Giaccone G - Search Results

1

Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances".

Coppola C, Saracino D, Oliva M, Cipriano L, Puoti G, Pappatà S, Di Fede G, Catania M, Ricci M, Cimini S, Giaccone G, Bonavita S, Rossi G. Coppola C, et al. Among authors: giaccone g. Neurol Sci. 2021 May;42(5):2021-2029. doi: 10.1007/s10072-020-04774-y. Epub 2020 Oct 2. Neurol Sci. 2021. PMID: 33006056 Free PMC article.

2

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

3

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

4

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.

5

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

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

7

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. Among authors: giaccone g. Neurology. 2004 Sep 14;63(5):910-2. doi: 10.1212/01.wnl.0000137048.80666.86. Neurology. 2004. PMID: 15365148

8

Familial frontotemporal dementia associated with the novel MAPT mutation T427M.

Giaccone G, Rossi G, Farina L, Marcon G, Di Fede G, Catania M, Morbin M, Sacco L, Bugiani O, Tagliavini F. Giaccone G, et al. J Neurol. 2005 Dec;252(12):1543-5. doi: 10.1007/s00415-005-0879-8. Epub 2005 Jun 6. J Neurol. 2005. PMID: 15940384 No abstract available.

9

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. Among authors: giaccone g. 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

10

Cognitive deficits in familial Alzheimer's disease associated with M239V mutation of presenilin 2.

Giovagnoli AR, Marcon G, Giaccone G, Confaloni AM, Tagliavini F. Giovagnoli AR, et al. Among authors: giaccone g. Dement Geriatr Cogn Disord. 2006;22(3):238-43. doi: 10.1159/000094972. Epub 2006 Aug 10. Dement Geriatr Cogn Disord. 2006. PMID: 16902278

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