Works by Parchi, Piero

Results: 155

Alpha-synuclein seed amplification assay longitudinal outcomes in Lewy body disease spectrum.

Published in:

Brain: A Journal of Neurology, 2025, v. 148, n. 6, p. 2038, doi. 10.1093/brain/awae405

By:

Mastrangelo, Andrea;
Mammana, Angela;
Hall, Sara;
Stomrud, Erik;
Zenesini, Corrado;
Rossi, Marcello;
Janelidze, Shorena;
Ticca, Alice;
Palmqvist, Sebastian;
Magliocchetti, Franco;
Baiardi, Simone;
Mattsson-Carlgren, Niklas;
Hansson, Oskar;
Parchi, Piero

Publication type:

Article

Clinical use and reporting of neurofilament quantification in neurological disorders: A global overview.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2025, v. 21, n. 6, p. 1, doi. 10.1002/alz.70343

By:

Delaby, Constance;
Ladang, Aurélie;
Martinez‐Yriarte, Jose;
Zecca, Chiara;
Logroscino, Giancarlo;
Körtvelyessy, Peter;
Tumani, Hayrettin;
Parchi, Piero;
Quadrio, Isabelle;
Hart, Melanie;
Olsen, Dorte Aalund;
Alcolea, Daniel;
Blennow, Kaj;
Fortea, Juan;
Lleo, Alberto;
Algeciras‐Schimnich, Alicia;
Ayrignac, Xavier;
Bedel, Aurélie;
Santos, Gustavo A. A.;
Borelli, Wyllians

Publication type:

Article

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

Published in:

Viruses (1999-4915), 2022, v. 14, n. 2, p. 367, doi. 10.3390/v14020367

By:

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

Publication type:

Article

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

Published in:

2021

By:

Areškevičiūtė, Aušrinė;
Lund, Eva Løbner;
Capellari, Sabina;
Parchi, Piero;
Pinkowsky, Christian Tersbøl

Publication type:

Case Study

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

Published in:

Viruses (1999-4915), 2019, v. 11, n. 4, p. 309, doi. 10.3390/v11040309

By:

Rossi, Marcello;
Baiardi, Simone;
Parchi, Piero

Publication type:

Article

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

Published in:

Frontiers in Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fnins.2021.648743

By:

Abu-Rumeileh, Samir;
Parchi, Piero

Publication type:

Article

A comparison of p‐tau assays for the specificity to detect tau changes in Alzheimer's disease.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2025, v. 21, n. 4, p. 1, doi. 10.1002/alz.70208

By:

Janelidze, Shorena;
Ashton, Nicholas J.;
Orduña Dolado, Anna;
Nordström, Ulrika;
Bali, Divya;
Forsberg, Karin M. E.;
Keskin, Isil;
Mastrangelo, Andrea;
Vacchiano, Veria;
Liguori, Rocco;
Blennow, Kaj;
Zetterberg, Henrik;
Mattsson‐Carlgren, Niklas;
Gonzalez‐Ortiz, Fernando;
Parchi, Piero;
Andersen, Peter Munch;
Hansson, Oskar

Publication type:

Article

Clinical value of novel blood‐based tau biomarkers in Creutzfeldt–Jakob disease.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2025, v. 21, n. 2, p. 1, doi. 10.1002/alz.14422

By:

Bentivenga, Giuseppe Mario;
Gonzalez‐Ortiz, Fernando;
Baiardi, Simone;
Kirsebom, Bjørn‐Eivind;
Mastrangelo, Andrea;
Mammana, Angela;
Capellari, Sabina;
Fladby, Tormod;
Zetterberg, Henrik;
Blennow, Kaj;
Parchi, Piero

Publication type:

Article

The MRI signature of alpha‐synuclein pathology in preclinical stages and in a memory clinic population.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. S2, p. 1, doi. 10.1002/alz.088839

By:

Wisse, Laura E.M.;
Spotorno, Nicola;
Strandberg, Olof;
van Westen, Danielle;
Mattsson‐Carlgren, Niklas;
Palmqvist, Sebastian;
Stomrud, Erik;
Parchi, Piero;
Hansson, Oskar

Publication type:

Article

Associations between misfolded alpha‐synuclein aggregates and Alzheimer's disease pathology in vivo.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 11, p. 7624, doi. 10.1002/alz.14225

By:

Pichet Binette, Alexa;
Mammana, Angela;
Wisse, Laura;
Rossi, Marcello;
Strandberg, Olof;
Smith, Ruben;
Mattsson‐Carlgren, Niklas;
Janelidze, Shorena;
Palmqvist, Sebastian;
Ticca, Alice;
Stomrud, Erik;
Parchi, Piero;
Hansson, Oskar

Publication type:

Article

In vivo detection of Alzheimer's and Lewy body disease concurrence: Clinical implications and future perspectives.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 8, p. 5757, doi. 10.1002/alz.14039

By:

Baiardi, Simone;
Hansson, Oskar;
Levin, Johannes;
Parchi, Piero

Publication type:

Article

Levels of plasma brain‐derived tau and p‐tau181 in Alzheimer's disease and rapidly progressive dementias.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 1, p. 745, doi. 10.1002/alz.13516

By:

Gonzalez‐Ortiz, Fernando;
Karikari, Thomas K.;
Bentivenga, Giuseppe Mario;
Baiardi, Simone;
Mammana, Angela;
Turton, Michael;
Kac, Przemysław R.;
Mastrangelo, Andrea;
Harrison, Peter;
Capellari, Sabina;
Zetterberg, Henrik;
Blennow, Kaj;
Parchi, Piero

Publication type:

Article

Duodenal alpha‐Synuclein Pathology and Enteric Gliosis in Advanced Parkinson's Disease.

Published in:

Movement Disorders, 2023, v. 38, n. 5, p. 885, doi. 10.1002/mds.29358

By:

Emmi, Aron;
Sandre, Michele;
Russo, Francesco Paolo;
Tombesi, Giulia;
Garrì, Federica;
Campagnolo, Marta;
Carecchio, Miryam;
Biundo, Roberta;
Spolverato, Gaya;
Macchi, Veronica;
Savarino, Edoardo;
Farinati, Fabio;
Parchi, Piero;
Porzionato, Andrea;
Bubacco, Luigi;
De Caro, Raffaele;
Kovacs, Gabor G.;
Antonini, Angelo

Publication type:

Article

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

Published in:

Movement Disorders, 2021, v. 36, n. 9, p. 2173, doi. 10.1002/mds.28651

By:

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

Publication type:

Article

Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation.

Published in:

2017

By:

Terlizzi, Rossana;
Valentino, Maria Lucia;
Bartoletti‐Stella, Anna;
Columbaro, Marta;
Piras, Silvia;
Stanzani‐Maserati, Michelangelo;
Quadri, Marialuisa;
Breedveld, Guido J.;
Bonifati, Vincenzo;
Martinelli, Paolo;
Parchi, Piero;
Capellari, Sabina;
Bartoletti-Stella, Anna;
Stanzani-Maserati, Michelangelo

Publication type:

Case Study

Gait disorders in fatal familial insomnia.

Published in:

Movement Disorders, 2014, v. 29, n. 3, p. 420, doi. 10.1002/mds.25786

By:

Cortelli, Pietro;
Fabbri, Margherita;
Calandra‐Buonaura, Giovanna;
Capellari, Sabina;
Tinuper, Paolo;
Parchi, Piero;
Lugaresi, Elio

Publication type:

Article

MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome.

Published in:

Movement Disorders, 2007, v. 22, n. 6, p. 898, doi. 10.1002/mds.21426

By:

Magherini, Anna;
Pentore, Roberta;
Galassi, Giuliana;
Stucchi, Carlo M.;
Capellari, Sabina;
Parchi, Piero

Publication type:

Article

Rapidly progressive multiple system atrophy in a patient carrying LRRK2 G2019S mutation.

Published in:

Neurological Sciences, 2024, v. 45, n. 1, p. 309, doi. 10.1007/s10072-023-07056-5

By:

Carrer, Tommaso;
Bonato, Giulia;
Sandre, Michele;
Emmi, Aron;
Campagnolo, Marta;
Musso, Giulia;
Carecchio, Miryam;
Parchi, Piero;
Antonini, Angelo

Publication type:

Article

An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.

Published in:

Neurological Sciences, 2010, v. 31, n. 6, p. 837, doi. 10.1007/s10072-010-0388-0

By:

Masullo, Carlo;
Bizzarro, Alessandra;
Guglielmi, Valeria;
Iannaccone, Elisabetta;
Minicuci, Giacomo;
Vita, Maria Gabriella;
Capellari, Sabina;
Parchi, Piero;
Servidei, Serenella

Publication type:

Article

Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.

Published in:

2009

By:

Mancuso M;
Siciliano G;
Capellari S;
Orsucci D;
Moretti P;
Fede GD;
Suardi S;
Strammiello R;
Parchi P;
Tagliavini F;
Murri L;
Mancuso, Michelangelo;
Siciliano, Gabriele;
Capellari, Sabina;
Orsucci, Daniele;
Moretti, Policarpo;
Di Fede, Giuseppe;
Suardi, Silvia;
Strammiello, Rosaria;
Parchi, Piero

Publication type:

journal article

Creutzfeldt–Jakob disease with E200K PRNP mutation: a case report and revision of the literature.

Published in:

Neurological Sciences, 2009, v. 30, n. 5, p. 417, doi. 10.1007/s10072-009-0118-7

By:

Mancuso, Michelangelo;
Siciliano, Gabriele;
Capellari, Sabina;
Orsucci, Daniele;
Moretti, Policarpo;
Fede, Giuseppe;
Suardi, Silvia;
Strammiello, Rosaria;
Parchi, Piero;
Tagliavini, Fabrizio;
Murri, Luigi

Publication type:

Article

MRI Signature of α-Synuclein Pathology in Asymptomatic Stages and a Memory Clinic Population.

Published in:

JAMA Neurology, 2024, v. 81, n. 10, p. 1051, doi. 10.1001/jamaneurol.2024.2713

By:

Wisse, Laura E. M.;
Spotorno, Nicola;
Rossi, Marcello;
Grothe, Michel J.;
Mammana, Angela;
Tideman, Pontus;
Baiardi, Simone;
Strandberg, Olof;
Ticca, Alice;
van Westen, Danielle;
Mattsson-Carlgren, Niklas;
Palmqvist, Sebastian;
Stomrud, Erik;
Parchi, Piero;
Hansson, Oskar

Publication type:

Article

Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma.

Published in:

Neuropathology, 2017, v. 37, n. 2, p. 110, doi. 10.1111/neup.12343

By:

Vita, Maria Gabriella;
Tiple, Dorina;
Bizzarro, Alessandra;
Ladogana, Anna;
Colaizzo, Elisa;
Capellari, Sabina;
Rossi, Marcello;
Parchi, Piero;
Masullo, Carlo;
Pocchiari, Maurizio

Publication type:

Article

Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.

Published in:

Neuropathology, 2016, v. 36, n. 3, p. 305, doi. 10.1111/neup.12270

By:

Kobayashi, Atsushi;
Parchi, Piero;
Yamada, Masahito;
Mohri, Shirou;
Kitamoto, Tetsuyuki

Publication type:

Article

Atypical neuropathological sCJD-MM phenotype with abundant white matter Kuru-type plaques sparing the cerebellar cortex.

Published in:

Neuropathology, 2013, v. 33, n. 2, p. 204, doi. 10.1111/j.1440-1789.2012.01341.x

By:

Gelpi, Ellen;
Soler Insa, Josep Ma;
Parchi, Piero;
Saverioni, Daniela;
Yagüe, Jordi;
Nos, Carlos;
Martínez‐ Saez, Elena;
Ribalta, Teresa;
Ferrer, Isidre;
Sanchez‐Valle, Raquel

Publication type:

Article

Duodenal alpha-Synuclein pathology and enteric gliosis in advanced Parkinson’s Disease patients.

Published in:

Italian Journal of Anatomy & Embryology / Archivio Italiano di Anatomia Ed Embriologia, 2022, v. 126, p. 225

By:

Emmi, Aron;
Sandre, Michele;
Russo, Francesco Paolo;
Tombesi, Giulia;
Garrì, Federica;
Campagnolo, Marta;
Carecchio, Miryam;
Biundo, Roberta;
Spolverato, Gaya;
Macchi, Veronica;
Savarino, Edoardo;
Farinati, Fabio;
Parchi, Piero;
Porzionato, Andrea;
Bubacco, Luigi;
De Caro, Raffaele;
Kovacs, Gabor G.;
Antonini, Angelo

Publication type:

Article

Improving protocols for α-synuclein seed amplification assays: analysis of preanalytical and analytical variables and identification of candidate parameters for seed quantification.

Published in:

Clinical Chemistry & Laboratory Medicine, 2024, v. 62, n. 10, p. 2001, doi. 10.1515/cclm-2023-1472

By:

Mammana, Angela;
Baiardi, Simone;
Rossi, Marcello;
Quadalti, Corinne;
Ticca, Alice;
Magliocchetti, Franco;
Bernhardt, Alexander;
Capellari, Sabina;
Parchi, Piero

Publication type:

Article

Sporadic and familial CJD: classification and characterisation.

Published in:

British Medical Bulletin, 2003, v. 66, n. 1, p. 213, doi. 10.1093/bmb/66.1.213

By:

Pierluigi Gambetti;
Qingzhong Kong;
Wenquan Zou;
Piero Parchi;
Shu G Chen

Publication type:

Article

Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.

Published in:

Microscopy Research & Technique, 2000, v. 50, n. 1, p. 16, doi. 10.1002/1097-0029(20000701)50:1<16::AID-JEMT4>3.0.CO;2-Y

By:

Parchi, Piero;
Capellari, Sabina;
Gambetti, Pierluigi

Publication type:

Article

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

Published in:

Brain Pathology, 2019, v. 29, n. 2, p. 278, doi. 10.1111/bpa.12695

By:

Baiardi, Simone;
Rossi, Marcello;
Capellari, Sabina;
Parchi, Piero

Publication type:

Article

Inter-Laboratory Assessment of PrP<sup>Sc</sup> Typing in Creutzfeldt–Jakob Disease: A Western Blot Study within the NeuroPrion Consortium.

Published in:

Brain Pathology, 2009, v. 19, n. 3, p. 384, doi. 10.1111/j.1750-3639.2008.00187.x

By:

Parchi, Piero;
Notari, Silvio;
Weber, Petra;
Schimmel, Heinz;
Budka, Herbert;
Ferrer, Isidre;
Haik, Stéphane;
Hauw, Jean-Jacques;
WHead, Mark;
Ironside, James W.;
Limido, Lucia;
Rodriguez, Agustin;
Ströbel, Thomas;
Tagliavini, Fabrizio;
Kretzschmar, Hans A.

Publication type:

Article

Effects of Formalin Fixation, Paraffin Embedding, and Time of Storage on DNA Preservation in Brain Tissue: A BrainNet Europe Study.

Published in:

Brain Pathology, 2007, v. 17, n. 3, p. 297, doi. 10.1111/j.1750-3639.2007.00073.x

By:

Ferrer, Isidre;
Armstrong, Judith;
Capellari, Sabina;
Parchi, Piero;
Arzberger, Thomas;
Bell, Jeanne;
Budka, Herbert;
Ströbel, Thomas;
Giaccone, Giorgio;
Rossi, Giacomina;
Bogdanovic, Nenad;
Fakai, Peter;
Schmitt, Andrea;
Riederers, Peter;
Al-Sarraj, Safa;
Ravid, Rivka;
Kretzschmar, Hans

Publication type:

Article

Linking the phenotype of SNCA Triplication with PET-MRI imaging pattern and alpha-synuclein CSF seeding.

Published in:

NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00379-8

By:

Wurster, Isabel;
Quadalti, Corinne;
Rossi, Marcello;
Hauser, Ann-Kathrin;
Deuschle, Christian;
Schulte, Claudia;
Waniek, Katharina;
Lachmann, Ingolf;
la Fougere, Christian;
Doppler, Kathrin;
Gasser, Thomas;
Bender, Benjamin;
Parchi, Piero;
Brockmann, Kathrin

Publication type:

Article

Neurofilament light chain and α-synuclein RT-QuIC as differential diagnostic biomarkers in parkinsonisms and related syndromes.

Published in:

NPJ Parkinson's Disease, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41531-021-00232-4

By:

Quadalti, Corinne;
Calandra-Buonaura, Giovanna;
Baiardi, Simone;
Mastrangelo, Andrea;
Rossi, Marcello;
Zenesini, Corrado;
Giannini, Giulia;
Candelise, Niccolò;
Sambati, Luisa;
Polischi, Barbara;
Plazzi, Giuseppe;
Capellari, Sabina;
Cortelli, Pietro;
Parchi, Piero

Publication type:

Article

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

Published in:

Frontiers in Neurology, 2017, p. 1, doi. 10.3389/fneur.2017.00225

By:

Baschieri, Francesca;
Calandra-Buonaura, Giovanna;
Cecere, Annagrazia;
Barletta, Giorgio;
Contin, Manuela;
Parchi, Piero;
Cortelli, Pietro

Publication type:

Article

Plasma and CSF Neurofilament Light Chain in Amyotrophic Lateral Sclerosis: A Cross-Sectional and Longitudinal Study.

Published in:

Frontiers in Aging Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnagi.2021.753242

By:

Vacchiano, Veria;
Mastrangelo, Andrea;
Zenesini, Corrado;
Masullo, Marco;
Quadalti, Corinne;
Avoni, Patrizia;
Polischi, Barbara;
Cherici, Arianna;
Capellari, Sabina;
Salvi, Fabrizio;
Liguori, Rocco;
Parchi, Piero

Publication type:

Article

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

Published in:

Genes, 2022, v. 13, n. 8, p. 1306, doi. 10.3390/genes13081306

By:

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

Publication type:

Article

Diagnostic and Prognostic Value of Plasma GFAP in Sporadic Creutzfeldt–Jakob Disease in the Clinical Setting of Rapidly Progressive Dementia.

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 10, p. 5106, doi. 10.3390/ijms25105106

By:

Bentivenga, Giuseppe Mario;
Baiardi, Simone;
Mastrangelo, Andrea;
Zenesini, Corrado;
Mammana, Angela;
Rossi, Marcello;
Polischi, Barbara;
Capellari, Sabina;
Parchi, Piero

Publication type:

Article

Amyloid-Beta Co-Pathology Is a Major Determinant of the Elevated Plasma GFAP Values in Amyotrophic Lateral Sclerosis.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 18, p. 13976, doi. 10.3390/ijms241813976

By:

Mastrangelo, Andrea;
Vacchiano, Veria;
Zenesini, Corrado;
Ruggeri, Edoardo;
Baiardi, Simone;
Cherici, Arianna;
Avoni, Patrizia;
Polischi, Barbara;
Santoro, Francesca;
Capellari, Sabina;
Liguori, Rocco;
Parchi, Piero

Publication type:

Article

Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease.

Published in:

International Journal of Molecular Sciences, 2022, v. 23, n. 4, p. 2051, doi. 10.3390/ijms23042051

By:

Abu-Rumeileh, Samir;
Barschke, Peggy;
Oeckl, Patrick;
Baiardi, Simone;
Mammana, Angela;
Mastrangelo, Andrea;
Al Shweiki, Mhd Rami;
Steinacker, Petra;
Ladogana, Anna;
Capellari, Sabina;
Otto, Markus;
Parchi, Piero

Publication type:

Article

Early onset sleep disorders predict severity, progression and death in multiple system atrophy.

Published in:

Journal of Neurology, 2025, v. 272, n. 3, p. 1, doi. 10.1007/s00415-025-12969-6

By:

Giannini, Giulia;
Baldelli, Luca;
Provini, Federica;
Cani, Ilaria;
Baiardi, Simone;
Sambati, Luisa;
Magliocchetti, Franco;
Guaraldi, Pietro;
Parchi, Piero;
Cortelli, Pietro;
Calandra-Buonaura, Giovanna

Publication type:

Article

Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum.

Published in:

Journal of Neurology, 2021, v. 268, n. 10, p. 3766, doi. 10.1007/s00415-021-10521-w

By:

Bartoletti-Stella, Anna;
Vacchiano, Veria;
De Pasqua, Silvia;
Mengozzi, Giacomo;
De Biase, Dario;
Bartolomei, Ilaria;
Avoni, Patrizia;
Rizzo, Giovanni;
Parchi, Piero;
Donadio, Vincenzo;
Chiò, Adriano;
Pession, Annalisa;
Oppi, Federico;
Salvi, Fabrizio;
Liguori, Rocco;
Capellari, Sabina

Publication type:

Article

Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis.

Published in:

Journal of Neurology, 2020, v. 267, n. 6, p. 1699, doi. 10.1007/s00415-020-09761-z

By:

Abu-Rumeileh, Samir;
Vacchiano, Veria;
Zenesini, Corrado;
Polischi, Barbara;
de Pasqua, Silvia;
Fileccia, Enrico;
Mammana, Angela;
Di Stasi, Vitantonio;
Capellari, Sabina;
Salvi, Fabrizio;
Liguori, Rocco;
Parchi, Piero;
BoReALS;
Bartolomei, Ilaria;
Plasmati, Rosaria;
Pastorelli, Francesca;
Quarta, Cecilia Celidea;
Reale, Vincenzo;
Mariano, Vincenza;
Milletti, David

Publication type:

Article

Diagnostic value of surrogate CSF biomarkers for Creutzfeldt–Jakob disease in the era of RT-QuIC.

Published in:

Journal of Neurology, 2019, v. 266, n. 12, p. 3136, doi. 10.1007/s00415-019-09537-0

By:

Abu-Rumeileh, Samir;
Baiardi, Simone;
Polischi, Barbara;
Mammana, Angela;
Franceschini, Alessia;
Green, Alison;
Capellari, Sabina;
Parchi, Piero

Publication type:

Article

Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.

Published in:

Journal of Neurology, 2017, v. 264, n. 7, p. 1426, doi. 10.1007/s00415-017-8540-x

By:

Giannoccaro, Maria;
Bartoletti-Stella, Anna;
Piras, Silvia;
Pession, Annalisa;
De Massis, Patrizia;
Oppi, Federico;
Stanzani-Maserati, Michelangelo;
Pasini, Elena;
Baiardi, Simone;
Avoni, Patrizia;
Parchi, Piero;
Liguori, Rocco;
Capellari, Sabina

Publication type:

Article

Erratum to: R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease.

Published in:

2013

By:

Vita, Maria Gabriella;
Gaudino, Simona;
Di Giuda, Daniela;
Sauchelli, Donato;
Alboini, Paolo Emilio;
Gangemi, Emma;
Bizzarro, Alessandra;
Scaricamazza, Eugenia;
Capellari, Sabina;
Parchi, Piero;
Masullo, Carlo

Publication type:

Correction Notice

R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease.

Published in:

2013

By:

Vita, Maria;
Gaudino, Simona;
Giuda, Daniela;
Sauchelli, Donato;
Alboini, Paolo;
Gangemi, Emma;
Bizzarro, Alessandra;
Scaricamazza, Eugenia;
Capellari, Sabina;
Parchi, Piero;
Masullo, Carlo

Publication type:

Letter

A case of fatal familial insomnia in Africa.

Published in:

2009

By:

Baldin, Elisa;
Capellari, Sabina;
Provini, Federica;
Corrado, Patrizia;
Liguori, Rocco;
Parchi, Piero;
Montagna, Pasquale;
Cortelli, Pietro

Publication type:

Letter

Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy.

Published in:

Neuroepidemiology, 2020, v. 54, n. 1, p. 83, doi. 10.1159/000503234

By:

Puopolo, Maria;
Catelan, Dolores;
Capellari, Sabina;
Ladogana, Anna;
Sanguedolce, Antonio;
Fedele, Alberto;
Aprile, Valerio;
Turco, Giuseppa Lucia;
Colaizzo, Elisa;
Tiple, Dorina;
Vaianella, Luana;
Parchi, Piero;
Biggeri, Annibale;
Pocchiari, Maurizio

Publication type:

Article

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

Published in:

Acta Neuropathologica Communications, 2018, v. 6, p. 1, doi. 10.1186/s40478-018-0516-2

By:

Race, Brent;
Williams, Katie;
Hughson, Andrew G.;
Jansen, Casper;
Parchi, Piero;
Rozemuller, Annemieke J. M.;
Chesebro, Bruce

Publication type:

Article