Cerebrospinal Fluid and Blood Neurofilament Light Chain Protein in Prion Disease and Other Rapidly Progressive Dementias: Current State of the Art

Por Abu-Rumeileh, Samir, Parchi, Piero
Publicado no Front Neurosci (2021)

Prion Protein Misfolding, Strains, and Neurotoxicity: An Update from Studies on Mammalian Prions

Por Poggiolini, Ilaria, Saverioni, Daniela, Parchi, Piero
Publicado em 2013

Understanding Prion Strains: Evidence from Studies of the Disease Forms Affecting Humans

Por Rossi, Marcello, Baiardi, Simone, Parchi, Piero
Publicado no Viruses (2019)

Recent advances in the histo‐molecular pathology of human prion disease

Por Baiardi, Simone, Rossi, Marcello, Capellari, Sabina, Parchi, Piero
Publicado no Brain Pathol (2019)

Wait and see: a 5 year history of ‘recurrent dementia’

Por D'Angelo, Roberto, Rinaldi, Rita, Parchi, Piero, Cirignotta, Fabio
Publicado no BMJ Case Rep (2014)

Towards an improved early diagnosis of neurodegenerative diseases: the emerging role of in vitro conversion assays for protein amyloids

Por Candelise, Niccolò, Baiardi, Simone, Franceschini, Alessia, Rossi, Marcello, Parchi, Piero
Publicado no Acta Neuropathol Commun (2020)

Primary progressive narcolepsy type 1: The other side of the coin

Por Pizza, Fabio, Vandi, Stefano, Liguori, Rocco, Parchi, Piero, Avoni, Patrizia, Mignot, Emmanuel, Plazzi, Giuseppe
Publicado no Neurology (2014)

Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings

Por Baiardi, Simone, Capellari, Sabina, Ladogana, Anna, Strumia, Silvia, Santangelo, Mario, Pocchiari, Maurizio, Parchi, Piero
Publicado no J Alzheimers Dis (2015)

Diagnostic Accuracy of a Combined Analysis of Cerebrospinal Fluid t-PrP, t-tau, p-tau, and Aβ(42) in the Differential Diagnosis of Creutzfeldt-Jakob Disease from Alzheimer’s Diseas...

Por Abu Rumeileh, Samir, Lattanzio, Francesca, Stanzani Maserati, Michelangelo, Rizzi, Romana, Capellari, Sabina, Parchi, Piero
Publicado no J Alzheimers Dis (2016)

Neurofilaments in motor neuron disorders: towards promising diagnostic and prognostic biomarkers

Por Zucchi, Elisabetta, Bonetto, Valentina, Sorarù, Gianni, Martinelli, Ilaria, Parchi, Piero, Liguori, Rocco, Mandrioli, Jessica
Publicado no Mol Neurodegener (2020)

Analyses of Protease Resistance and Aggregation State of Abnormal Prion Protein across the Spectrum of Human Prions

Por Saverioni, Daniela, Notari, Silvio, Capellari, Sabina, Poggiolini, Ilaria, Giese, Armin, Kretzschmar, Hans A., Parchi, Piero
Publicado em 2013

Iodine-123-meta-iodobenzylguanidine Myocardial Scintigraphy in Isolated Autonomic Failure: Potential Red Flag for Future Multiple System Atrophy

Por Baschieri, Francesca, Calandra-Buonaura, Giovanna, Cecere, Annagrazia, Barletta, Giorgio, Contin, Manuela, Parchi, Piero, Cortelli, Pietro
Publicado no Front Neurol (2017)

Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions

Por Cescatti, Maura, Saverioni, Daniela, Capellari, Sabina, Tagliavini, Fabrizio, Kitamoto, Tetsuyuki, Ironside, James, Giese, Armin, Parchi, Piero
Publicado no J Virol (2016)

Detection of prions in skin punch biopsies of Creutzfeldt–Jakob disease patients

Por Mammana, Angela, Baiardi, Simone, Rossi, Marcello, Franceschini, Alessia, Donadio, Vincenzo, Capellari, Sabina, Caughey, Byron, Parchi, Piero
Publicado no Ann Clin Transl Neurol (2020)

Effect of the E200K Mutation on Prion Protein Metabolism : Comparative Study of a Cell Model and Human Brain

Por Capellari, Sabina, Parchi, Piero, Russo, Claudio M., Sanford, Jeremy, Sy, Man-Sun, Gambetti, Pierluigi, Petersen, Robert B.
Publicado em 2000

Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein

Por Race, Brent, Williams, Katie, Hughson, Andrew G., Jansen, Casper, Parchi, Piero, Rozemuller, Annemieke J. M., Chesebro, Bruce
Publicado no Acta Neuropathol Commun (2018)

Gerstmann-Sträussler-Scheinker disease (PRNP p.D202N) presenting with atypical parkinsonism

Por Baiardi, Simone, Rizzi, Romana, Capellari, Sabina, Bartoletti-Stella, Anna, Zangrandi, Andrea, Gasparini, Federico, Ghidoni, Enrico, Parchi, Piero
Publicado no Neurol Genet (2020)

CSF Ubiquitin Levels Are Higher in Alzheimer’s Disease than in Frontotemporal Dementia and Reflect the Molecular Subtype in Prion Disease

Por Abu-Rumeileh, Samir, Oeckl, Patrick, Baiardi, Simone, Halbgebauer, Steffen, Steinacker, Petra, Capellari, Sabina, Otto, Markus, Parchi, Piero
Publicado no Biomolecules (2020)

Transmission Properties of Atypical Creutzfeldt-Jakob Disease: a Clue to Disease Etiology?

Por Kobayashi, Atsushi, Parchi, Piero, Yamada, Masahito, Brown, Paul, Saverioni, Daniela, Matsuura, Yuichi, Takeuchi, Atsuko, Mohri, Shirou, Kitamoto, Tetsuyuki
Publicado no J Virol (2015)

An in vivo (11)C‐PK PET study of microglia activation in Fatal Familial Insomnia

Por Iaccarino, Leonardo, Presotto, Luca, Bettinardi, Valentino, Gianolli, Luigi, Roiter, Ignazio, Capellari, Sabina, Parchi, Piero, Cortelli, Pietro, Perani, Daniela
Publicado no Ann Clin Transl Neurol (2017)