Clinical Use of Improved Diagnostic Testing for Detection of Prion Disease

por Figgie, Mark P., Appleby, Brian S.
Publicado 2021

Genetic aspects of human prion diseases

por Appleby, Brian S., Shetty, Shashirekha, Elkasaby, Mohamed
Publicado 2022

A case report of genetic prion disease with two different PRNP variants

por Piazza, Megan, Prior, Thomas W., Khalsa, Prabhjot S., Appleby, Brian
Publicado 2020

Atypical Case of VV1 Creutzfeldt–Jakob Disease Subtype: Case Report

por Carrasco, Adrianna E., Appleby, Brian S., Cali, Ignazio, Okhravi, Hamid R.
Publicado 2022

Racial and Ethnic Differences in Individuals with Sporadic Creutzfeldt-Jakob Disease in the United States of America

por Appleby, Brian S., Rincon-Beardsley, Tonya D., Appleby, Kristin K., Wallin, Mitchell T.
Publicado 2012

Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion

por Cali, Ignazio, Cracco, Laura, Saracino, Dario, Occhipinti, Rossana, Coppola, Cinzia, Appleby, Brian Stephen, Puoti, Gianfranco
Publicado 2020

Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species

por Osterholm, Michael T., Anderson, Cory J., Zabel, Mark D., Scheftel, Joni M., Moore, Kristine A., Appleby, Brian S.
Publicado 2019

Prevalence of Surgical Procedures at Symptomatic Onset of Prion Disease

por Porter, Amanda L., Prusinski, Christian C., Lazar, Evelyn, Yuh, Clara, Bucelli, Robert C., Appleby, Brian S., Day, Gregory S.
Publicado 2022

Iatrogenic Creutzfeldt-Jakob Disease from Commercial Cadaveric Human Growth Hormone

por Appleby, Brian S., Lu, Mei, Bizzi, Alberto, Phillips, Michael D., Berri, Sally M., Harbison, Madeleine D., Schonberger, Lawrence B.
Publicado 2013

Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype

por Cracco, Laura, Puoti, Gianfranco, Cornacchia, Antonio, Glisic, Katie, Lee, Seong‑Ki, Wang, Zerui, Cohen, Mark L., Appleby, Brian S., Cali, Ignazio
Publicado 2023

PMCA-replicated PrP(D) in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP(D): Transmission study

por Cali, Ignazio, Lavrich, Jody, Moda, Fabio, Kofskey, Diane, Nemani, Satish Kumar, Appleby, Brian, Tagliavini, Fabrizio, Soto, Claudio, Gambetti, Pierluigi, Notari, Silvio
Publicado 2019

Co-existence of PrP(D) types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics

por Cali, Ignazio, Puoti, Gianfranco, Smucny, Jason, Curtiss, Paul Michael, Cracco, Laura, Kitamoto, Tetsuyuki, Occhipinti, Rossana, Cohen, Mark Lloyd, Appleby, Brian Stephen, Gambetti, Pierluigi
Publicado 2020

Impaired transmissibility of atypical prions from genetic CJD(G114V)

por Cali, Ignazio, Mikhail, Fadi, Qin, Kefeng, Gregory, Crystal, Solanki, Ani, Martinez, Manuel Camacho, Zhao, Lili, Appleby, Brian, Gambetti, Pierluigi, Norstrom, Eric, Mastrianni, James A.
Publicado 2018

Two distinct conformers of PrP(D) type 1 of sporadic Creutzfeldt–Jakob disease with codon 129VV genotype faithfully propagate in vivo

por Cali, Ignazio, Espinosa, Juan Carlos, Nemani, Satish K., Marin-Moreno, Alba, Camacho, Manuel V., Aslam, Rabail, Kitamoto, Tetsuyuki, Appleby, Brian S., Torres, Juan Maria, Gambetti, Pierluigi
Publicado 2021

Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases

por Pirisinu, Laura, Di Bari, Michele A., D’Agostino, Claudia, Marcon, Stefano, Riccardi, Geraldina, Poleggi, Anna, Cohen, Mark L., Appleby, Brian S., Gambetti, Pierluigi, Ghetti, Bernardino, Agrimi, Umberto, Nonno, Romolo
Publicado 2016

Co-occurrence of chronic traumatic encephalopathy and prion disease

por Nemani, Satish Kumar, Notari, Silvio, Cali, Ignazio, Alvarez, Victor E, Kofskey, Diane, Cohen, Mark, Stern, Robert A., Appleby, Brian, Abrams, Joseph, Schonberger, Lawrence, McKee, Ann, Gambetti, Pierluigi
Publicado 2018

Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type

por 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
Publicado 2017

Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease

por Pascuzzo, Riccardo, Oxtoby, Neil P., Young, Alexandra L., Blevins, Janis, Castelli, Gianmarco, Garbarino, Sara, Cohen, Mark L., Schonberger, Lawrence B., Gambetti, Pierluigi, Appleby, Brian S., Alexander, Daniel C., Bizzi, Alberto
Publicado 2020

A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease

por 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
Publicado 2020

Subtype Diagnosis of Sporadic Creutzfeldt–Jakob Disease with Diffusion Magnetic Resonance Imaging

por Bizzi, Alberto, Pascuzzo, Riccardo, Blevins, Janis, Moscatelli, Marco E. M., Grisoli, Marina, Lodi, Raffaele, Doniselli, Fabio M., Castelli, Gianmarco, Cohen, Mark L., Stamm, Aymeric, Schonberger, Lawrence B., Appleby, Brian S., Gambetti, Pierluigi
Publicado 2020