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CALI', IGNAZIO

CALI', IGNAZIO  

Dipartimento di Medicina e Chirurgia  

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Titolo Data di pubblicazione Autore(i) File
A novel de novo insertional mutation in the PrP gene characterized by slowly progressive atypical dementia: Neuropathological and biochemical findings 1-gen-2014 Puoti, G; Saracino, D; Coppola, C; Cali, I
A Novel Mechanism of Phenotypic Heterogeneity in Creutzfeldt-Jakob Disease 1-gen-2020 Satish, K Nemani; Xiao, Xiangzhu; Cali, I; Cracco, Laura; Puoti, Gianfranco; Nigro, Massimiliano; Lavrich, Jody; Anuradha Bharara Singh, ; Brian, S Appleby; Valerie, L Sim; Notari, Silvio; Witold, K Surewicz; Gambetti, Pierluigi
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques 1-gen-2023 Bayazid, R; Orru', C; Aslam, R; Cohen, Y; Silva-Rohwer, A; S-K, Lee; Occhipinti, R; Kong, Q; Shetty, S; Cohen M, L Cohen; Caughey, B; L B, Schonberger; B S, Appleby; Cali, I
Amyloid fibrils from the N-terminal prion protein fragment are infectious 1-gen-2016 Choi, Jk; Cali, I; Surewicz, K; Kong, Q; Gambetti, P; Surewicz, Wk.
Amyloid-β pathology in iatrogenic Creutzfeldt-Jakob disease: a multi-center study 1-gen-2016 Cali, I; M L, Cohen; Kofskey, D; Couce, M; G H, Jansen; Collins, S; Haїk, S; J P, Brandel; S C, Duyckaerts; E D, Belay; R A, Maddox; J G, Safar; Gambetti, P; Schonberger L, B.
Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report 1-gen-2022 Carrasco, Ae; Appleby, Bs; Cali, I; Okhravi, Hr.
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 1-gen-2020 Cali, I; Cracco, L; Saracino, D; Occhipinti, R; Coppola, C; Appleby BS and Puoti, G
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion 1-gen-2021 Brennecke, N; Cali, I; Mok, Th; Speedy, H; Genomics England Research Consortium, ; Llp, Hosszu; Stehmann, C; Cracco, L; Puoti, G; Prior, Tw; Cohen, Ml; Collins, Sj; Mead, S; Appleby, Bs.
Classification of sporadic Creutzfeldt-Jakob disease revisited 1-gen-2006 Cali, I; Castellani, R; Yuan, J; Al-Shekhlee, A; Cohen, Ml; Xiao, X; Moleres, Fj; Parchi, P; Zou, Wq; Gambetti, P
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics 1-gen-2020 Cali, I; Puoti, G; Smucny, J; Curtiss, Pm; Cracco, L; Kitamoto, T; Occhipinti, R; Cohen, Ml; Appleby, Bs; Gambetti, P
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics 1-gen-2009 Cali, I; Castellani, R; Alshekhlee, A; Cohen, Y; Blevins, J; Yuan, J; Langeveld, Jp; Parchi, P; Safar, Jg; Zou, Wq; Gambetti, P
Co-occurrence of chronic traumatic encephalopathy and prion disease 1-gen-2018 Nemani, Sk; Notari, S; Cali, I; Alvarez, Ve; Kofskey, D; Cohen, M; Stern, Ra; Appleby, B; Abrams, J; Schonberger, L; Mckee, A; Gambetti, P.
Co-occurrence of Distinct Types of Scrapie Prion Protein in Sporadic Creutzfeldt-Jakob Disease 1-gen-2013 Cali, I; Puoti, G; Cracco, L; Iyer, S; J P, Langeveld; Kitamoto, T; Notari, S; W Q, Zou; Gambetti, P
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype 1-gen-2009 Ghoshal, N; Cali, I; Perrin, Rj; Josephson, Sa; Sun, N; Gambetti, P; Morris, Jc
Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease 1-gen-2014 Xiao, X; Yuan, J; Qing, L; Cali, I; Mikol, J; Delisle, Mb; Uro-Coste, E; Zeng, L; Abouelsaad, M; Gazgalis, D; Martinez, Mc; Wang, Gx; Brown, P; Ironside, Jw; Gambetti, P; Kong, Q; Zou, Wq.
Distinct disease phenotypes and PrP type 1 variants in Creutzfeldt-Jakob disease with codon 129MM genotype 1-gen-2021 Bayazid, R; Aslam, R; Cohen, Y; L B, Schonberger; M L, Cohen; B S, Appleby; Cali, I
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone 1-gen-2015 Cali, I; Miller, Cj; Parisi, Je; Geschwind, Md; Gambetti, P; Schonberger, Lb
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. 1-gen-2015 Cali, I; Miller, C; Kitamoto, T; Parisi, J; Geschwind, M; Gambetti, P; Schonberger L, B.
Distinct strain of Amyloid beta and pathogenic tau protein in iatrogenic Creutzfeldt-Jakob disease. 1-gen-2019 J G, Safar; Kim, C; Haldiman, T; Ashok, A; Cali, I; M L, Cohen; Haїk, S; Parchi, P; Giaccone, G; S J, Collins; Kofskey, D; Wang, H; C A, Mclean; J P, Brandel; Privat, N; Sazdovitch, V; Duyckaerts, C; Kitamoto, T; E D, Belay; R A, Maddox; Tagliavini, F; Pocchiari, M; B S, Appleby; Gambetti, P; Gelpi, E; A C, Mckee; Ironside, J; and Schonberger L, B.
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host 1-gen-2024 Cracco, Laura; Cali', Ignazio; Cohen, Mark L.; Aslam, Rabail; Notari, Silvio; Kong, Qingzhong; Newell, Kathy L.; Ghetti, Bernardino; Appleby, Brian S.; Gambetti, Pierluigi