Capellari S - Search Results

1

Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum.

Bartoletti-Stella A, Vacchiano V, De Pasqua S, Mengozzi G, De Biase D, Bartolomei I, Avoni P, Rizzo G, Parchi P, Donadio V, Chiò A, Pession A, Oppi F, Salvi F, Liguori R, Capellari S; BoReALS. Bartoletti-Stella A, et al. Among authors: capellari s. J Neurol. 2021 Oct;268(10):3766-3776. doi: 10.1007/s00415-021-10521-w. Epub 2021 Mar 26. J Neurol. 2021. PMID: 33770234 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

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

4

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

5

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.

6

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

7

Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene.

Capellari S, Parchi P, Wolff BD, Campbell J, Atkinson R, Posey DM, Petersen RB, Gambetti P. Capellari S, et al. Neurology. 2002 Nov 26;59(10):1628-30. doi: 10.1212/01.wnl.0000035533.86833.28. Neurology. 2002. PMID: 12451210

8

Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.

Notari S, Capellari S, Giese A, Westner I, Baruzzi A, Ghetti B, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. Among authors: capellari s. J Biol Chem. 2004 Apr 16;279(16):16797-804. doi: 10.1074/jbc.M313220200. Epub 2004 Jan 29. J Biol Chem. 2004. PMID: 14754888 Free article.

9

Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene.

Capellari S, Cardone F, Notari S, Schininà ME, Maras B, Sità D, Baruzzi A, Pocchiari M, Parchi P. Capellari S, et al. Neurology. 2005 Mar 8;64(5):905-7. doi: 10.1212/01.WNL.0000152837.82388.DE. Neurology. 2005. PMID: 15753435

10

A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule.

Notari S, Capellari S, Langeveld J, Giese A, Strammiello R, Gambetti P, Kretzschmar HA, Parchi P. Notari S, et al. Among authors: capellari s. Lab Invest. 2007 Nov;87(11):1103-12. doi: 10.1038/labinvest.3700676. Epub 2007 Sep 24. Lab Invest. 2007. PMID: 17893675 Free article.

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