Petersen RB - Search Results

1

Parchi P, Capellari S, Chen SG, Petersen RB, Gambetti P, Kopp N, Brown P, Kitamoto T, Tateishi J, Giese A, Kretzschmar H. Parchi P, et al. Among authors: petersen rb. Nature. 1997 Mar 20;386(6622):232-4. doi: 10.1038/386232a0. Nature. 1997. PMID: 9069279 No abstract available.

2

Regional distribution of protease-resistant prion protein in fatal familial insomnia.

Parchi P, Castellani R, Cortelli P, Montagna P, Chen SG, Petersen RB, Manetto V, Vnencak-Jones CL, McLean MJ, Sheller JR, et al. Parchi P, et al. Among authors: petersen rb. Ann Neurol. 1995 Jul;38(1):21-9. doi: 10.1002/ana.410380107. Ann Neurol. 1995. PMID: 7611720

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: petersen rb. 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: petersen rb. 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

A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene).

Petersen RB, Goldfarb LG, Tabaton M, Brown P, Monari L, Cortelli P, Montagna P, Autilio-Gambetti L, Gajdusek DC, Lugaresi E, et al. Petersen RB, et al. Mol Neurobiol. 1994 Apr-Jun;8(2-3):99-103. doi: 10.1007/BF02780659. Mol Neurobiol. 1994. PMID: 7999319 Review.

6

Fatal familial insomnia and the widening spectrum of prion diseases.

Gambetti P, Petersen R, Monari L, Tabaton M, Autilio-Gambetti L, Cortelli P, Montagna P, Lugaresi E. Gambetti P, et al. Br Med Bull. 1993 Oct;49(4):980-94. doi: 10.1093/oxfordjournals.bmb.a072657. Br Med Bull. 1993. PMID: 8137139 Review. No abstract available.

7

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. 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.

8

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. Among authors: petersen rb. Ann Neurol. 1996 Jun;39(6):767-78. doi: 10.1002/ana.410390613. Ann Neurol. 1996. PMID: 8651649

9

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: petersen rb. Neurology. 1997 Jul;49(1):133-41. doi: 10.1212/wnl.49.1.133. Neurology. 1997. PMID: 9222181

10

Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.

Raymond GJ, Hope J, Kocisko DA, Priola SA, Raymond LD, Bossers A, Ironside J, Will RG, Chen SG, Petersen RB, Gambetti P, Rubenstein R, Smits MA, Lansbury PT Jr, Caughey B. Raymond GJ, et al. Among authors: petersen rb. Nature. 1997 Jul 17;388(6639):285-8. doi: 10.1038/40876. Nature. 1997. PMID: 9230438

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