Predictors of Outcome in Clinically Diagnosed Viral Encephalitis Patients: A 5-Year Prospective Study von Wang, Xuefeng, Hu, Yida, Li, Feng, Zhou, Lunqin, Feng, Guibo, Tian, Xin

Volltext

Amyloid fibrils from the N-terminal prion protein fragment are infectious von Choi, Jin-Kyu, Cali, Ignazio, Surewicz, Krystyna, Kong, Qingzhong, Gambetti, Pierluigi, Surewicz, Witold K.

Volltext

Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics von Cali, Ignazio, Puoti, Gianfranco, Smucny, Jason, Curtiss, Paul Michael, Cracco, Laura, Kitamoto, Tetsuyuki, Occhipinti, Rossana, Cohen, Mark Lloyd, Appleby, Brian Stephen, Gambetti, Pierluigi

Volltext

PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study von Cali, Ignazio, Lavrich, Jody, Moda, Fabio, Kofskey, Diane, Nemani, Satish Kumar, Appleby, Brian, Tagliavini, Fabrizio, Soto, Claudio, Gambetti, Pierluigi, Notari, Silvio

Volltext

Mammalian Prions Generated from Bacterially Expressed Prion Protein in the Absence of Any Mammalian Cofactors von Kim, Jae-Il, Cali, Ignazio, Surewicz, Krystyna, Kong, Qingzhong, Raymond, Gregory J., Atarashi, Ryuichiro, Race, Brent, Qing, Liuting, Gambetti, Pierluigi, Caughey, Byron, Surewicz, Witold K.

Volltext

Human prion diseases: surgical lessons learned from iatrogenic prion transmission von Bonda, David J, Manjila, Sunil, Mehndiratta, Prachi, Khan, Fahd, Miller, Benjamin R, Onwuzulike, Kaine, Puoti, Gianfranco, Cohen, Mark L, Schonberger, Lawrence B, Cali, Ignazio

Volltext

Variable Protease-Sensitive Prionopathy Transmission to Bank Voles von Nonno, Romolo, Notari, Silvio, Di Bari, Michele Angelo, Cali, Ignazio, Pirisinu, Laura, d'Agostino, Claudia, Cracco, Laura, Kofskey, Diane, Vanni, Ilaria, Lavrich, Jody, Parchi, Piero, Agrimi, Umberto, Gambetti, Pierluigi

Volltext

Molecular biology and pathology of prion strains in sporadic human prion diseases von Gambetti, Pierluigi, Cali, Ignazio, Notari, Silvio, Kong, Qingzhong, Zou, Wen-Quan, Surewicz, Witold K.

Volltext

Generation of human chronic wasting disease in transgenic mice von Wang, Zerui, Qin, Kefeng, Camacho, Manuel V, Cali, Ignazio, Yuan, Jue, Shen, Pingping, Greenlee, Justin, Kong, Qingzhong, Mastrianni, James A, Zou, Wen-Quan

Volltext

Transmission characteristics of variably protease-sensitive prionopathy von Notari, Silvio, Xiao, Xiangzhu, Espinosa, Juan Carlos, Cohen, Yvonne, Qing, Liuting, Aguilar-Calvo, Patricia, Kofskey, Diane, Cali, Ignazio, Cracco, Laura, Kong, Qingzhong, Torres, Juan Maria, Zou, Wenquan, Gambetti, Pierluigi

Volltext

Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report von Carrasco, Adrianna E, Appleby, Brian S, Cali, Ignazio, Okhravi, Hamid R

Volltext

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics von Cali, Ignazio, Castellani, Rudolph, Alshekhlee, Amer, Cohen, Yvonne, Blevins, Janis, Yuan, Jue, Langeveld, Jan P. M., Parchi, Piero, Safar, Jiri G., Zou, Wen-Quan, Gambetti, Pierluigi

Volltext

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study von Cali, Ignazio, Cohen, Mark L, Haik, Stephane, Parchi, Piero, Giaccone, Giorgio, Collins, Steven J, Kofskey, Diane, Wang, Han, McLean, Catriona A, Brandel, Jean-Philippe, Privat, Nicolas, Sazdovitch, Véronique, Duyckaerts, Charles, Kitamoto, Tetsuyuki, Belay, Ermias D, Maddox, Ryan A, Tagliavini, Fabrizio, Pocchiari, Maurizio, Leschek, Ellen, Appleby, Brian S, Safar, Jiri G, Schonberger, Lawrence B, Gambetti, Pierluigi

Volltext

Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion von Cali, Ignazio, Cracco, Laura, Saracino, Dario, Occhipinti, Rossana, Coppola, Cinzia, Appleby, Brian Stephen, Puoti, Gianfranco

Volltext

Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype von Cracco, Laura, Puoti, Gianfranco, Cornacchia, Antonio, Glisic, Katie, Lee, Seong-Ki, Wang, Zerui, Cohen, Mark L, Appleby, Brian S, Cali, Ignazio

Volltext

Evaluation of the Human Transmission Risk of an Atypical Bovine Spongiform Encephalopathy Prion Strain von QINGZHONG KONG, MENGJIE ZHENG, MARTUCCI, Francesca, IULINI, Barbara, ACUTIS, Pierluigi, LAN WANG, JINGJING LIANG, MEILING WANG, XINYI LI, MONACO, Salvatore, ZANUSSO, Gianluigi, ZOU, Wen-Quan, CASALONE, Cristina, CARAMELLI, Maria, GAMBETTI, Pierluigi, LIUTING QING, SHENGHAI HUANG, CHAKRABORTY, Bikram, PING WANG, FUSONG CHEN, CALI, Ignazio, CORONA, Cristiano

Volltext

Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type von Cracco, Laura, Notari, Silvio, Cali, Ignazio, Sy, Man-Sun, Chen, Shu G., Cohen, Mark L., Ghetti, Bernardino, Appleby, Brian S., Zou, Wen-Quan, Caughey, Byron, Safar, Jiri G., Gambetti, Pierluigi

Volltext

Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification von Baiardi, Simone, Rossi, Marcello, Mammana, Angela, Appleby, Brian S., Barria, Marcelo A., Calì, Ignazio, Gambetti, Pierluigi, Gelpi, Ellen, Giese, Armin, Ghetti, Bernardino, Herms, Jochen, Ladogana, Anna, Mikol, Jacqueline, Pal, Suvankar, Ritchie, Diane L., Ruf, Viktoria, Windl, Otto, Capellari, Sabina, Parchi, Piero

Volltext

Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion von Brennecke, Nicholas, Cali, Ignazio, Mok, Tze How, Speedy, Helen, Genomics England Research Consortium, Hosszu, Laszlo L P, Stehmann, Christiane, Cracco, Laura, Puoti, Gianfranco, Prior, Thomas W, Cohen, Mark L, Collins, Steven J, Mead, Simon, Appleby, Brian S

Volltext

Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments von Cracco, Laura, Xiao, Xiangzhu, Nemani, Satish K, Lavrich, Jody, Cali, Ignazio, Ghetti, Bernardino, Notari, Silvio, Surewicz, Witold K, Gambetti, Pierluigi

Volltext