PUOTI, Gianfranco

PUOTI, Gianfranco  

Dipartimento di Scienze Mediche e Chirurgiche Avanzate (DAMSS)  

Risultati 1 - 20 di 96 (tempo di esecuzione: 0.022 secondi).
Titolo Data di pubblicazione Autore(i) File
12-months prospective Pentraxin-3 and metabolomic evaluation in multiple sclerosis patients treated with glatiramer acetate 1-gen-2020 Signoriello, E.; Iardino, P.; Casertano, S.; De Lucia, D.; Pucciarelli, A.; Puoti, G.; Chiosi, E.; Lus, G.
Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain 1-gen-2011 Zou, Wq; Xiao, X; Yuan, J; Puoti, Gianfranco; Fujioka, H; Wang, X; Richardson, S; Zhou, X; Zou, R; Li, S; Zhu, X; Mcgeer, Pl; Mcgeehan, J; Kneale, G; RINCON LIMAS, De; FERNANDEZ FUNEZ, P; Lee, Hg; Smith, Ma; Petersen, Rb; Guo, Jp
Analyses of the Protein Tau to Help Determine Whether the Newly Discovered Protease-Sensitive Prionopathy is the Sporadic Form of Gerstmann-Sträussler-Scheinker Disease (GSS) 1-gen-2010 Puoti, Gianfranco
Atypical Progressive Multifocal Leukoencephalopathy in a Kidney Transplant Recipient With Improving Symptoms After Immunocompetence Recovery 1-gen-2020 Bruno, Giorgia; Miele, Giuseppina; Abbadessa, Gianmarco; Di Pietro, Andrea; Russo, Camilla; Negro, Alberto; Bonavita, Simona; Puoti, Gianfranco
“Borderline” idiopathic CD4+ T-cell lymphocytopenia presenting with atypical progressive multifocal leukoencephalopathy 1-gen-2020 Dato, C.; Elefante, A.; Coppola, C.; Melone, M. A. B.; Lus, G.; Costagliola, A.; Bruno, G.; Puoti, G.
A case of Kohlmeier-Degos disease with dramatic neurological involvment 1-gen-2017 Saracino, D; D'Armiento, Fp; Napolitano, M; Ayala, F; Di Iorio, G; Puoti, G
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 1-gen-2020 Cali, Ignazio; Cracco, Laura; Saracino, Dario; Occhipinti, Rossana; Coppola, Cinzia; Appleby Brian, Stephen; Puoti, Gianfranco
Characterization of prion disease associated with a two-octapeptide repeat insertion 1-gen-2021 Brennecke, N.; Cali, I.; Mok, T. H.; Speedy, H.; Consortium, G. E. R.; Hosszu, L. L. P.; Stehmann, C.; Cracco, L.; Puoti, G.; Prior, T. W.; Cohen, M. L.; Collins, S. J.; Mead, S.; Appleby, B. S.
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic Stroke 1-gen-2021 Bruno, G.; Ritelli, M.; Di Pietro, A.; Cipriano, L.; Colombi, M.; Lus, G.; Puoti, G.
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 1-gen-2016 Saracino, D; Coppola, C; Puoti, G; Lus, G; Dato, C; le Ber, I; Caroppo, P; Piccoli, F; Tagliavini, F; Di Iorio, G; Rossi, G
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 1-gen-2017 Coppola, Cinzia; Saracino, Dario; Puoti, Gianfranco; Lus, Giacomo; Dato, Clemente; Le Ber, Isabelle; Pariente, Jeremie; Caroppo, Paola; Piccoli, Elena; Tagliavini, Fabrizio; DI IORIO, Giuseppe; Rossi, Giacomina
Co-existence of PrP D Types 1 and 2 in Sporadic Creutzfeldt-Jakob Disease of the VV Subgroup: Phenotypic and Prion Protein Characteristics 1-gen-2020 Cali, Ignazio; Puoti, Gianfranco; Smucny, Jason; Michael Curtiss, Paul; Cracco, Laura; Kitamoto, Tetsuyuki; Occhipinti, Rossana; Lloyd Cohen, Mark; Stephen Appleby, Brian; Gambetti, Pierluigi
Coexistence of cavernous hemangioma and other vascular malformations of the orbit. A report of three cases 1-gen-2014 Strianese, D; Napoli, M; Russo, C; D'Errico, A; Scotti, N; Puoti, Gianfranco; Bonavolontà, G; Tranfa, F; Briganti, F.
A comparison of Tau and 14-3-3 protein in the diagnosis of Creitzfeldt-Jakob disease 1-gen-2012 Hamlin, C; Puoti, Gianfranco; Berri, S; Sting, E; Harris, C; Cohen, M; Spear, C; Bizzi, A; Debanne, Sm; Rowland, Dy
CORRELATI CLINICO-STRUMENTALI IN UN CASO DI CREUTZFELD- JACOB A LUNGA SOPRAVVIVENZA. 1-gen-2000 Puoti, Gianfranco; O., Bugiani; Lus, Giacomo; F., Romano; Scuotto, Assunta; F., Tagliavini; R., Cotrufo 
Creutzfeldt-Jakob Disease 1-gen-2011 Gambetti, P; Puoti, G; Cali, I; Kong, Q; Zou, W
Creutzfeldt-Jakob disease (CJD) associated with V210I PRNP mutation: phenotypic and molecular genetic analysis 1-gen-2003 Puoti, Gianfranco; DI FEDE, G; Mangieri, M; Limido, L; Giaccone, G; Rossi, G; Cotrufo, R; Bugiani, O; Tagliavini, F.
Creutzfeldt-Jakob disease (CJD) in italian patients with PRNP V210I mutation: an epidemiological and clinical evaluation 1-gen-2008 Mellina, V; Ladogana, A; Poleggi, A; Puopolo, M; Almonti, S; Capellari, S; Puoti, Gianfranco; Giaccone, G; DI FEDE, G; Coppola, Cinzia; Cotrufo, R; Tagliavini, F; Parchi, P; Pocchiari, M.
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene 1-gen-2003 Pietrini, V; Puoti, Gianfranco; Limido, L; Rossi, G; DI FEDE, G; Giaccone, G; Mangieri, M; Tedeschi, F; Bondavalli, A; Mancia, D; Bugiani, O; Tagliavini, F.
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene 1-gen-2000 Rossi, G; Giaccone, G; Giampaolo, L; Iussich, S; Puoti, Gianfranco; Frigo, M; Cavaletti, G; Frattola, L; Bugiani, O; Tagliavini, F.