Rossi G - Search Results

1

The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman Empire.

Coppola C, Saracino D, Oliva M, Puoti G, Lus G, Le Ber I, Pariente J, Tessitore A, Benussi L, Ghidoni R, Carrara M, Ricci M, Redaelli V, Tiraboschi P, Caroppo P, Giaccone G, Bonavita S, Rossi G. Coppola C, et al. Among authors: rossi g. J Alzheimers Dis. 2020;78(1):387-394. doi: 10.3233/JAD-200924. J Alzheimers Dis. 2020. PMID: 33016921

2

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: rossi 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

3

A new function of microtubule-associated protein tau: involvement in chromosome stability.

Rossi G, Dalprà L, Crosti F, Lissoni S, Sciacca FL, Catania M, Di Fede G, Mangieri M, Giaccone G, Croci D, Tagliavini F. Rossi G, et al. Cell Cycle. 2008 Jun 15;7(12):1788-94. doi: 10.4161/cc.7.12.6012. Epub 2008 Jun 25. Cell Cycle. 2008. PMID: 18583940

4

A novel Italian presenilin 2 gene mutation with prevalent behavioral phenotype.

Marcon G, Di Fede G, Giaccone G, Rossi G, Giovagnoli AR, Maccagnano E, Tagliavini F. Marcon G, et al. Among authors: rossi g. J Alzheimers Dis. 2009;16(3):509-11. doi: 10.3233/JAD-2009-0986. J Alzheimers Dis. 2009. PMID: 19276543

5

Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.

Bugiani O, Giaccone G, Rossi G, Mangieri M, Capobianco R, Morbin M, Mazzoleni G, Cupidi C, Marcon G, Giovagnoli A, Bizzi A, Di Fede G, Puoti G, Carella F, Salmaggi A, Romorini A, Patruno GM, Magoni M, Padovani A, Tagliavini F. Bugiani O, et al. Among authors: rossi g. Arch Neurol. 2010 Aug;67(8):987-95. doi: 10.1001/archneurol.2010.178. Arch Neurol. 2010. PMID: 20697050

6

A novel progranulin mutation causing frontotemporal lobar degeneration with heterogeneous phenotypic expression.

Rossi G, Piccoli E, Benussi L, Caso F, Redaelli V, Magnani G, Binetti G, Ghidoni R, Perani D, Giaccone G, Tagliavini F. Rossi G, et al. J Alzheimers Dis. 2011;23(1):7-12. doi: 10.3233/JAD-2010-101461. J Alzheimers Dis. 2011. PMID: 20930271

7

Variability of the clinical phenotype in an Italian family with dementia associated with an intronic deletion in the GRN gene.

Marcon G, Rossi G, Giaccone G, Giovagnoli AR, Piccoli E, Zanini S, Geatti O, Toso V, Grisoli M, Tagliavini F. Marcon G, et al. Among authors: rossi g. J Alzheimers Dis. 2011;26(3):583-90. doi: 10.3233/JAD-2011-110332. J Alzheimers Dis. 2011. PMID: 21677378

8

A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration.

Coppola C, Rossi G, Barbarulo AM, Di Fede G, Foglia C, Piccoli E, Piscosquito G, Saracino D, Tagliavini F, Cotrufo R. Coppola C, et al. Among authors: rossi g. Neurol Sci. 2012 Feb;33(1):93-7. doi: 10.1007/s10072-011-0655-8. Epub 2011 Jun 22. Neurol Sci. 2012. PMID: 21695656

9

New mutations in MAPT gene causing frontotemporal lobar degeneration: biochemical and structural characterization.

Rossi G, Bastone A, Piccoli E, Mazzoleni G, Morbin M, Uggetti A, Giaccone G, Sperber S, Beeg M, Salmona M, Tagliavini F. Rossi G, et al. Neurobiol Aging. 2012 Apr;33(4):834.e1-6. doi: 10.1016/j.neurobiolaging.2011.08.008. Epub 2011 Sep 22. Neurobiol Aging. 2012. PMID: 21943955

10

Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study.

Ghidoni R, Stoppani E, Rossi G, Piccoli E, Albertini V, Paterlini A, Glionna M, Pegoiani E, Agnati LF, Fenoglio C, Scarpini E, Galimberti D, Morbin M, Tagliavini F, Binetti G, Benussi L. Ghidoni R, et al. Among authors: rossi g. Neurodegener Dis. 2012;9(3):121-7. doi: 10.1159/000333132. Epub 2011 Nov 26. Neurodegener Dis. 2012. PMID: 22123177

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