Parchi P - Search Results

1

Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.

Hermann P, Appleby B, Brandel JP, Caughey B, Collins S, Geschwind MD, Green A, Haïk S, Kovacs GG, Ladogana A, Llorens F, Mead S, Nishida N, Pal S, Parchi P, Pocchiari M, Satoh K, Zanusso G, Zerr I. Hermann P, et al. Among authors: parchi p. Lancet Neurol. 2021 Mar;20(3):235-246. doi: 10.1016/S1474-4422(20)30477-4. Lancet Neurol. 2021. PMID: 33609480 Free PMC article. Review.

2

Creutzfeldt-Jakob disease after liver transplantation.

Créange A, Gray F, Cesaro P, Adle-Biassette H, Duvoux C, Cherqui D, Bell J, Parchi P, Gambetti P, Degos JD. Créange A, et al. Among authors: parchi p. Ann Neurol. 1995 Aug;38(2):269-72. doi: 10.1002/ana.410380223. Ann Neurol. 1995. PMID: 7654078

3

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E. Gambetti P, et al. Among authors: parchi p. Brain Pathol. 1995 Jan;5(1):43-51. doi: 10.1111/j.1750-3639.1995.tb00576.x. Brain Pathol. 1995. PMID: 7767490 Review.

4

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. Among authors: parchi p. 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.

5

Early pathologic and biochemical changes in Creutzfeldt-Jakob disease: study of brain biopsies.

Castellani R, Parchi P, Stahl J, Capellari S, Cohen M, Gambetti P. Castellani R, et al. Among authors: parchi p. Neurology. 1996 Jun;46(6):1690-3. doi: 10.1212/wnl.46.6.1690. Neurology. 1996. PMID: 8649571

6

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

7

Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case.

Ghorayeb I, Series C, Parchi P, Sawan B, Guez S, Laplanche JL, Capellari S, Gambetti P, Vital C. Ghorayeb I, et al. Among authors: parchi p. Neurology. 1998 Jul;51(1):271-4. doi: 10.1212/wnl.51.1.271. Neurology. 1998. PMID: 9674819

8

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

9

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

10

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

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