Capellari S - Search Results

1

Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.

Lodi R, Parchi P, Tonon C, Manners D, Capellari S, Strammiello R, Rinaldi R, Testa C, Malucelli E, Mostacci B, Rizzo G, Pierangeli G, Cortelli P, Montagna P, Barbiroli B. Lodi R, et al. Among authors: capellari s. Brain. 2009 Oct;132(Pt 10):2669-79. doi: 10.1093/brain/awp210. Epub 2009 Sep 15. Brain. 2009. PMID: 19755520 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

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

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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