Adipose tissue-derived mesenchymal stromal cells for clinical application: An efficient isolation approach

Autor: Lisini, D., Nava, S., Pogliani, S., Avanzini, M.A., Lenta, E., Bedini, G., Mantelli, M., Pecciarini, L., Croce, S., Boncoraglio, G., Maccario, R., Parati, E.A., Frigerio, S.

Publikováno v: In Current Research in Translational Medicine February 2019 67(1):20-27

Preemptive Therapy of EBV-Related Lymphoproliferative Disease after Pediatric Haploidentical Stem Cell Transplantation

Autor: Comoli, P. ^*, Basso, S., Zecca, M., Pagliara, D., Baldanti, F., Bernardo, M.E., Barberi, W., Moretta, A., Labirio, M., Paulli, M., Furione, M., Maccario, R., Locatelli, F.

Publikováno v: In American Journal of Transplantation June 2007 7(6):1648-1655

Adoptive transfer of allogeneic Epstein–Barr virus (EBV)-specific cytotoxic T cells with in vitro antitumor activity boostsLMP2-specific immune response in a patient with EBV-related nasopharyngeal carcinoma

Autor: Comoli, P. ^*, De Palma, R., Siena, S., Nocera, A., Basso, S., Del Galdo, F., Schiavo, R., Carminati, O., Tagliamacco, A., Abbate, G.F., Locatelli, F., Maccario, R., Pedrazzoli, P.

Publikováno v: In Annals of Oncology January 2004 15(1):113-117

Expansion of antileukaemia CTL lines and clones for adoptive cell therapy in paediatric patients given allogeneic haematopoietic stem cell transplantation.

Autor: Montagna, D.¹, Maccario, R.², Locatelli, F.² f.locatelli@smatteo.pv.it

Publikováno v: International Journal of Immunogenetics. Aug2008, Vol. 35 Issue 4/5, p389-393. 5p. 3 Graphs.

Clinical features and follow-up in patients with 22q11.2 deletion syndrome

Autor: Cancrini, C, Puliafito, P, Digilio, M, Soresina, A, Martino, S, Rondelli, R, Consolini, R, Ruga, E, Cardinale, F, Finocchi, A, Romiti, Ml, Martire, B, Bacchetta, R, Albano, V, Carotti, A, Specchia, F, Montin, D, Cirillo, E, Cocchi, G, Trizzino, A, Bossi, G, Milanesi, O, Azzari, C, Corsello, G, Pignata, C, Aiuti, A, Pietrogrande, M, Marino, B, Ugazio, A, Plebani, A, Rossi, P, Pierani, P, Gabrielli, A, Danieli, M, De Mattia, D, Sisto, C, Dammacco, F, Ranieri, G, Pession, A, Ricci, G, Minelli, P, Lougaris, V, Badolato, R, Cattaneo, R, Airò, P, Mura, R, Cossu, F, Del Giacco, S, Manconi, P, Consarino, C, Dello Russo, A, Miniero, R, Anastasio, E, Marino, S, Russo, G, Paganelli, R, Sperlì, D, Carpino, L, Aricò, M, Gambineri, E, Lippi, F, Canessa, C, Maggi, E, Romagnani, S, Matucci, A, Vultaggio, A, Gattorno, M, Castagnola, E, Nigro, G, Presta, G, Civino, A, Buzi, F, Gambaretto, G, Fasoli, S, Salpietro, C, Gallizzi, R, Dellepiane, R, Panisi, C, Fabio, G, Carrabba, M, Roncarolo, M, Biondi, A, Vallinoto, C, Poggi, V, Menna, G, Di Nardo, R, Sottile, R, Marone, G, Spadaro, G, Carli, M, Basso, G, Putti, C, Semenzato, G, Agostini, C, D'Angelo, P, Izzi, G, Bertolini, P, Zecca, M, Marseglia, G, Maccario, R, Felici, L, Favre, C, Vecchi, V, Sacchini, P, Rinaldi, G, Livadiotti, S, Simonetti, A, Stabile, A, Duse, M, Iacobini, M, Quinti, I, Fiorilli, M, Moschese, V, Cecere, F, D'Ambrosio, A, De Zan, G, Strafella, S, Tamaro, P, Rabusin, M, Tommasini, A, Tovo, P, De Carli, M, De Carli, S, Nespoli, L, Marinoni, M, Porcellini, A, Lunardi, C, Patuzzo, G, Boner, A, Degani, D

Objective To investigate the clinical manifestations at diagnosis and during follow-up in patients with 22q11.2 deletion syndrome to better define the natural history of the disease. Study design A retrospective and prospective multicenter study was

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2a6eb20a7a207515fdab3011f08fe2c
http://hdl.handle.net/2108/93887