Skip to Main Content (Press Enter)

Logo UNIPV
  • ×
  • Home
  • Corsi
  • Insegnamenti
  • Professioni
  • Persone
  • Pubblicazioni
  • Strutture

UNIFIND
Logo UNIPV

|

UNIFIND

unipv.it
  • ×
  • Home
  • Corsi
  • Insegnamenti
  • Professioni
  • Persone
  • Pubblicazioni
  • Strutture
  1. Pubblicazioni

NEUROLOGY

Rivista
Codice:
E117266
ISSN:
0028-3878
  • Dati Generali

Dati Generali

Pubblicazioni (153)

  • ascendente
  • decrescente
"Gluing" phenotypes together The case of GLUT1
Articolo
A double-blind, placebo-controlled, multiple migraine attack study.
Articolo
A field potential analysis on the effects of lamotrigine, GP 47779, and felbamate in neocortical slices
Articolo
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
Articolo
A propensity score analysis for comparison of T-3b and VATET in myasthenia gravis
Articolo
A prospective cohort study in JCV and non JCV-related leukoencephalopathies in HIV patients
Abstract
ALS on Italian professional soccer players: the epidemic is still ongoing and soccer-specific
Abstract
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
Articolo
Acute Disseminated Encephalomyelitis (ADEM): A Prospective Study on 122 Adults
Abstract
Acute late-onset encephalopathy after radiotherapy: an unusual life-threatening complication
Articolo
Acute tolerance to the tremorolytic effect of primidone.
Articolo
Acute vs chronic effects of l-dopa on bladder function in patients with mild Parkinson disease
Articolo
Age and sex prevalence estimate of Joubert syndrome in Italy
Articolo
Alcohol intake and the risk of intracerebral hemorrhage in the elderly: The MUCH-Italy
Articolo
Amyotrophic lateral sclerosis: oxidative energy metabolism and calcium homeostasis in peripheral blood lymphocytes
Articolo
Antiepileptic drugs and intrauterine death: A prospective observational study from EURAP
Articolo
Antithrombotic medications and the etiology of intracerebral hemorrhage: The MUCH-Italy
Articolo
Association Between Semiology and Anatomo-functional Localization in Patients With Cingulate Epilepsy: A Cohort Study
Articolo
Association of Slowly Expanding Lesions on MRI With Disability in People With Secondary Progressive Multiple Sclerosis
Articolo
Author response: Increased resting cerebral blood flow in adult Fabry disease: MRI arterial spin labeling study
Articolo
Brain damage as detected by cDNA-microarray in the spinal fluid of patients with Aicardi-Goutieres syndrome.
Articolo
Cerebellar signs in celiac disease.
Articolo
Cervical cord lesion load is associated with disability independently from atrophy in MS
Articolo
Choreiform syndrome associated with fluoxetine treatment in a patient with deficient CYP2D6 activity.
Articolo
Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency
Articolo
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum
Articolo
Clinical and subclinical dopaminergic dysfunction in autosomal recessive PARK6-linked parkinsonism: An F-18-dopa PET study
Abstract
Clinical characterization of Italian families affected by purely focal idiopathic torsion dystonia
Abstract
Clustering of ALS patients in central Italy due to the occurrence of the L84F SOD1 gene mutation
Articolo
Cognitive and psychosocial features of childhood and juvenile MS
Articolo
Common Genetic Markers and Prediction of Recurrent Events after Ischemic Stroke in Young Adults
Articolo
Comorbidity and medication in REM sleep behavior disorder: A multicenter case-control study
Articolo
Comparison of levetiracetam and controlled-release carbamazepine in newly diagnosed epilepsy.
Articolo
Complete stable remission and autoantibody specificity in myasthenia gravis
Articolo
Congenital muscular dystrophies with cognitive impairment: A population study
Articolo
Congenital muscular dystrophies with defective glycosylation of dystroglycan: A population study
Articolo
Correlation of clinical and molecular features in spinal bulbar muscular atrophy
Articolo
Cuban optic neuropathy
Articolo
Cytosol protein kinase C downregulation in fibroblasts from Alzheimer's disease patients.
Articolo
Detection of HTLV-III specific IgG in the CSF from patient with AIDS and encephalitis.
Articolo
Diagnosis of glycogenosis type II
Articolo
Differences in Age-related Retinal and Cortical Atrophy Rates in Multiple Sclerosis
Articolo
Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
Articolo
Does screening for adverse effects improve health outcomes in epilepsy? A randomized trial
Articolo
Dose-dependent teratogenicity of valproate in mono- and polytherapy: An observational study.
Articolo
Dynamic Properties of Saccades Identify Forms of Spinocerebellar Ataxia
Abstract
EARLY-ONSET HEAD TITUBATION IN A CHILD WITH PORETTI-BOLTSHAUSER SYNDROME
Articolo
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes
Articolo
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.
Articolo
Effects of delayed-release dimethyl fumarate on MRI measures in the phase 3 CONFIRM study
Articolo
Efficacy of propafenone in paramyotonia congenita
Articolo
Electrophysiologic patterns of oral-pharyngeal swallowing in parkinsoniansyndromes.
Articolo
Eletriptan vs sumatriptan: a double-blind, placebo-controlled, multiple migraine attack study
Articolo
Environmental risk factors for REM sleep behavior disorder: A multicenter case-control study
Articolo
Enzyme replacement therapy (ERT) in adult-onset type II glycogenosis (GSDII)
Contributo in Atti di convegno
Epileptic skew deviation.
Articolo
Evidence of thalamic gray matter loss in pediatric multiple sclerosis
Articolo
Evidence-based guideline: Antiepileptic drug selection for people with HIV/AIDS: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Ad Hoc Task Force of the Commission on Therapeutic Strategies of the International League Against Epilepsy.Quality Standards Subcommittee of the American Academy of Neurology; Ad Hoc Task Force of the Commission on Therapeutic Strategies of the International League Against Epilepsy.
Articolo
Facial nerve is liable to pressure palsy.
Articolo
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene.
Articolo
Family history of idiopathic REM behavior disorder a multicenter case-control study
Articolo
Fibroblasts of patients affected by Down's syndrome oversecrete amyloid precursor protein and are hyporesponsive to protein kinase C stimulation.
Articolo
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome.
Articolo
Finding a common path to the assessment of persons with intellectual development disorders
Articolo
GCSF-mobilized hematopoietic stem cells in CMS ischemic lesion
Abstract
Genetic testing to prevent adverse reactions to antiepileptic drugs: Primum non nocere
Articolo
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence from the COURAGE-PD Consortium
Articolo
Global investigation and meta-analysis of the C9orf72 (G(4)C(2))(n) repeat in Parkinson disease
Articolo
Hallucinations and sleep-wake cycle in PD: A 24-hour continuous polysomnographic study
Articolo
Hand weakness from a precentral gyrus infarct with intermittent hypotension.
Articolo
Hemianesthesia, sensory neglect, and defective access to conscious experience
Articolo
Hemorrhagic transformation of brain infarct: predictability in the first 5 hours from stroke onset and influence on clinical outcome.
Articolo
High prevalence and geographical variation of mysthenia gravis in an Italian area
Contributo in Atti di convegno
Hypnic headache: PSG evidence of both REM- and NREM-related attacks
Articolo
Impulsive-compulsive behaviors in parkin-associated Parkinson disease
Articolo
Incidence and Long-term Functional Outcome of Neurologic Disorders in Hospitalized Patients With COVID-19 Infected With Pre-Omicron Variants
Articolo
Increased resting cerebral blood flow in adult Fabry disease: MRI arterial spin labeling study
Articolo
Infantile ascending hereditary spastic paralysis (IAHSP) - Clinical features in 11 families
Articolo
Internal borderzone infarction following acute middle cerebral artery occlusion.
Articolo
Intracranial Nonstenosing Atherosclerotic Plaques Assessed With Vessel Wall MRI in Patients With Embolic Stroke of Undetermined Source
Articolo
Investigating the SGCE gene in myoclonic syndromes: Guidelines for diagnostic testing
Abstract
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy
Articolo
Largely increased risk of amyotrophic lateral sclerosis among Italian professional soccer players
Abstract
Left caloric vestibular stimulation ameliorates right hemianesthesia
Articolo
Limbic hyperconnectivity in the vegetative state.
Articolo
Long-term 1-acetylcarnitine treatment in Alzheimer's disease
Articolo
Lower motor neuron disease with respiratory failure caused by a novel MAPT mutation.
Articolo
MRI and brainstem auditory evoked potential evidence of eighth cranial nerve involvement in multiple sclerosis.
Articolo
MRI in multiple sclerosis during the menstrual cycle: relationship with sex hormone patterns.
Articolo
Management and treatment of glycogenosis type II
Articolo
Migraine with aura and white matter abnormalities: Notch3 mutation.
Articolo
Migraine with aura and white matter abnormalities:Notch3 mutation.
Articolo
Motor network efficiency and disability in multiple sclerosis
Articolo
Multiple Sclerosis and Occupational Exposures: A Case-Control Study
Abstract
Neuro-Ophthalmological Findings in Two Italian Adult Siblings with Ataxia-Telangiectasia-Like Disorder (P06.017)
Abstract
Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndrome
Articolo
New screening test for muscle glycogenosis
Abstract
Noninvasive vagus nerve stimulation as acute therapy for migraine: The randomized PRESTO study
Articolo
Nonverbal Cognitive Skills in Children With Aicardi Goutières Syndrome
Articolo
Novel CLN3 mutation causing autophagic vacuolar myopathy.
Articolo
Outcome after Two Years of Enzyme Replacement Therapy (ERT) in 29 Patients with Late-Onset Type II Glycogenosis (GSDII)
Contributo in Atti di convegno
PRRT2 gene mutations From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine
Articolo
Pearls & Oy-sters: Marionette Walk in Parkinson Disease
Articolo
Peripheral proteasome and caspase activity in Parkinson disease and Alzheimer disease
Articolo
Periventericular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion.
Articolo
Periventricular heterotopia in fragile X syndrome.
Articolo
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion.
Articolo
Pisa syndrome in Parkinson disease: An observational multicenter Italian study
Articolo
Post infectious inflammatory disorders: subgroup based on prospective follow-up
Articolo
Post-infectious inflammatory disordes:sub-groups based on prospective follow-up.
Articolo
Posterior brain damage and cognitive impairment in pediatric multiple sclerosis
Articolo
Postinfectious neurologic syndromes: A prospective cohort study
Articolo
Postprandial and orthostatic hypotension in Parkinson's disease.
Articolo
Presyrinx in children with Chiari malformations
Articolo
Primary Lateral Sclerosis Presenting with Focal Onset Spreading Through Contiguous Neuroanatomic Regions
Articolo
Ptosis as a feature of late-onset glycogenosis type II.
Articolo
Quality of care and cost-effectiveness of ALS interdisciplinary centers: The Quac study
Abstract
REM behavior disorder associated with epileptic seizures
Articolo
Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy
Articolo
Rapid progression of familial amyloidotic polyneuropathy: a multinational natural history study
Articolo
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus
Articolo
Recombinant alglucosidase alpha (rhGAA) in adult-onset type II glycogenosis (GSDII): A follow-up study before and after treatment
Contributo in Atti di convegno
Recurrent myelitis in patients with hepatitis C virus infection
Abstract
Renal tubular impairment during riluzole therapy
Articolo
Renal tubular impairment during riluzole therapy.
Articolo
Reply from the authors
Articolo
Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment
Articolo
Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment - Reply
Articolo
Scrapie infectivity and prion protein are distributed in the same pH range in agarose isoelectric focusing.
Articolo
Seizure control and treatment in pregnancy. Observations from the EURAP Epilepsy Pregnancy Registry
Articolo
Serial study of gadolinium-DTPA MRI enhancement in multiple sclerosis.
Articolo
Severe recurrent myelitis in patients with hepatitis C virus infection
Articolo
Severe recurrent myelitis in patients with hepatitis C virus infection patients
Articolo
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
Articolo
Spectrum of mutations in the gene for epsilon-sarcoglycan (SGCE) in myoclonus-dystonia syndrome (MDS, DYT11)
Abstract
Status epilepticus migrainosus: Clinical, electrophysiologic, and imaging characteristics
Articolo
Structure of the human mitochondrial monoamine oxidase B: New chemical implications for neuroprotectant drug design
Articolo
Sympathetic and parasympathetic baroreflex dysfunction in familial dysautonomia
Articolo
Tactile and proprioceptive dysfunction differentiates cervical dystonia with and without tremor
Articolo
Targeted next-generation sequencing panels in the diagnosis of Charcot-Marie-Tooth disease
Articolo
Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy.
Articolo
The PINK1 phenotype can be indistinguishable from idiopathic Parkinson disease
Articolo
The diverse phenotype and genotype of pantothenate kinase-associated neurodegeneration
Articolo
The epsilon-sarcoglycan gene in myoclonic syndromes
Articolo
The natural history of Aicardi-Goutières syndrome: follow-up of 11 Italian patients
Articolo
The phenotype of SCN8A developmental and epileptic encephalopathy
Articolo
Transcranial Doppler in acute hemispheric brain infarction.
Articolo
Truncating Variants in RFC1 in Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome
Articolo
Update on blepharospasm - Report from the BEBRF International Workshop
Articolo
Use of Bacille Calmette-Guèrin (BCG) in multiple sclerosis.
Articolo
Varicella zoster virus-associated polyradiculoneuritis
Articolo
Visual cortex hyperexcitability in migraine in response to sound-induced flash illusions
Articolo
White and gray matter damage in primary progressive MS: The chicken or the egg?
Articolo
No Results Found
  • «
  • ‹
  • {pageNumber}
  • ›
  • »
{startItem} - {endItem} di {itemsNumber}
  • Utilizzo dei cookie

Realizzato con VIVO | Designed by Cineca | 25.12.3.0