Capellari S - Search Results

1

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: capellari s. Neurology. 1998 Jul;51(1):271-4. doi: 10.1212/wnl.51.1.271. Neurology. 1998. PMID: 9674819

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

4

Typing prion isoforms.

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: capellari s. Nature. 1997 Mar 20;386(6622):232-4. doi: 10.1038/386232a0. Nature. 1997. PMID: 9069279 No abstract available.

5

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

6

Allelic origin of the abnormal prion protein isoform in familial prion diseases.

Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P. Chen SG, et al. Among authors: capellari s. Nat Med. 1997 Sep;3(9):1009-15. doi: 10.1038/nm0997-1009. Nat Med. 1997. PMID: 9288728

7

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: capellari s. 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.

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. Among authors: capellari s. 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. Among authors: capellari s. 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

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. Among authors: capellari s. Neurology. 1999 Jun 10;52(9):1757-63. doi: 10.1212/wnl.52.9.1757. Neurology. 1999. PMID: 10371520

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