrayed in "A Man" by Cornelis Anthonisz around 1530 really affected by progressive supranuclear palsy?
Articolo
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