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PUOTI, Gianfranco

PUOTI, Gianfranco  

Dipartimento di Scienze Mediche e Chirurgiche Avanzate (DAMSS)  

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Risultati 1 - 20 di 99 (tempo di esecuzione: 0.059 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.
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
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
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
A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms 1-gen-2014 Puoti, Gianfranco; Lerza, Mc; Ferretti, Mg; Bugiani, O; Tagliavini, F; Rossi, G.
A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. 1-gen-2008 Mauro, C.; Giaccone, G.; Piscosquito, G.; Lavorgna, A.; Nigro, M.; DI FEDE, G.; Leonardi, A.; Formisano, S.; Tagliavini, F.; Cotrufo, R.; Coppola, Cinzia; Puoti, Gianfranco
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease 1-gen-2020 Nemani, Satish K; Xiao, Xiangzhu; Cali, Ignazio; Cracco, Laura; Puoti, Gianfranco; Nigro, Massimiliano; Lavrich, Jody; Bharara Singh, Anuradha; Appleby, Brian S; Sim, Valerie L; Notari, Silvio; Surewicz, Witold K; Gambetti, Pierluigi
A Novel Missense Mutation in CAV3 Gene in an Italian Family With Persistent hyperCKemia, Myalgia and Hypercholesterolemia: Double-trouble 1-gen-2020 Bruno, Giorgia; Puoti, Gianfranco; Oliva, Mariano; Colavito, Davide; Allegorico, Lia; Napolitano, Filomena; Sampaolo, Simone
A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient. 1-gen-2019 Oliva, M; Capaldo, G; D'Amico, A; Colavito, D; Elefante, A; Straccia, G; Ugga, L; Puoti, G
A peculiar report of rare multifocal "ganglio-glioneurocytoma" 1-gen-2017 Schettino, C; Capaldo, G; Giangaspero, F; Dato, C; Puoti, G; Pappatà, S; D'Amico, A; Di Iorio, G; Melone, M
Alemtuzumab-Related Lymphocyte Subset Dynamics and Disease Activity or Autoimmune Adverse Events: Real-World Evidence 1-gen-2023 Signoriello, Elisabetta; Lus, Giacomo; Saccà, Francesco; Puthenparampil, Marco; Coppola, Cinzia; Di Pietro, Andrea; Puoti, Gianfranco; Criscuolo, Maria Cristina; Foschi, Matteo; Miele, Giuseppina; Abbadessa, Gianmarco; Brescia Morra, Vincenzo; Gallo, Paolo; Bonavita, Simona; Sormani, Maria Pia; Signori, Alessio
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
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.; 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.
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.