Rossi G - Search Results

1

A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene.

Rossi G, Giaccone G, Maletta R, Morbin M, Capobianco R, Mangieri M, Giovagnoli AR, Bizzi A, Tomaino C, Perri M, Di Natale M, Tagliavini F, Bugiani O, Bruni AC. Rossi G, et al. Neurology. 2004 Sep 14;63(5):910-2. doi: 10.1212/01.wnl.0000137048.80666.86. Neurology. 2004. PMID: 15365148

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. Among authors: rossi g. Neurology. 1999 Dec 10;53(9):2173-6. doi: 10.1212/wnl.53.9.2173. Neurology. 1999. PMID: 10599800

3

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. Neurology. 2000 Aug 8;55(3):405-10. doi: 10.1212/wnl.55.3.405. Neurology. 2000. PMID: 10932276

4

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: rossi g. Neurology. 2003 Nov 11;61(9):1288-91. doi: 10.1212/01.wnl.0000092017.74772.ca. Neurology. 2003. PMID: 14610142

5

Fatal familial insomnia: genetic, neuropathologic, and biochemical study of a patient from a new Italian kindred.

Rossi G, Macchi G, Porro M, Giaccone G, Bugiani M, Scarpini E, Scarlato G, Molini GE, Sasanelli F, Bugiani O, Tagliavini F. Rossi G, et al. Neurology. 1998 Mar;50(3):688-92. doi: 10.1212/wnl.50.3.688. Neurology. 1998. PMID: 9521257

6

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. Among authors: rossi g. Ann Neurol. 2000 Aug;48(2):269-70. Ann Neurol. 2000. PMID: 10939584 No abstract available.

7

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele.

Tagliavini F, Prelli F, Porro M, Rossi G, Giaccone G, Farlow MR, Dlouhy SR, Ghetti B, Bugiani O, Frangione B. Tagliavini F, et al. Among authors: rossi g. Cell. 1994 Nov 18;79(4):695-703. doi: 10.1016/0092-8674(94)90554-1. Cell. 1994. PMID: 7954833

8

A betaPP peptide carboxyl-terminal to Abeta is neurotoxic.

Marcon G, Giaccone G, Canciani B, Cajola L, Rossi G, De Gioia L, Salmona M, Bugiani O, Tagliavini F. Marcon G, et al. Among authors: rossi g. Am J Pathol. 1999 Apr;154(4):1001-7. doi: 10.1016/s0002-9440(10)65352-7. Am J Pathol. 1999. PMID: 10233838 Free PMC article.

9

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: rossi 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.

10

A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

Tagliavini F, Lievens PM, Tranchant C, Warter JM, Mohr M, Giaccone G, Perini F, Rossi G, Salmona M, Piccardo P, Ghetti B, Beavis RC, Bugiani O, Frangione B, Prelli F. Tagliavini F, et al. Among authors: rossi g. J Biol Chem. 2001 Feb 23;276(8):6009-15. doi: 10.1074/jbc.M007062200. Epub 2000 Nov 21. J Biol Chem. 2001. PMID: 11087738 Free article.

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