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 2021

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

por Poggiolini, Ilaria, Saverioni, Daniela, Parchi, Piero
Publicado 2013

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

por Rossi, Marcello, Baiardi, Simone, Parchi, Piero
Publicado 2019

The Use of Real-Time Quaking-Induced Conversion for the Diagnosis of Human Prion Diseases

por Poleggi, Anna, Baiardi, Simone, Ladogana, Anna, Parchi, Piero
Publicado 2022

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 2020

The First Sporadic Creutzfeldt–Jakob Disease Case with a Rare Molecular Subtype VV1 and 1-Octapeptide Repeat Deletion in PRNP

por Areškevičiūtė, Aušrinė, Lund, Eva Løbner, Capellari, Sabina, Parchi, Piero, Pinkowsky, Christian Tersbøl
Publicado 2021

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 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 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 2020

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 2017

Genomic, transcriptomic and RNA editing analysis of human MM1 and VV2 sporadic Creutzfeldt-Jakob disease

por Tarozzi, Martina, Baiardi, Simone, Sala, Claudia, Bartoletti-Stella, Anna, Parchi, Piero, Capellari, Sabina, Castellani, Gastone
Publicado 2022

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 2020

RT‐QuIC Detection of Pathological α‐Synuclein in Skin Punches of Patients with Lewy Body Disease

por Mammana, Angela, Baiardi, Simone, Quadalti, Corinne, Rossi, Marcello, Donadio, Vincenzo, Capellari, Sabina, Liguori, Rocco, Parchi, Piero
Publicado 2021

Phenotypic Heterogeneity of Variably Protease-Sensitive Prionopathy: A Report of Three Cases Carrying Different Genotypes at PRNP Codon 129

por Baiardi, Simone, Mammana, Angela, Rossi, Marcello, Ladogana, Anna, Carlà, Benedetta, Gambetti, Pierluigi, Capellari, Sabina, Parchi, Piero
Publicado 2022

Diagnostic and prognostic value of cerebrospinal fluid SNAP-25 and neurogranin in Creutzfeldt-Jakob disease in a clinical setting cohort of rapidly progressive dementias

por Bentivenga, Giuseppe Mario, Baiardi, Simone, Mastrangelo, Andrea, Zenesini, Corrado, Mammana, Angela, Polischi, Barbara, Capellari, Sabina, Parchi, Piero
Publicado 2023

Kinetic parameters of alpha-synuclein seed amplification assay correlate with cognitive impairment in patients with Lewy body disorders

por Bräuer, Stefan, Rossi, Marcello, Sajapin, Johann, Henle, Thomas, Gasser, Thomas, Parchi, Piero, Brockmann, Kathrin, Falkenburger, Björn H.
Publicado 2023

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 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 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 2020

Frequency of Parkinson’s Disease Genes and Role of PARK2 in Amyotrophic Lateral Sclerosis: An NGS Study

por Vacchiano, Veria, Bartoletti-Stella, Anna, Rizzo, Giovanni, Avoni, Patrizia, Parchi, Piero, Salvi, Fabrizio, Liguori, Rocco, Capellari, Sabina
Publicado 2022