Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

18 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Variations of the perforin gene in patients with type 1 diabetes.
Orilieri E, Cappellano G, Clementi R, Cometa A, Ferretti M, Cerutti E, Cadario F, Martinetti M, Larizza D, Calcaterra V, D'Annunzio G, Lorini R, Cerutti F, Bruno G, Chiocchetti A, Dianzani U. Orilieri E, et al. Diabetes. 2008 Apr;57(4):1078-83. doi: 10.2337/db07-0947. Epub 2008 Jan 15. Diabetes. 2008. PMID: 18198357 Free article.
Variations of the perforin gene in patients with multiple sclerosis.
Cappellano G, Orilieri E, Comi C, Chiocchetti A, Bocca S, Boggio E, Bernardone IS, Cometa A, Clementi R, Barizzone N, D'Alfonso S, Corrado L, Galimberti D, Scarpini E, Guerini FR, Caputo D, Paolicelli D, Trojano M, Figà-Talamanca L, Salvetti M, Perla F, Leone M, Monaco F, Dianzani U. Cappellano G, et al. Among authors: orilieri e. Genes Immun. 2008 Jul;9(5):438-44. doi: 10.1038/gene.2008.35. Epub 2008 May 22. Genes Immun. 2008. PMID: 18496551
The osteopontin gene +1239A/C single nucleotide polymorphism is associated with type 1 diabetes mellitus in the Italian population.
Chiocchetti A, Orilieri E, Cappellano G, Barizzone N, D' Alfonso S, D' Annunzio G, Lorini R, Ravazzolo R, Cadario F, Martinetti M, Calcaterra V, Cerutti F, Bruno G, Larizza D, Dianzani U. Chiocchetti A, et al. Among authors: orilieri e. Int J Immunopathol Pharmacol. 2010 Jan-Mar;23(1):263-9. doi: 10.1177/039463201002300124. Int J Immunopathol Pharmacol. 2010. PMID: 20378012 Free article.
Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function.
Clementi R, Chiocchetti A, Cappellano G, Cerutti E, Ferretti M, Orilieri E, Dianzani I, Ferrarini M, Bregni M, Danesino C, Bozzi V, Putti MC, Cerutti F, Cometa A, Locatelli F, Maccario R, Ramenghi U, Dianzani U. Clementi R, et al. Among authors: orilieri e. Blood. 2006 Nov 1;108(9):3079-84. doi: 10.1182/blood-2006-02-001412. Epub 2006 May 23. Blood. 2006. PMID: 16720836 Free article.
The 423Q polymorphism of the X-linked inhibitor of apoptosis gene influences monocyte function and is associated with periodic fever.
Ferretti M, Gattorno M, Chiocchetti A, Mesturini R, Orilieri E, Bensi T, Sormani MP, Cappellano G, Cerutti E, Nicola S, Biava A, Bardelli C, Federici S, Ceccherini I, Baldi M, Santoro C, Dianzani I, Martini A, Dianzani U. Ferretti M, et al. Among authors: orilieri e. Arthritis Rheum. 2009 Nov;60(11):3476-84. doi: 10.1002/art.24905. Arthritis Rheum. 2009. PMID: 19877056 Free article.
Association of osteopontin regulatory polymorphisms with systemic sclerosis.
Barizzone N, Marchini M, Cappiello F, Chiocchetti A, Orilieri E, Ferrante D, Corrado L, Mellone S, Scorza R, Dianzani U, D'Alfonso S. Barizzone N, et al. Among authors: orilieri e. Hum Immunol. 2011 Oct;72(10):930-4. doi: 10.1016/j.humimm.2011.06.009. Epub 2011 Jul 1. Hum Immunol. 2011. PMID: 21763380
The impact of osteopontin gene variations on multiple sclerosis development and progression.
Comi C, Cappellano G, Chiocchetti A, Orilieri E, Buttini S, Ghezzi L, Galimberti D, Guerini F, Barizzone N, Perla F, Leone M, D'Alfonso S, Caputo D, Scarpini E, Cantello R, Dianzani U. Comi C, et al. Among authors: orilieri e. Clin Dev Immunol. 2012;2012:212893. doi: 10.1155/2012/212893. Epub 2012 Sep 11. Clin Dev Immunol. 2012. PMID: 23008732 Free PMC article.
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function.
Boggio E, Melensi M, Bocca S, Chiocchetti A, Comi C, Clemente N, Orilieri E, Soluri MF, D'Alfonso S, Mechelli R, Gentile G, Poggi A, Salvetti M, Ramenghi U, Dianzani U. Boggio E, et al. Among authors: orilieri e. Hum Immunol. 2012 May;73(5):585-92. doi: 10.1016/j.humimm.2012.02.025. Epub 2012 Mar 7. Hum Immunol. 2012. PMID: 22425739
18 results