AIUTI, ALESSANDRO

AIUTI, ALESSANDRO  

Dipartimento di Medicina dei sistemi  

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Data di pubblicazione Titolo Autore(i) Tipo File
1-ago-2011 . Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation Cancrini, C; Scarselli, A; Scaramuzza, S; Chiriaco, M; Di Cesare, S; DI MATTEO, G; Romiti, Ml; Palma, P; De Felice, L; Palumbo, G; Pinto, R; De Vito, R; Racioppi, L; Livadiotti, S; Fischer, A; Rossi, P; Caniglia, M; Aiuti, A Articolo su rivista
30-apr-2024 A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCID Cesana, D; Cicalese, Mp; Calabria, A; Merli, P; Caruso, R; Volpin, M; Rudilosso, L; Migliavacca, M; Barzaghi, F; Fossati, C; Gazzo, F; Pizzi, S; Ciolfi, A; Bruselles, A; Tucci, F; Spinozzi, G; Pais, G; Benedicenti, F; Barcella, M; Merelli, I; Gallina, P; Giannelli, S; Dionisio, F; Scala, S; Casiraghi, M; Strocchio, L; Vinti, L; Pacillo, L; Draghi, E; Cesana, M; Riccardo, S; Colantuono, C; Six, E; Cavazzana, M; Carlucci, F; Schmidt, M; Cancrini, C; Ciceri, F; Vago, L; Cacchiarelli, D; Gentner, B; Naldini, L; Tartaglia, M; Montini, E; Locatelli, F; Aiuti, A Articolo su rivista
1-nov-2022 A Novel Assay in Whole Blood Demonstrates Restoration of Mitochondrial Activity in Phagocytes After Successful HSCT in Hyperinflamed X-Linked Chronic Granulomatous Disease Migliavacca, M; Basso Ricci, L; Farinelli, G; Calbi, V; Tucci, F; Barzaghi, F; Ferrua, F; Cicalese, Mp; Darin, S; Barzaghi, Lr; Giglio, F; Peccatori, J; Fumagalli, F; Nicoletti, R; Giannelli, S; Sartirana, C; Bandiera, A; Esposito, M; Milani, R; Mazzi, B; Finocchi, A; Marktel, S; Assanelli, A; Locatelli, F; Ciceri, F; Aiuti, A; Bernardo, Me Articolo su rivista
1-gen-2019 A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function Lam, M; Coppola, S; Krumbach, O; Prencipe, G; Insalaco, A; Cifaldi, C; Brigida, I; Zara, E; Scala, S; Di Cesare, S; Martinelli, S; Di Rocco, M; Pascarella, A; Niceta, M; Pantaleoni, F; Ciolfi, A; Netter, P; Carisey, A; Diehl, M; Akbarzadeh, M; Conti, F; Merli, P; Pastore, A; Levi Mortera, S; Camerini, S; Farina, L; Buchholzer, M; Pannone, L; Cao, T; Coban-Akdemir, Z; Jhangiani, S; Muzny, D; Gibbs, R; Basso-Ricci, L; Chiriaco, M; Dvorsky, R; Putignani, L; Carsetti, R; Janning, P; Stray-Pedersen, A; Erichsen, H; Horne, A; Bryceson, Y; Torralba-Raga, L; Ramme, K; Rosti, V; Bracaglia, C; Messia, V; Palma, P; Finocchi, A; Locatelli, F; Chinn, I; Lupski, J; Mace, E; Cancrini, C; Aiuti, A; Ahmadian, M; Orange, J; De Benedetti, F; Tartaglia, M Articolo su rivista
1-apr-2017 A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis Speckmann, C; Doerken, S; Aiuti, A; Albert, Mh; Al-Herz, W; Allende, Lm; Scarselli, A; Avcin, T; Perez-Becker, R; Cancrini, C; Cant, A; Di Cesare, S; Finocchi, A; Fischer, A; Gaspar, Hb; Ghosh, S; Gennery, A; Gilmour, K; González-Granado, Li; Martinez-Gallo, M; Hambleton, S; Hauck, F; Hoenig, M; Moshous, D; Neven, B; Niehues, T; Notarangelo, L; Picard, C; Rieber, N; Schulz, A; Schwarz, K; Seidel, Mg; Soler-Palacin, P; Stepensky, P; Strahm, B; Vraetz, T; Warnatz, K; Winterhalter, C; Worth, A; Fuchs, S; Uhlmann, A; Ehl, S Articolo su rivista
1-apr-2017 A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis Speckmann, C; Doerken, S; Aiuti, A; Albert, Mh; Al-Herz, W; Allende, Lm; Scarselli, A; Avcin, T; Perez-Becker, R; Cancrini, C; Cant, A; Di Cesare, S; Finocchi, A; Fischer, A; Gaspar, Hb; Ghosh, S; Gennery, A; Gilmour, K; González-Granado, Li; Martinez-Gallo, M; Hambleton, S; Hauck, F; Hoenig, M; Moshous, D; Neven, B; Niehues, T; Notarangelo, L; Picard, C; Rieber, N; Schulz, A; Schwarz, K; Seidel, Mg; Soler-Palacin, P; Stepensky, P; Strahm, B; Vraetz, T; Warnatz, K; Winterhalter, C; Worth, A; Fuchs, S; Uhlmann, A; Ehl, S Articolo su rivista
1-ott-2023 Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity Maccari, Me; Wolkewitz, M; Schwab, C; Lorenzini, T; Leiding, Jw; Aladjdi, N; Abolhassani, H; Abou-Chahla, W; Aiuti, A; Azarnoush, S; Baris, S; Barlogis, V; Barzaghi, F; Baumann, U; Bloomfield, M; Bohynikova, N; Bodet, D; Boutboul, D; Bucciol, G; Buckland, Ms; Burns, So; Cancrini, C; Cathébras, P; Cavazzana, M; Cheminant, M; Chinello, M; Ciznar, P; Coulter, Ti; D'Aveni, M; Ekwall, O; Eric, Z; Eren, E; Fasth, A; Frange, P; Fournier, B; Garcia-Prat, M; Gardembas, M; Geier, C; Ghosh, S; Goda, V; Hammarström, L; Hauck, F; Heeg, M; Heropolitanska-Pliszka, E; Hilfanova, A; Jolles, S; Karakoc-Aydiner, E; Kindle, Gr; Kiykim, A; Klemann, C; Koletsi, P; Koltan, S; Kondratenko, I; Körholz, J; Krüger, R; Jeziorski, E; Levy, R; Le Guenno, G; Lefevre, G; Lougaris, V; Marzollo, A; Mahlaoui, N; Malphettes, M; Meinhardt, A; Merlin, E; Meyts, I; Milota, T; Moreira, F; Moshous, D; Mukhina, A; Neth, O; Neubert, J; Neven, B; Nieters, A; Nove-Josserand, R; Oksenhendler, E; Ozen, A; Olbrich, P; Perlat, A; Pac, M; Schmid, Jp; Pacillo, L; Parra-Martinez, A; Paschenko, O; Pellier, I; Sefer, Ap; Plebani, A; Plantaz, D; Prader, S; Raffray, L; Ritterbusch, H; Riviere, Jg; Rivalta, B; Rusch, S; Sakovich, I; Savic, S; Scheible, R; Schleinitz, N; Schuetz, C; Schulz, A; Sediva, A; Semeraro, M; Sharapova, So; Shcherbina, A; Slatter, Ma; Sogkas, G; Soler-Palacin, P; Speckmann, C; Stephan, J; Suarez, F; Tommasini, A; Trück, J; Uhlmann, A; van Aerde, Kj; van Montfrans, J; von Bernuth, H; Warnatz, K; Williams, T; Worth, Ajj; Ip, W; Picard, C; Catherinot, E; Nademi, Z; Grimbacher, B; Forbes Satter, Lr; Kracker, S; Chandra, A; Condliffe, Am; Ehl, S; Seidel, Mg; Seppänen, Mrj; Gennery, A; Kanariou, Mg; Tantou, S; Grigoriadou, S; Cericola, G; Hanitsch, Lg; Scheibenbogen, C; Hlaváčková, Eo; Krivan, G; Mcguire, Fk; Leahy, Tr; Edgar, Jdm; Bakhtiar, S; Bader, P; Rohner, Gb; Haerynck, F; Claes, K; Lehmberg, K; Müller, I; Farmand, S; Fasshauer, M; Graf, D; Neves, Jf; Kostyuchenko, L; Gonzalez-Granado, Li; Jeseňák, M; Carrabba, M; Fabio, G; Pignata, C; Giardino, G; Karadağ, Ik; Yıldıran, A; Hancioglu, G; Králíčková, P; Steinmann, S; Pietrucha, Bm; Gernert, M; Soomann, M; Witte, T; Markocsy, A; Wolska-Kusnierz, B; Randrianomenjanahary, P; Rouger, J; Kostaridou, S; Zabara, Dv; Rodina, Ya; Shvets, Oa Articolo su rivista
1-gen-2009 ADA-deficient SCID is associated with a specific microenvironment and bone phenotype characterized by RANKL/OPG imbalance and osteoblast insufficiency Sauer, A; Mrak, E; Hernandez, R; Zacchi, E; Cavani, F; Casiraghi, M; Grunebaum, E; Roifman, C; Cervi, M; Ambrosi, A; Carlucci, F; Roncarolo, M; Villa, A; Rubinacci, A; Aiuti, A Articolo su rivista
9-feb-2012 Alterations in the adenosine metabolism and CD39/CD73 adenosinergic machinery cause loss of Treg cell function and autoimmunity in ADA-deficient SCID Sauer, A; Brigida, I; Carriglio, N; Hernandez, R; Scaramuzza, S; Clavenna, D; Sanvito, F; Poliani, P; Gagliani, N; Carlucci, F; Tabucchi, A; Roncarolo, M; Traggiai, E; Villa, A; Aiuti, A Articolo su rivista
1-gen-2020 Autoantibodies against type I IFNs in patients with life-threatening COVID-19 Bastard, P; Rosen, Lb; Zhang, Q; Michailidis, E; Hoffmann, H; Zhang, Y; Dorgham, K; Philippot, Q; Rosain, J; Béziat, V; Manry, J; Shaw, E; Haljasmägi, L; Peterson, P; Lorenzo, L; Bizien, L; Trouillet-Assant, S; Dobbs, K; de Jesus, Aa; Belot, A; Kallaste, A; Catherinot, E; Tandjaoui-Lambiotte, Y; Le Pen, J; Kerner, G; Bigio, B; Seeleuthner, Y; Yang, R; Bolze, A; Spaan, An; Delmonte, Om; Abers, Ms; Aiuti, A; Casari, G; Lampasona, V; Piemonti, L; Ciceri, F; Bilguvar, K; Lifton, Rp; Vasse, M; Smadja, Dm; Migaud, M; Hadjadj, J; Terrier, B; Duffy, D; Quintana-Murci, L; van de Beek, D; Roussel, L; Vinh, Dc; Tangye, Sg; Haerynck, F; Dalmau, D; Martinez-Picado, J; Brodin, P; Nussenzweig, Mc; Boisson-Dupuis, S; Rodríguez-Gallego, C; Vogt, G; Mogensen, Th; Oler, Aj; Gu, J; Burbelo, Pd; Cohen, Ji; Biondi, A; Bettini, Lr; D'Angio, M; Bonfanti, P; Rossignol, P; Mayaux, J; Rieux-Laucat, F; Husebye, Es; Fusco, F; Ursini, Mv; Imberti, L; Sottini, A; Paghera, S; Quiros-Roldan, E; Rossi, C; Castagnoli, R; Montagna, D; Licari, A; Marseglia, Gl; Duval, X; Ghosn, J; Tsang, Js; Goldbach-Mansky, R; Kisand, K; Lionakis, Ms; Puel, A; Zhang, S; Holland, Sm; Gorochov, G; Jouanguy, E; Rice, Cm; Cobat, A; Notarangelo, Ld; Abel, L; Su, Hc; Casanova, J Articolo su rivista
1-gen-2012 Autoimmune dysregulation and purine metabolism in adenosine deaminase deficiency Sauer, A; Brigida, I; Carriglio, N; Aiuti, A Articolo su rivista
1-gen-2015 Autoimmunity and regulatory T cells in 22q11.2 deletion syndrome patients DI CESARE, S; Puliafito, P; Ariganello, P; Marcovecchio, Ge; Mandolesi, M; Capolino, R; Digilio, M; Aiuti, A; Rossi, P; Cancrini, C Articolo su rivista
1-gen-2003 Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) Pierdominici, M; Mazzetta, F; Caprini, E; Marziali, M; Digilio, M; Marino, B; Aiuti, A; Amati, F; Russo, G; Novelli, G; Pandolfi, F; Luzi, G; Giovannetti, A Articolo su rivista
1-gen-2017 Biological and functional characterization of bone marrow-derived mesenchymal stromal cells from patients affected by primary immunodeficiency Starc, N; Ingo, D; Conforti, A; Rossella, V; Tomao, L; Pitisci, A; De Mattia, F; Brigida, I; Algeri, M; Montanari, M; Palumbo, G; Merli, P; Rossi, P; Aiuti, A; Locatelli, F; Bernardo, Me Articolo su rivista
1-giu-2012 Challenges in vector and trial design using retroviral vectors for long-term gene correction in hematopoietic stem cell gene therapy Corrigan Curay, J; Cohen Haguenauer, O; O'Reilly, M; Ross, S; Fan, H; Rosenberg, N; Somia, N; King, N; Friedmann, T; Dunbar, C; Aiuti, A; Naldini, L; Baum, C; von Kalle, C; Kiem, H; Montini, E; Bushman, F; Sorrentino, B; Carrondo, M; Malech, H; Gahrton, G; Shapiro, R; Wolff, L; Rosenthal, E; Jambou, R; Zaia, J; Kohn, D Articolo su rivista
1-gen-2014 Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses. Finocchi, A; Claps, A; Serafinelli, J; Salfa, I; Longo, D; DI MATTEO, G; Aiuti, A; Rossi, P Articolo su rivista
1-giu-2014 Clinical features and follow-up in patients with 22q11.2 deletion syndrome 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; Pietrogrande, 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 Articolo su rivista
1-gen-2014 Clinical features and follow-up in patients with 22q11.2 deletion syndrome 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 Articolo su rivista
1-gen-2021 Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity Milito, C; Lougaris, V; Giardino, G; Punziano, A; Vultaggio, A; Carrabba, M; Cinetto, F; Scarpa, R; Delle Piane, R; Baselli, L; Ricci, S; Rivalta, B; Conti, F; Marasco, C; Marzollo, A; Firinu, D; Pulvirenti, F; Lagnese, G; Vivarelli, E; Cancrini, C; Martire, B; Danieli, M; Pession, A; Vacca, A; Azzari, C; Fabio, G; Matucci, A; Soresina, A; Agostini, C; Spadaro, G; Badolato, R; Cicalese, M; Aiuti, A; Plebani, A; Pignata, C; Quinti I., J2j; 9(7):2904-2906. e2. doi: 10. 1016/j. jaip. 2021. 04. 017., E2a Articolo su rivista
1-gen-2009 Comprehensive genomic access to vector integration in clinical gene therapy. Gabriel, R; Eckenberg, R; Paruzynski, A; Bartholomae, C; Nowrouzi, A; Arens, A; Howe, S; Recchia, A; Cattoglio, C; Wang, W; Faber, K; Schwarzwaelder, K; Kirsten, R; Deichmann, A; Ball, C; Balaggan, K; Yanez Munoz, R; Ali, R; Gaspar, H; Biasco, L; Aiuti, A; Cesana, D; Montini, E; Naldini, L; Cohen Hagenauer, O; Mavilio, F; Thrasher, A; Glimm, H; von Kalle, C; Saurin, W; Schmidt, M Articolo su rivista