Zobrazeno 1 - 10
of 608
pro vyhledávání: '"GHIGGERI GM"'
Autor:
Bruschi, M, Bonanni, A, Petretto, A, Vaglio, A, Pratesi, F, Santucci, L, Migliorini, P, Bertelli, R, Galetti, M, Belletti, S, Cavagna, L, Moroni, G, Franceschini, F, Fredi, M, Pazzola, G, Allegri, L, Sinico, Ra, Pesce, G, Bagnasco, M, Manfredi, A, Ramirez, Ga, Ramoino, P, Bianchini, P, Puppo, F, Pupo, F, Negrini, S, Mattana, F, Emmi, G, Garibotto, G, Santoro, D, Scolari, F, Ravelli, A, Tincani, A, Cravedi, P, Volpi, S, Candiano, G, Ghiggeri, Gm
Objective. Neutrophil extracellular traps (NET) expose modified antigens for autoantibodies in vasculitis. Little is known about levels and removal pathways of NET in systemic lupus erythematosus (SLE), especially in lupus nephritis (LN). We determin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1c972769db9baa0ed4931ae4734e937d
http://hdl.handle.net/10281/230174
http://hdl.handle.net/10281/230174
Autor:
Bruschi, M, Moroni, G, Sinico, Ra, Franceschini, F, Fredi, M, Vaglio, A, Cavagna, L, Petretto, A, Pratesi, F, Migliorini, P, Locatelli, F, Pazzola, G, Pesce, G, Bagnasco, M, Manfredi, A, Ramirez, Ga, Esposito, P, Murdaca, G, Negrini, S, Cipriani, L, Trezzi, B, Emmi, G, Cavazzana, I, Binda, V, D'Alessandro, M, Fenaroli, P, Pisani, I, Garibotto, G, Montecucco, C, Santoro, D, Scolari, F, Volpi, S, Mosca, M, Tincani, A, Candiano, G, Prunotto, M, Verrina, E, Angeletti, A, Ravelli, A, Ghiggeri, Gm.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3728::23bff319c0a1221593f76060c231fc9d
http://hdl.handle.net/11568/1066825
http://hdl.handle.net/11568/1066825
Autor:
Rampoldi L, Lamorte G, Bernascone I, Caridi G, Santon D, Boaretto F, Tardanico R, Dagnino M, Colussi G, Scolari F, Ghiggeri GM, Amoroso A, MAZZA, DAVIDE, CASARI , GIORGIO NEVIO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10495::017a0d76d3041d1133a7aa0c76cf7be8
Autor:
Anglani F, Tosetto E, Torregrossa R, Emma F, Barbano G, Ghiggeri GM, Vezzoli G, Murer L, Ratsh IM, Ottonello G, Amenti A, Landro D, Peruzzi L, Cara M, Citron L, D’Angelo A, Gambaro G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10495::70597c4725c7b85e3dd07292e0aa4292
Autor:
Sanna Cherchi, S, Sampogna, Rv, Papeta, N, Burgess, Ke, Nees, Sn, Perry, Bj, Choi, M, Bodria, M, Liu, Y, Weng, Pl, Lozanovski, Vj, Verbitsky, M, Lugani, F, Sterken, R, Paragas, N, Caridi, G, Carrea, A, Dagnino, M, Materna Kiryluk, A, Santamaria, G, Murtas, C, Ristoska Bojkovska, N, Izzi, C, Kacak, N, Bianco, B, Giberti, S, Gigante, M, Piaggio, G, Gesualdo, L, Kosuljandic Vukic, D, Vukojevic, K, Saraga Babic, M, Saraga, M, Gucev, Z, Allegri, L, Latos Bielenska, A, Casu, D, State, M, Scolari, F, Ravazzolo, Roberto, Kiryluk, K, Al Awqati, Q, D'Agati, Vd, Drummond, Ia, Tasic, V, Lifton, Rp, Ghiggeri, Gm, Gharavi, Ag
Publikováno v:
The New England journal of medicine, vol 369, iss 7
BackgroundCongenital abnormalities of the kidney and the urinary tract are the most common cause of pediatric kidney failure. These disorders are highly heterogeneous, and the etiologic factors are poorly understood.MethodsWe performed genomewide lin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cbd40e690159fac589ca0d19f1b485a
https://escholarship.org/uc/item/2hg4p0g8
https://escholarship.org/uc/item/2hg4p0g8
Autor:
SERI M, SAVINO M, BORDO D, CUSANO R, MELONI I, MALATESTA P, CAPRIA M, PASI A. KOIVISTO PA, BOLOGNESI M, GHIGGERI GM, BALDUINI CL, ZELANTE L, RAVAZZOLO R, RENIERI A, SAVOIA, ANNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cba361edcdc44a81f5d6750fa51b1e56
http://hdl.handle.net/11368/1701499
http://hdl.handle.net/11368/1701499
Autor:
SERI M, CUSANO R, GANGAROSSA S, CARIDI G, BORDO D, LO NIGRO C, GHIGGERI GM, RAVAZZOLO R, SAVINO M, DEL VECCHIO M, D'APOLITO M, ZELANTE LL, SAVOIA A, BALDUINI CL, NORIS P, MAGRINI U, BELLETTI S, HEATH KE, BABCOCK M, GLUCKSMAN MJ, ALIPRANDIS E, BIZZARO N, DESNICK RJ, MARTIGNETTI J.A., IOLASCON, ACHILLE
Publikováno v:
Nature genetics. 26(1)
The autosomal dominant, giant-platelet disorders, May-Hegglin anomaly (MHA; MIM 155100), Fechtner syndrome (FTNS; MIM 153640) and Sebastian syndrome (SBS), share the triad of thrombocytopenia, large platelets and characteristic leukocyte inclusions (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5d414d14d2a630e3c46a84cf235627f7
https://pubmed.ncbi.nlm.nih.gov/10973259
https://pubmed.ncbi.nlm.nih.gov/10973259
