Get started
Author

Gianfranco Puoti

Observed names: G Puoti, G. Puoti, PUOTI, Gianfranco, Puoti Gianfranco, Puoti, Gianfranco
Observed institutions: University of Parma, University of Campania "Luigi Vanvitelli", Luigi Sacco Hospital, Advanced Neural Dynamics (United States), Fondazione IRCCS Istituto Neurologico Carlo Besta, Case Western Reserve University, University of Milano-Bicocca, University of Naples Federico II
ORCID: 0000-0002-6452-2321
Observed ORCID: 0000-0002-6452-2321
OpenAlex ID: A5036073639
Sporadic human prion diseases: molecular insights and diagnosis
2012 · Gianfranco Puoti, Alberto Bizzi, et al. · The Lancet Neurology · 365
Variably protease‐sensitive prionopathy: A new sporadic disease of the prion protein
2010 · Wen‐Quan Zou, Gianfranco Puoti, et al. · Annals of Neurology · 277
Sporadic Creutzfeldt-Jakob disease: Co-occurrence of different types of PrP Sc in the same brain
1999 · G. Puoti, G. Giaccone, et al. · Neurology · 196
A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob disease
2012 · Clive Hamlin, Gianfranco Puoti, et al. · Neurology · 149
PDF
Human prion diseases: surgical lessons learned from iatrogenic prion transmission
2016 · David J. Bonda, Sunil Manjila, et al. · Neurosurgical FOCUS · 134
PDF
Hereditary Cerebral Hemorrhage With Amyloidosis Associated With the E693K Mutation of APP
2010 · Orso Bugiani, Giorgio Giaccone, et al. · Archives of Neurology · 117
PDF
Amyloid-β42 Interacts Mainly with Insoluble Prion Protein in the Alzheimer Brain
2011 · Wen-Quan Zou, Xiangzhu Xiao, et al. · Journal of Biological Chemistry · 80
Variably Protease-Sensitive Prionopathy: a Novel Disease of the Prion Protein
2011 · Pierluigi Gambetti, Gianfranco Puoti, et al. · Journal of Molecular Neuroscience · 71
Creutzfeldt–Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene
2000 · G. Rossi, G. Giaccone, et al. · Neurology · 64
Creutzfeldt‐Jakob Disease: Carnoy's Fixative Improves the Immunohistochemistry of the Proteinase K‐ Resistant Prion Protein
2000 · Giorgio Giaccone, Barbara Canciani, et al. · Brain Pathology · 55
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics
2020 · Ignazio Cali, Gianfranco Puoti, et al. · Scientific Reports · 46
PDF
Sporadic Creutzfeldt-Jakob Disease: The Extent of Microglia Activation Is Dependent on the Biochemical Type of PrPSc
2005 · Gianfranco Puoti, Giorgio Giaccone, et al. · Journal of Neuropathology & Experimental Neurology · 38
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease
2020 · Satish K. Nemani, Xiangzhu Xiao, et al. · Acta Neuropathologica Communications · 34
PDF
Polymorphism at codon 129 ofPRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation
2000 · Gianfranco Puoti, Giacomina Rossi, et al. · Annals of Neurology · 28
MRI "fogging" in cerebellar ischaemia: case report
1997 · A. Scuotto, S. Cappabianca, et al. · Neuroradiology · 26
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene
2003 · V. Pietrini, G. Puoti, et al. · Neurology · 23
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son
2003 · G Puoti · Journal of Medical Genetics · 23
PDF
12-months prospective Pentraxin-3 and metabolomic evaluation in multiple sclerosis patients treated with glatiramer acetate
2020 · E. Signoriello, P. Iardino, et al. · Journal of Neuroimmunology · 21
Coexistence of Cavernous Hemangioma and Other Vascular Malformations of the Orbit
2014 · Diego Strianese, Manuela Napoli, et al. · The Neuroradiology Journal · 21
A New Prion Disease: Protease‐Sensitive Prionopathy
2011 · Pierluigi Gambetti, Gianfranco Puoti, et al. · 19
Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease.
2016 · Paola Imbriani, Girolama Alessandra Marfia, et al. · PubMed · 17
Non-alcoholic acute Wernicke's encephalopathy: Role of MRI in non typical cases
2012 · Andrea Elefante, Gianfranco Puoti, et al. · European Journal of Radiology · 17
Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques
2004 · Gianfranco Puoti, Lucia Limido, et al. · Neurology · 17
Protease-sensitive prions with 144-bp insertion mutations
2013 · Xiangzhu Xiao, Ignazio Cali, et al. · Aging · 16
The ε Isoform of 14-3-3 Protein Is a Component of the Prion Protein Amyloid Deposits of Gerstmann-Sträussler-Scheinker Disease
2007 · Giuseppe Di Fede, Giorgio Giaccone, et al. · Journal of Neuropathology & Experimental Neurology · 16
Works count: 132
Citation count: 2,089
H-index: 19
I10-index: 32
Year
Topic
Type