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Affiliazione : Università degli Studi della Campania Luigi Vanvitelli
Profilo Ricercatore
Cinzia Coppola
Neurologa
Is the pathology of posterior cortical atrophy clinically predictable?
Immunomodulatory effects of ocrelizumab and candidate biomarkers for monitoring treatment response in multiple sclerosis
Systematic Review on the Role of Lobar Cerebral Microbleeds in Cognition
Understanding and managing the impact of the Covid-19 pandemic and lockdown on patients with multiple sclerosis
Apparently isolated CNS involvement in Erdheim-Chester disease: Case report
Exploring Circulating Long Non-Coding RNAs in Mild Cognitive Impairment Patients' Blood
Plasma Small Extracellular Vesicles with Complement Alterations in GRN/ C9orf72 and Sporadic Frontotemporal Lobar Degeneration
Alemtuzumab-Related Lymphocyte Subset Dynamics and Disease Activity or Autoimmune Adverse Events: Real-World Evidence
Plasma Small Extracellular Vesicle Cathepsin D Dysregulation in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration
Predictors of Cladribine Effectiveness and Safety in Multiple Sclerosis: A Real-World, Multicenter, 2-Year Follow-Up Study
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances"
MicroRNA Expression Signature in Mild Cognitive Impairment Due to Alzheimer's Disease
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman Empire
"Borderline" idiopathic CD4+ T-cell lymphocytopenia presenting with atypical progressive multifocal leukoencephalopathy
Role of Ocrelizumab in modulating gene and microRNA expression in multiple sclerosis
Diagnostic contribution of magnetic resonance imaging in an atypical presentation of motor neuron disease
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion
Non-alcoholic acute Wernicke's encephalopathy: role of MRI in non typical cases
Verapamil Inhibits Ser202/Thr205 Phosphorylation of Tau by Blocking TXNIP/ROS/p38 MAPK Pathway.
A novel insertional mutation in the prion protein gene: Clinical and bio-molecular findings
“Brain Wellness in Comiziano”: Epidemiological Study on Potential Protective Factors for Alzheimer’s Disease in a Small Italian Village
Exploring Circulating Long Non-Coding RNAs in Mild Cognitive Impairment Patients’ Blood
Semantic and right temporal variant of FTD: Next generation sequencing genetic analysis on a single-center cohort
Primary Progressive Aphasia Associated With GRN Mutations
A novel DNM2 mutation in a case with a pure sensory axonal polyneuropathy
One novel GRN null mutation, two different aphasia phenotypes
Delayed post-hypoxic leukoencephalopathy with a peculiar autoantibody association
Preliminary data from a study on clinical and neuroradiological correlations between cerebral microbleeds and different subtypes of mild cognitive impairment
Novel VCP mutations expand the mutational spectrum of frontotemporal dementia
A case of progressive frontal lobe syndrome in a sporadic form of Cerebral Amyloid Angiopathy: A singular overlap with fronto-temporal dementia?
miR-338-3p is over-expressed in blood, CFS, serum and spinal cord from sporadic amyotrophic lateral sclerosis patients.
A novel de novo insertional mutation in the prion protein gene characterized by slowly progressive atypical dementia: Neuropathological and biochemical findings
A miRNA signature in leukocytes from sporadic amyotrophic lateral sclerosis.
A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration
Intra-arterial or intravenous thrombolysis for acute ischemic stroke? The SYNTHESIS pilot trial.
