Puoti G - Search Results

1

Sporadic human prion diseases: molecular insights and diagnosis.

Puoti G, Bizzi A, Forloni G, Safar JG, Tagliavini F, Gambetti P. Puoti G, et al. Lancet Neurol. 2012 Jul;11(7):618-28. doi: 10.1016/S1474-4422(12)70063-7. Lancet Neurol. 2012. PMID: 22710755 Review.

2

Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain.

Puoti G, Giaccone G, Rossi G, Canciani B, Bugiani O, Tagliavini F. Puoti G, et al. Neurology. 1999 Dec 10;53(9):2173-6. doi: 10.1212/wnl.53.9.2173. Neurology. 1999. PMID: 10599800

3

Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion protein.

Giaccone G, Canciani B, Puoti G, Rossi G, Goffredo D, Iussich S, Fociani P, Tagliavini F, Bugiani O. Giaccone G, et al. Among authors: puoti g. Brain Pathol. 2000 Jan;10(1):31-7. doi: 10.1111/j.1750-3639.2000.tb00240.x. Brain Pathol. 2000. PMID: 10668893 Free PMC article.

4

Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene.

Rossi G, Giaccone G, Giampaolo L, Iussich S, Puoti G, Frigo M, Cavaletti G, Frattola L, Bugiani O, Tagliavini F. Rossi G, et al. Among authors: puoti g. Neurology. 2000 Aug 8;55(3):405-10. doi: 10.1212/wnl.55.3.405. Neurology. 2000. PMID: 10932276

5

Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation.

Puoti G, Rossi G, Giaccone G, Awan T, Lievens PM, Defanti CA, Tagliavini F, Bugiani O. Puoti G, et al. Ann Neurol. 2000 Aug;48(2):269-70. Ann Neurol. 2000. PMID: 10939584 No abstract available.

6

Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene.

Pietrini V, Puoti G, Limido L, Rossi G, Di Fede G, Giaccone G, Mangieri M, Tedeschi F, Bondavalli A, Mancia D, Bugiani O, Tagliavini F. Pietrini V, et al. Among authors: puoti g. Neurology. 2003 Nov 11;61(9):1288-91. doi: 10.1212/01.wnl.0000092017.74772.ca. Neurology. 2003. PMID: 14610142

7

Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques.

Puoti G, Limido L, Cotrufo R, Di Fede G, Tagliavini F. Puoti G, et al. Neurology. 2004 Apr 13;62(7):1239; author reply 1239. doi: 10.1212/wnl.62.7.1239. Neurology. 2004. PMID: 15079047 No abstract available.

8

Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc.

Puoti G, Giaccone G, Mangieri M, Limido L, Fociani P, Zerbi P, Suardi S, Rossi G, Iussich S, Capobianco R, Di Fede G, Marcon G, Cotrufo R, Filippini G, Bugiani O, Tagliavini F. Puoti G, et al. J Neuropathol Exp Neurol. 2005 Oct;64(10):902-9. doi: 10.1097/01.jnen.0000183346.19447.55. J Neuropathol Exp Neurol. 2005. PMID: 16215462

9

The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.

Di Fede G, Giaccone G, Limido L, Mangieri M, Suardi S, Puoti G, Morbin M, Mazzoleni G, Ghetti B, Tagliavini F. Di Fede G, et al. Among authors: puoti g. J Neuropathol Exp Neurol. 2007 Feb;66(2):124-30. doi: 10.1097/nen.0b013e3180302060. J Neuropathol Exp Neurol. 2007. PMID: 17278997

10

A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings.

Mauro C, Giaccone G, Piscosquito G, Lavorgna A, Nigro M, Di Fede G, Leonardi A, Coppola C, Formisano S, Tagliavini F, Cotrufo R, Puoti G. Mauro C, et al. Among authors: puoti g. J Neurol Neurosurg Psychiatry. 2008 Dec;79(12):1395-8. doi: 10.1136/jnnp.2007.142976. J Neurol Neurosurg Psychiatry. 2008. PMID: 19010951

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