Zobrazeno 1 - 10
of 19
pro vyhledávání: '"D' Alfonso S"'
Autor:
Ceccarelli, F., D Alfonso, S., Carlo Perricone, Carlomagno, Y., Alessandri, C., Croia, C., Barizzone, N., Montecucco, C., Galeazzi, M., Sebastiani, G. D., Minisola, G., Fiocco, U., Valesini, G.
Publikováno v:
Publons
Scopus-Elsevier
Europe PubMed Central
Scopus-Elsevier
Europe PubMed Central
Several single nucleotide polymorphisms (SNPs) have been associated with rheumatoid arthritis (RA) such as peptidylarginine deiminase-4 (PADI4), osteopontin (OPN), and perforin (PRF1) genes. Thus, we aimed at analysing the influence of eight SNPs in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7e8119255a18fe95413225c458e6986f
http://hdl.handle.net/11391/1516381
http://hdl.handle.net/11391/1516381
Autor:
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., Graziella BRUNO, Larizza, D., Dianzani, U.
Publikováno v:
Scopus-Elsevier
Secreted phosphoprotein 1, also known as Osteopontin (Opn), is a proinflammatory cytokine involved in the TH1 response and is highly expressed in the islets and pancreatic lymph nodes of non-obese diabetic mice before the onset of diabetes. In humans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c47242bfc9fefe45877bb11395f9c63
http://hdl.handle.net/11567/223871
http://hdl.handle.net/11567/223871
Autor:
Riz, M., Galimberti, D., Scalabrini, D., Fenoglio, C., CRISTOFORO COMI, Venturelli, E., Cortini, F., Piola, M., Brighina, E., Dianzani, U., D Alfonso, S., Monaco, F., Bresolin, N., Scarpini, E.
Publikováno v:
Publons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0411b180e243935c53dac13f092811da
http://hdl.handle.net/2434/42135
http://hdl.handle.net/2434/42135
Autor:
D Alfonso, S., Lorenza Nisticò, Bocchio, D., Bomprezzi, R., Marrosu, M. G., Murru, M. R., Lai, M., Massacesi, L., Ballerini, C., Repice, A., Salvetti, M., Montesperelli, C., Ristori, G., Trojano, M., Liguori, M., Gambi, D., Quattrone, A., Tosi, R., Momigliano-Richiardi, P.
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Subsequent to a genomic linkage study on Sardinian and Continental Italian families, we considered the possibility that some of the tested microsatellite markers showed association to MS. Markers selected on the basis of the data obtained in the orig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5fa9c02396237218fc2834600591afd3
https://pubmed.ncbi.nlm.nih.gov/10871779
https://pubmed.ncbi.nlm.nih.gov/10871779
Akademický článek
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Autor:
Sciacca, F. L., Ferri, C., D`Alfonso, S., Bolognesi, E., Boneschi, F. M., Cuzzilla, B., Colombo, B., Comi, G., Canal, N., Grimaldi, L. M.
Publikováno v:
Journal of Neuroimmunology; 2000, Vol. 104 Issue: 2 p174-178, 5p
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0d687976550717c941241a9758f8babf
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033303241&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0033303241&partnerID=MN8TOARS
Autor:
Calini, D., Corrado, L., Del Bo, R., Gagliardi, S., Pensato, V., Verde, F., Corti, S., Mazzini, L., Milani, P., Castellotti, B., Bertolin, C., Sorarù, G., Cereda, C., Comi, G. P., D Alfonso, S., Gellera, C., Ticozzi, N., Landers, J. E., Ratti, A., Vincenzo Silani, Slagen, Consortium
Publikováno v:
Scopus-Elsevier
Mutations in the prion-like domain (PrLD) of hnRNPA1 and A2/B1 genes were recently identified in 2 families with inclusion body myopathy associated with Paget disease of bone, frontotemporal dementia (FTD), and amyotrophic lateral sclerosis, and in A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::478e25040d1776ad93b386b77e92eb74
http://www.scopus.com/inward/record.url?eid=2-s2.0-84895605702&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84895605702&partnerID=MN8TOARS
Autor:
Goris, A., Pauwels, I., Gustavsen, M. W., Son, B., Hilven, K., Bos, S. D., Celius, E. G., Berg-Hansen, P., Aarseth, J., Myhr, K. M., D Alfonso, S., Barizzone, N., Leone, M. A., Boneschi, F. M., Sorosina, M., Liberatore, G., Kockum, I., Olsson, T., Hillert, J., Alfredsson, L., Bedri, S. K., Hemmer, B., Buck, D., Berthele, A., Knier, B., Biberacher, V., Pesch, V., Sindic, C., Oturai, A. B., Sondergaard, H. B., Sellebjerg, F., Jensen, P. E., Comabella, M., Montalban, X., Perez-Boza, J., Malhotra, S., Lechner-Scott, J., Broadley, S., Mark Slee, Taylor, B., Kermode, A., Gourraud, P. A., Sawcer, S., Andreassen, B. K., Dubois, B., Harbo, H. F., Int Multiple Sclerosis Genetics, Co
Publikováno v:
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::53da84e878f4884c9e3a3afd9771486e
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000354441300359&KeyUID=WOS:000354441300359
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000354441300359&KeyUID=WOS:000354441300359
Autor:
Cucovici, A., Arcuti, S., Andrei Ivashynka, Vecchio, D., Naldi, P., D Alfonso, S., Copetti, M., Leone, M.
Publikováno v:
Publons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5fff65717a2144fa0f22b53e179ad2d
https://publons.com/publon/10766328/
https://publons.com/publon/10766328/