Giaccone G - Search Results

1

Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a GRN Mutation.

Cimini S, Bellini S, Saraceno C, Benussi L, Ghidoni R, Giliani SC, Puoti G, Canafoglia L, Giaccone G, Rossi G. Cimini S, et al. Among authors: giaccone g. Int J Mol Sci. 2022 Nov 9;23(22):13753. doi: 10.3390/ijms232213753. Int J Mol Sci. 2022. PMID: 36430231 Free PMC article.

2

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: giaccone g. Cell. 1994 Nov 18;79(4):695-703. doi: 10.1016/0092-8674(94)90554-1. Cell. 1994. PMID: 7954833

3

Diffuse thalamic degeneration in fatal familial insomnia. A morphometric study.

Macchi G, Rossi G, Abbamondi AL, Giaccone G, Mancia D, Tagliavini F, Bugiani O. Macchi G, et al. Among authors: giaccone g. Brain Res. 1997 Oct 10;771(1):154-8. doi: 10.1016/s0006-8993(97)00902-5. Brain Res. 1997. PMID: 9383019

4

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. Among authors: giaccone g. Neurology. 1998 Mar;50(3):688-92. doi: 10.1212/wnl.50.3.688. Neurology. 1998. PMID: 9521257

5

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: giaccone 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.

6

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

Bugiani O, Murrell JR, Giaccone G, Hasegawa M, Ghigo G, Tabaton M, Morbin M, Primavera A, Carella F, Solaro C, Grisoli M, Savoiardo M, Spillantini MG, Tagliavini F, Goedert M, Ghetti B. Bugiani O, et al. Among authors: giaccone g. J Neuropathol Exp Neurol. 1999 Jun;58(6):667-77. doi: 10.1097/00005072-199906000-00011. J Neuropathol Exp Neurol. 1999. PMID: 10374757

7

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

8

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. 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.

9

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

10

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

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