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Affiliazione : Università degli Studi della Campania Luigi Vanvitelli
Profilo Ricercatore
Gianfranco Puoti
Neurologo
Is the pathology of posterior cortical atrophy clinically predictable?
Systematic Review on the Role of Lobar Cerebral Microbleeds in Cognition
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
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances"
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
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic Stroke
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
Rehabilitation of gesture imitation: a case study with fMRI
Migraine as possible red flag of PFO presence in suspected demyelinating disease
MRI 'fogging' in cerebellar ischaemia: Case report
12-months prospective Pentraxin-3 and metabolomic evaluation in multiple sclerosis patients treated with glatiramer acetate
Characterization of prion disease associated with a two-octapeptide repeat insertion
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease
A novel missense mutation in CAV3 gene in an Italian family with persistent hyperCKemia, myalgia and hypercholesterolemia: Double-trouble
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics
Corrigendum to “A novel missense mutation in CAV3 gene in an Italian family with persistent hyperCKemia, myalgia and hypercholesterolemia: Double-trouble” [Clin. Neurol. Neurosurg. 191 (2020) 105687](S0303846720300305)(10.1016/j.clineuro.2020.105687)
Expanding the spectrum of SPTLC1-related disorders beyond hereditary sensory and autonomic neuropathies: A novel case of the distinct “S331 syndrome”
Minimally invasive percutaneous treatment for osteoid osteoma of the Spine. A case report
Predictive factors of volumetric reduction in lumbar disc herniation treated by O2-o3 chemiodiscolysis
Progressive multifocal leukoencephalopathy presenting with bilateral myoclonus: a case report
A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient
Dramatic neurological debut in a case of Köhlmeier-Degos disease
Unusual CLIPPERS presentation and role of MRI examination in the proper diagnostic assessment: A case report
Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease
Human prion diseases: Surgical lessons learned from iatrogenic prion transmission
Synthetic Aβ peptides acquire prion-like properties in the brain
Variably protease-sensitive prionopathy in an apparent cognitively normal 93-year-old
A mutation in the 5′-UTR of GRN gene associated with frontotemporal lobar degeneration: Phenotypic variability and possible pathogenetic mechanisms
Coexistence of cavernous hemangioma and other vascular malformations of the orbit: A report of three cases
New-onset refractory status epilepticus mimicking herpes virus encephalitis
Protease-sensitive prions with 144-bp insertion mutations
A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob disease
Sporadic human prion diseases: Molecular insights and diagnosis
Amyloid-β42 interacts mainly with insoluble prion protein in the Alzheimer brain
Variably protease-sensitive prionopathy: A novel disease of the prion protein
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP
Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein
A novel insertional mutation in the prion protein gene: Clinical and bio-molecular findings
The ε isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease
Sporadic Creutzfeldt-Jakob disease: The extent of microglia activation is dependent on the biochemical type of PrPSc
Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques [5] (multiple letters)
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene
Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion protein
Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation [3]
Sporadic Creutzfeldt-Jakob disease: Co-occurrence of different types of PrP(Sc) in the same brain
