30 Publications (Page 1 of 2)
2020
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics.
I, Cali⋅G, Puoti⋅J, Smucny⋅PM, Curtiss⋅L, Cracco⋅T, Kitamoto⋅R, Occhipinti⋅ML, Cohen⋅BS, Appleby and P, Gambetti
Scientific reports. | Journal Article
2019
Covalently-linked PrP fragments in two major GSS variants. Prion 2019
 
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments.
Cracco, Laura⋅L, Cracco⋅X, Xiao⋅Xiao, Xiangzhu⋅SK, Nemani⋅Nemani, Satish K⋅Lavrich, Jody⋅J, Lavrich⋅Cali, Ignazio⋅I, Cali⋅Ghetti, Bernardino⋅B, Ghetti⋅S, Notari⋅Notari, Silvio⋅Surewicz, Witold K⋅WK, Surewicz⋅P, Gambetti and Gambetti, Pierluigi
Acta neuropathologica communications. | Journal Article
 
Variable Protease-Sensitive Prionopathy Transmission to Bank Voles.
R, Nonno⋅S, Notari⋅MA, Di Bari⋅I, Cali⋅L, Pirisinu⋅C⋅L, Cracco⋅D, Kofskey⋅I, Vanni⋅J, Lavrich⋅P, Parchi⋅U, Agrimi and P, Gambetti
Emerging infectious diseases. | Journal Article
2018
Fatal familial insomnia and sporadic fatal insomnia.
Cracco, Laura⋅L, Cracco⋅BS, Appleby⋅Appleby, Brian S⋅Gambetti, Pierluigi and P, Gambetti
Handbook of clinical neurology. | Journal Article
2017
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type.
L, Cracco⋅Cracco, Laura⋅S, Notari⋅Notari, Silvio⋅I, Cali⋅Cali, Ignazio⋅Sy, Man Sun⋅MS, Sy⋅Chen, Shu G⋅SG, Chen⋅ML, Cohen⋅Cohen, Mark L⋅B, Ghetti⋅Ghetti, Bernardino⋅Appleby, Brian S⋅BS, Appleby⋅Zou, Wen Quan⋅WQ, Zou⋅Caughey, Byron⋅B, Caughey⋅Safar, Jiri G⋅JG, Safar⋅Gambetti, Pierluigi and P, Gambetti
Scientific reports. | Journal Article
 
The comparative study of protease-resistant prion protein typically associated with CJD and GSS reveals an unexpected basic similarity. Ninety-third Annual Meeting of the American Association of Neuropathologists
 
Transmission study of human prion diseases in PrP glycan-KO transgenic mice. prion 2017
2015
New determinants of phenotypic diversity in sporadic human prion diseases. Prion 2015
 
Synthetic Aβ peptides acquire prion-like properties in the brain.
X, Xiao⋅Xiao, Xiangzhu⋅Cali, Ignazio⋅I, Cali⋅J, Yuan⋅Yuan, Jue⋅L, Cracco⋅Cracco, Laura⋅Curtiss, Paul⋅P, Curtiss⋅L, Zeng⋅Zeng, Liang⋅Abouelsaad, Mai⋅M, Abouelsaad⋅D, Gazgalis⋅Gazgalis, Dimitris⋅GX, Wang⋅Wang, Gong-Xian⋅Kong, Qingzhong⋅Q, Kong⋅H, Fujioka⋅Fujioka, Hisashi⋅Puoti, Gianfranco⋅G, Puoti⋅WQ, Zou and Zou, Wen Quan
Oncotarget. | Journal Article
2014
Genetic Creutzfeldt–Jakob disease associated with the P105S-129V mutation in the PRNP gene. XVIII International Congress of Neuropathology
 
Glycans modulate the transmissibility of PrPSc and the sCJDMM2 and sFI phenotypes. Ninetieth Annual Meeting of the American Association of Neuropathologists
 
Sporadic fatal insomnia in an adolescent.
JL, Blase⋅L, Cracco⋅LB, Schonberger⋅RA, Maddox⋅Y, Cohen⋅I, Cali and ED, Belay
Pediatrics. | Journal Article
 
Transmissibility and propagation of co-existing prions of sporadic Creutzfeldt-Jakob disease into humanized transgenic mice. Ninetieth Annual Meeting of the American Association of Neuropathologists
 
Transmissibility and propagation of PrPSc from sCJDMM1-2 in humanized transgenic mice. Prion 2014
 
Transmission characteristics of variably protease-sensitive prionopathy.
S, Notari⋅Notari, Silvio⋅X, Xiao⋅Xiao, Xiangzhu⋅Espinosa, Juan Carlos⋅JC, Espinosa⋅Y, Cohen⋅Cohen, Yvonne⋅Qing, Liuting⋅L, Qing⋅P, Aguilar-Calvo⋅Aguilar-Calvo, Patricia⋅D, Kofskey⋅Kofskey, Diane⋅Cali, Ignazio⋅I, Cali⋅Cracco, Laura⋅L, Cracco⋅Kong, Qingzhong⋅Q, Kong⋅Torres, Juan Maria⋅JM, Torres⋅Zou, Wenquan⋅W, Zou⋅Gambetti, Pierluigi and P, Gambetti
Emerging infectious diseases. | Journal Article
2013
A case of Creutzfeldt-Jakob disease associated with the P105S-129V mutation in PRNP gene. Eighty Ninth Annual Meeting of the American Association of Neuropathologists
 
Co-occurrence of distinct types of scrapie prion protein in sporadic Creutzfeldt- Jakob disease. Eighty Ninth Annual Meeting of the American Association of Neuropathologists
 
Heart-fatty acid-binding and tau proteins relate to brain injury severity and long-term outcome in subarachnoid haemorrhage patients.
ER, Zanier⋅T, Zoerle⋅M, Fiorini⋅L, Longhi⋅L, Cracco⋅A, Bersano⋅V, Branca⋅MD, Benedetti⋅MG, De Simoni⋅S, Monaco and N, Stocchetti
British journal of anaesthesia. | Journal Article
 
New mechanisms of phenotypic determination in sporadic Creutzfeldt-Jakob disease and sporadic fatal insomnia. Eighty Ninth Annual Meeting of the American Association of Neuropathologists
2012
Analysis of phenotypic heterogeneity associated with homologous genotype-PrPSc type pairings: sCJDMV2, sCJDMM2 and sFI. Prion 2012
 
Co-existence of PrPSc types 1 and 2 in sporadic CJD with genotype 129VV. Prion 2012
2011
Phenotypic heterogeneity in Creutzfeldt-Jakob disease associated with a new prion protein mutation. Congress of the Italian Association of Neuropathology (AINP) and XXXVII Congress of the Italian Association for Research on Brain Aging (AIRIC)
 
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report.
KM, Moody⋅Moody, Karen⋅Schonberger, Lawrence⋅LB, Schonberger⋅Maddox, Ryan⋅RA, Maddox⋅Zou, Wen Quan⋅WQ, Zou⋅L, Cracco⋅Cracco, Laura⋅I, Cali and Cali, Ignazio
BMC neurology. | Journal Article
2010
Phenotypic heterogeneity and type-1/2 PrPSc co-occurrence in Creutzfeldt-Jakob disease associated with a new mutation of PRNP. Eighty Sixth Annual Meeting of the American Association of Neuropathologists