Parchi P - Search Results

1

A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.

Jansen C, Parchi P, Capellari S, Strammiello R, Dopper EG, van Swieten JC, Kamphorst W, Rozemuller AJ. Jansen C, et al. Among authors: parchi p. J Neuropathol Exp Neurol. 2011 Aug;70(8):698-702. doi: 10.1097/NEN.0b013e3182270c54. J Neuropathol Exp Neurol. 2011. PMID: 21760536

2

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

3

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

4

Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

Capellari S, Vital C, Parchi P, Petersen RB, Ferrer X, Jarnier D, Pegoraro E, Gambetti P, Julien J. Capellari S, et al. Among authors: parchi p. Neurology. 1997 Jul;49(1):133-41. doi: 10.1212/wnl.49.1.133. Neurology. 1997. PMID: 9222181

5

Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits.

Vital C, Gray F, Vital A, Parchi P, Capellari S, Petersen RB, Ferrer X, Jarnier D, Julien J, Gambetti P. Vital C, et al. Among authors: parchi p. Neuropathol Appl Neurobiol. 1998 Apr;24(2):125-30. doi: 10.1046/j.1365-2990.1998.00098.x. Neuropathol Appl Neurobiol. 1998. PMID: 9634208 Review.

6

Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease.

Parchi P, Chen SG, Brown P, Zou W, Capellari S, Budka H, Hainfellner J, Reyes PF, Golden GT, Hauw JJ, Gajdusek DC, Gambetti P. Parchi P, et al. Proc Natl Acad Sci U S A. 1998 Jul 7;95(14):8322-7. doi: 10.1073/pnas.95.14.8322. Proc Natl Acad Sci U S A. 1998. PMID: 9653185 Free PMC article.

7

Molecular pathology of fatal familial insomnia.

Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P. Parchi P, et al. Brain Pathol. 1998 Jul;8(3):539-48. doi: 10.1111/j.1750-3639.1998.tb00176.x. Brain Pathol. 1998. PMID: 9669705 Free PMC article. Review.

8

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

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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