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Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum.
Vicente-Pascual M, Rossi M, Gámez J, Lladó A, Valls J, Grau-Rivera O, Ávila Polo R, Llorens F, Zerr I, Ferrer I, Nos C, Parchi P, Sánchez-Valle R, Gelpí E. Vicente-Pascual M, et al. Among authors: parchi p. Ann Clin Transl Neurol. 2018 Sep 21;5(10):1297-1302. doi: 10.1002/acn3.632. eCollection 2018 Oct. Ann Clin Transl Neurol. 2018. PMID: 30349865 Free PMC article.
Mixed brain pathologies in dementia: the BrainNet Europe consortium experience.
Kovacs GG, Alafuzoff I, Al-Sarraj S, Arzberger T, Bogdanovic N, Capellari S, Ferrer I, Gelpi E, Kövari V, Kretzschmar H, Nagy Z, Parchi P, Seilhean D, Soininen H, Troakes C, Budka H. Kovacs GG, et al. Among authors: parchi p. Dement Geriatr Cogn Disord. 2008;26(4):343-50. doi: 10.1159/000161560. Epub 2008 Oct 10. Dement Geriatr Cogn Disord. 2008. PMID: 18849605 Free article.
Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease.
Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, Heinemann U, Zerr I, Knight RS, Mitrova E, van Duijn C, Budka H. Kovacs GG, et al. Among authors: parchi p. Alzheimer Dis Assoc Disord. 2010 Jan-Mar;24(1):104-7. doi: 10.1097/WAD.0b013e3181ad378c. Alzheimer Dis Assoc Disord. 2010. PMID: 19571726
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.
Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, Shimoji M, Langeveld JP, Castellani R, Notari S, Crain B, Schmidt RE, Geschwind M, Dearmond SJ, Cairns NJ, Dickson D, Honig L, Torres JM, Mastrianni J, Capellari S, Giaccone G, Belay ED, Schonberger LB, Cohen M, Perry G, Kong Q, Parchi P, Tagliavini F, Gambetti P. Zou WQ, et al. Among authors: parchi p. Ann Neurol. 2010 Aug;68(2):162-72. doi: 10.1002/ana.22094. Ann Neurol. 2010. PMID: 20695009 Free PMC article.
Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international study.
McGuire LI, Poleggi A, Poggiolini I, Suardi S, Grznarova K, Shi S, de Vil B, Sarros S, Satoh K, Cheng K, Cramm M, Fairfoul G, Schmitz M, Zerr I, Cras P, Equestre M, Tagliavini F, Atarashi R, Knox D, Collins S, Haïk S, Parchi P, Pocchiari M, Green A. McGuire LI, et al. Among authors: parchi p. Ann Neurol. 2016 Jul;80(1):160-5. doi: 10.1002/ana.24679. Epub 2016 Jun 1. Ann Neurol. 2016. PMID: 27130376 Free PMC article.
Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.
Rossi M, Saverioni D, Di Bari M, Baiardi S, Lemstra AW, Pirisinu L, Capellari S, Rozemuller A, Nonno R, Parchi P. Rossi M, et al. Among authors: parchi p. Acta Neuropathol Commun. 2017 Nov 23;5(1):87. doi: 10.1186/s40478-017-0496-7. Acta Neuropathol Commun. 2017. PMID: 29169405 Free PMC article.
Sporadic Creutzfeldt-Jakob disease.
Zerr I, Parchi P. Zerr I, et al. Among authors: parchi p. Handb Clin Neurol. 2018;153:155-174. doi: 10.1016/B978-0-444-63945-5.00009-X. Handb Clin Neurol. 2018. PMID: 29887134
333 results