Capellari S - Search Results

1

Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels.

Lattanzio F, Abu-Rumeileh S, Franceschini A, Kai H, Amore G, Poggiolini I, Rossi M, Baiardi S, McGuire L, Ladogana A, Pocchiari M, Green A, Capellari S, Parchi P. Lattanzio F, et al. Among authors: capellari s. Acta Neuropathol. 2017 Apr;133(4):559-578. doi: 10.1007/s00401-017-1683-0. Epub 2017 Feb 15. Acta Neuropathol. 2017. PMID: 28205010 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

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

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.

5

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

6

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

7

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.

8

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.

9

Creutzfeldt-Jakob disease after receipt of a previously unimplicated brand of dura mater graft.

Hannah EL, Belay ED, Gambetti P, Krause G, Parchi P, Capellari S, Hoffman RE, Schonberger LB. Hannah EL, et al. Among authors: capellari s. Neurology. 2001 Apr 24;56(8):1080-3. doi: 10.1212/wnl.56.8.1080. Neurology. 2001. PMID: 11320182

10

Creutzfeldt-Jakob disease in unusually young patients who consumed venison.

Belay ED, Gambetti P, Schonberger LB, Parchi P, Lyon DR, Capellari S, McQuiston JH, Bradley K, Dowdle G, Crutcher JM, Nichols CR. Belay ED, et al. Among authors: capellari s. Arch Neurol. 2001 Oct;58(10):1673-8. doi: 10.1001/archneur.58.10.1673. Arch Neurol. 2001. PMID: 11594928

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