Parchi P - Search Results

1

Variable Protease-Sensitive Prionopathy Transmission to Bank Voles.

Nonno R, Notari S, Di Bari MA, Cali I, Pirisinu L, d'Agostino C, Cracco L, Kofskey D, Vanni I, Lavrich J, Parchi P, Agrimi U, Gambetti P. Nonno R, et al. Among authors: parchi p. Emerg Infect Dis. 2019 Jan;25(1):73-81. doi: 10.3201/eid2501.180807. Emerg Infect Dis. 2019. PMID: 30561322 Free PMC article.

2

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.

3

Truncated forms of the human prion protein in normal brain and in prion diseases.

Chen SG, Teplow DB, Parchi P, Teller JK, Gambetti P, Autilio-Gambetti L. Chen SG, et al. Among authors: parchi p. J Biol Chem. 1995 Aug 11;270(32):19173-80. doi: 10.1074/jbc.270.32.19173. J Biol Chem. 1995. PMID: 7642585 Free article.

4

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.

5

Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein.

Petersen RB, Parchi P, Richardson SL, Urig CB, Gambetti P. Petersen RB, et al. Among authors: parchi p. J Biol Chem. 1996 May 24;271(21):12661-8. doi: 10.1074/jbc.271.21.12661. J Biol Chem. 1996. PMID: 8647879 Free article.

6

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

7

Biopsy diagnosis of Creutzfeldt-Jakob disease by western blot: a case report.

Castellani RJ, Parchi P, Madoff L, Gambetti P, McKeever P. Castellani RJ, et al. Among authors: parchi p. Hum Pathol. 1997 May;28(5):623-6. doi: 10.1016/s0046-8177(97)90086-1. Hum Pathol. 1997. PMID: 9158712

8

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.

9

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.

10

Insomnia in prion diseases: sporadic and familial.

Gambetti P, Parchi P. Gambetti P, et al. Among authors: parchi p. N Engl J Med. 1999 May 27;340(21):1675-7. doi: 10.1056/NEJM199905273402111. N Engl J Med. 1999. PMID: 10341282 No abstract available.

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