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Human prion diseases.
Parchi P, Gambetti P. Parchi P, et al. Curr Opin Neurol. 1995 Aug;8(4):286-93. doi: 10.1097/00019052-199508000-00007. Curr Opin Neurol. 1995. PMID: 7582044 Review.
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B, et al. Monari L, et al. Proc Natl Acad Sci U S A. 1994 Mar 29;91(7):2839-42. doi: 10.1073/pnas.91.7.2839. Proc Natl Acad Sci U S A. 1994. PMID: 7908444 Free PMC article.
Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion protein.
Cortelli P, Perani D, Parchi P, Grassi F, Montagna P, De Martin M, Castellani R, Tinuper P, Gambetti P, Lugaresi E, Fazio F. Cortelli P, et al. Neurology. 1997 Jul;49(1):126-33. doi: 10.1212/wnl.49.1.126. Neurology. 1997. PMID: 9222180
Fatal familial insomnia in a new Italian kindred.
Padovani A, D'Alessandro M, Parchi P, Cortelli P, Anzola GP, Montagna P, Vignolo LA, Petraroli R, Pocchiari M, Lugaresi E, Gambetti P. Padovani A, et al. Neurology. 1998 Nov;51(5):1491-4. doi: 10.1212/wnl.51.5.1491. Neurology. 1998. PMID: 9818894
A subtype of sporadic prion disease mimicking fatal familial insomnia.
Parchi P, Capellari S, Chin S, Schwarz HB, Schecter NP, Butts JD, Hudkins P, Burns DK, Powers JM, Gambetti P. Parchi P, et al. Neurology. 1999 Jun 10;52(9):1757-63. doi: 10.1212/wnl.52.9.1757. Neurology. 1999. PMID: 10371520
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar H. Parchi P, et al. Ann Neurol. 1999 Aug;46(2):224-33. Ann Neurol. 1999. PMID: 10443888
Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.
Parchi P, Capellari S, Gambetti P. Parchi P, et al. Microsc Res Tech. 2000 Jul 1;50(1):16-25. doi: 10.1002/1097-0029(20000701)50:1<16::AID-JEMT4>3.0.CO;2-Y. Microsc Res Tech. 2000. PMID: 10871544 Review.
A French cluster of Creutzfeldt-Jakob disease: a molecular analysis.
Beaudry P, Parchi P, Peoc'h K, Desbordes P, Dartigues JF, Vital A, Vital C, Capellari S, Gambetti P, Delasnerie-LauprĂȘtre N, Mary JY, Laplanche JL. Beaudry P, et al. Eur J Neurol. 2002 Sep;9(5):457-62. doi: 10.1046/j.1468-1331.2002.00456.x. Eur J Neurol. 2002. PMID: 12220376
Sporadic and familial CJD: classification and characterisation.
Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Gambetti P, et al. Br Med Bull. 2003;66:213-39. doi: 10.1093/bmb/66.1.213. Br Med Bull. 2003. PMID: 14522861 Review.
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