Capellari S - Search Results

1

The characterization of AD/PART co-pathology in CJD suggests independent pathogenic mechanisms and no cross-seeding between misfolded Aβ and prion proteins.

Rossi M, Kai H, Baiardi S, Bartoletti-Stella A, Carlà B, Zenesini C, Capellari S, Kitamoto T, Parchi P. Rossi M, et al. Among authors: capellari s. Acta Neuropathol Commun. 2019 Apr 8;7(1):53. doi: 10.1186/s40478-019-0706-6. Acta Neuropathol Commun. 2019. PMID: 30961668 Free PMC article.

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

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.

4

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

5

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.

6

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

7

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

8

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar H. Parchi P, et al. Among authors: capellari s. Ann Neurol. 1999 Aug;46(2):224-33. Ann Neurol. 1999. PMID: 10443888

9

Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease.

Worrall BB, Herman ST, Capellari S, Lynch T, Chin S, Gambetti P, Parchi P. Worrall BB, et al. Among authors: capellari s. J Neurol Neurosurg Psychiatry. 1999 Nov;67(5):671-4. doi: 10.1136/jnnp.67.5.671. J Neurol Neurosurg Psychiatry. 1999. PMID: 10519879 Free PMC article.

10

Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.

Parchi P, Capellari S, Gambetti P. Parchi P, et al. Among authors: capellari s. Microsc Res Tech. 2000 Jul 1;50(1):16-25. doi: 10.1002/1097-0029(20000701)50:1<16::AID-JEMT4>3.0.CO;2-Y. Microsc Res Tech. 2000. PMID: 10871544 Review.

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