Parchi P - Search Results

1

α-Synuclein RT-QuIC assay in cerebrospinal fluid of patients with dementia with Lewy bodies.

Bongianni M, Ladogana A, Capaldi S, Klotz S, Baiardi S, Cagnin A, Perra D, Fiorini M, Poleggi A, Legname G, Cattaruzza T, Janes F, Tabaton M, Ghetti B, Monaco S, Kovacs GG, Parchi P, Pocchiari M, Zanusso G. Bongianni M, et al. Among authors: parchi p. Ann Clin Transl Neurol. 2019 Oct;6(10):2120-2126. doi: 10.1002/acn3.50897. Epub 2019 Oct 10. Ann Clin Transl Neurol. 2019. PMID: 31599499 Free PMC article.

2

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.

Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, Petersen RB, Gambetti P. Parchi P, et al. Ann Neurol. 1996 Jun;39(6):767-78. doi: 10.1002/ana.410390613. Ann Neurol. 1996. PMID: 8651649

3

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. Among authors: parchi p. Neurology. 1998 Nov;51(5):1491-4. doi: 10.1212/wnl.51.5.1491. Neurology. 1998. PMID: 9818894

4

A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.

Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H. Hainfellner JA, et al. Among authors: parchi p. Ann Neurol. 1999 Jun;45(6):812-6. Ann Neurol. 1999. PMID: 10360778

5

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

6

Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.

Notari S, Capellari S, Giese A, Westner I, Baruzzi A, Ghetti B, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. Among authors: parchi p. J Biol Chem. 2004 Apr 16;279(16):16797-804. doi: 10.1074/jbc.M313220200. Epub 2004 Jan 29. J Biol Chem. 2004. PMID: 14754888 Free article.

7

Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease.

Castellani RJ, Colucci M, Xie Z, Zou W, Li C, Parchi P, Capellari S, Pastore M, Rahbar MH, Chen SG, Gambetti P. Castellani RJ, et al. Among authors: parchi p. Neurology. 2004 Aug 10;63(3):436-42. doi: 10.1212/01.wnl.0000135153.96325.3b. Neurology. 2004. PMID: 15304573

8

Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene.

Capellari S, Cardone F, Notari S, Schininà ME, Maras B, Sità D, Baruzzi A, Pocchiari M, Parchi P. Capellari S, et al. Among authors: parchi p. Neurology. 2005 Mar 8;64(5):905-7. doi: 10.1212/01.WNL.0000152837.82388.DE. Neurology. 2005. PMID: 15753435

9

Sporadic fatal insomnia in a fatal familial insomnia pedigree.

Capellari S, Parchi P, Cortelli P, Avoni P, Casadei GP, Bini C, Baruzzi A, Lugaresi E, Pocchiari M, Gambetti P, Montagna P. Capellari S, et al. Among authors: parchi p. Neurology. 2008 Mar 11;70(11):884-5. doi: 10.1212/01.wnl.0000287140.94379.52. Neurology. 2008. PMID: 18332347 No abstract available.

10

Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.

Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J, Ghetti B, Langeveld JP, Zou WQ, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. Among authors: parchi p. J Biol Chem. 2008 Nov 7;283(45):30557-65. doi: 10.1074/jbc.M801877200. Epub 2008 Aug 27. J Biol Chem. 2008. PMID: 18753138 Free PMC article.

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