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165 results
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A Clinical Evidence of a Correlation Between Insulin Resistance and the ALCAT Food Intolerance Test.
Pompei P, Grappasonni I, Scuri S, Petrelli F, Traini E, Sorrentino S, Di Fede G. Pompei P, et al. Among authors: di fede g. Altern Ther Health Med. 2019 Mar;25(2):22-38. Altern Ther Health Med. 2019. PMID: 30990791
Non-Celiac Gluten Sensitivity in patients with severe abdominal pain and bloating: The accuracy of ALCAT 5.
Di Stefano M, Pesatori EV, Manfredi GF, De Amici M, Grandi G, Gabriele A, Iozzi D, Di Fede G. Di Stefano M, et al. Among authors: di fede g. Clin Nutr ESPEN. 2018 Dec;28:127-131. doi: 10.1016/j.clnesp.2018.08.017. Epub 2018 Sep 9. Clin Nutr ESPEN. 2018. PMID: 30390869
Translational Research in Alzheimer's and Prion Diseases.
Di Fede G, Giaccone G, Salmona M, Tagliavini F. Di Fede G, et al. J Alzheimers Dis. 2018;62(3):1247-1259. doi: 10.3233/JAD-170770. J Alzheimers Dis. 2018. PMID: 29172000 Free PMC article. Review.
MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.
Moda F, Suardi S, Di Fede G, Indaco A, Limido L, Vimercati C, Ruggerone M, Campagnani I, Langeveld J, Terruzzi A, Brambilla A, Zerbi P, Fociani P, Bishop MT, Will RG, Manson JC, Giaccone G, Tagliavini F. Moda F, et al. Among authors: di fede g. Brain Pathol. 2012 Sep;22(5):662-9. doi: 10.1111/j.1750-3639.2012.00572.x. Epub 2012 Feb 21. Brain Pathol. 2012. PMID: 22288561
Altered Expression of Circulating Cdc42 in Frontotemporal Lobar Degeneration.
Saraceno C, Catania M, Paterlini A, Fostinelli S, Ciani M, Zanardini R, Binetti G, Di Fede G, Caroppo P, Benussi L, Ghidoni R, Bolognin S. Saraceno C, et al. Among authors: di fede g. J Alzheimers Dis. 2018;61(4):1477-1483. doi: 10.3233/JAD-170722. J Alzheimers Dis. 2018. PMID: 29376863
Molecular subtypes of Alzheimer's disease.
Di Fede G, Catania M, Maderna E, Ghidoni R, Benussi L, Tonoli E, Giaccone G, Moda F, Paterlini A, Campagnani I, Sorrentino S, Colombo L, Kubis A, Bistaffa E, Ghetti B, Tagliavini F. Di Fede G, et al. Sci Rep. 2018 Feb 19;8(1):3269. doi: 10.1038/s41598-018-21641-1. Sci Rep. 2018. PMID: 29459625 Free PMC article.
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
Capobianco R, Casalone C, Suardi S, Mangieri M, Miccolo C, Limido L, Catania M, Rossi G, Di Fede G, Giaccone G, Bruzzone MG, Minati L, Corona C, Acutis P, Gelmetti D, Lombardi G, Groschup MH, Buschmann A, Zanusso G, Monaco S, Caramelli M, Tagliavini F. Capobianco R, et al. Among authors: di fede g. PLoS Pathog. 2007 Mar;3(3):e31. doi: 10.1371/journal.ppat.0030031. PLoS Pathog. 2007. PMID: 17352534 Free PMC article.
Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene.
Di Fede G, Catania M, Atzori C, Moda F, Pasquali C, Indaco A, Grisoli M, Zuffi M, Guaita MC, Testi R, Taraglio S, Sessa M, Gusmaroli G, Spinelli M, Salzano G, Legname G, Tarletti R, Godi L, Pocchiari M, Tagliavini F, Imperiale D, Giaccone G. Di Fede G, et al. Acta Neuropathol Commun. 2019 Jan 3;7(1):1. doi: 10.1186/s40478-018-0656-4. Acta Neuropathol Commun. 2019. PMID: 30606247 Free PMC article.
Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features.
Giaccone G, Morbin M, Moda F, Botta M, Mazzoleni G, Uggetti A, Catania M, Moro ML, Redaelli V, Spagnoli A, Rossi RS, Salmona M, Di Fede G, Tagliavini F. Giaccone G, et al. Among authors: di fede g. Acta Neuropathol. 2010 Dec;120(6):803-12. doi: 10.1007/s00401-010-0747-1. Epub 2010 Sep 15. Acta Neuropathol. 2010. PMID: 20842367
Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family.
Giovagnoli AR, Di Fede G, Aresi A, Reati F, Rossi G, Tagliavini F. Giovagnoli AR, et al. Among authors: di fede g. Neurol Sci. 2008 Dec;29(6):405-10. doi: 10.1007/s10072-008-1025-z. Epub 2008 Nov 21. Neurol Sci. 2008. PMID: 19030774
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