AIUTI, ALESSANDRO
AIUTI, ALESSANDRO
Dipartimento di Medicina dei sistemi
. Early-onset monocyte-B-natural killer-dendritic cells’ deficiency successfully treated with hematopoietic stem cell transaplantation
2011-08-01 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
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function
2019-01-01 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
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis
2017-04-01 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
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis
2017-04-01 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
ADA-deficient SCID is associated with a specific microenvironment and bone phenotype characterized by RANKL/OPG imbalance and osteoblast insufficiency
2009-01-01 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
Alterations in the adenosine metabolism and CD39/CD73 adenosinergic machinery cause loss of Treg cell function and autoimmunity in ADA-deficient SCID
2012-02-09 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
Autoantibodies against type I IFNs in patients with life-threatening COVID-19
2020-01-01 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
Autoimmune dysregulation and purine metabolism in adenosine deaminase deficiency
2012-01-01 Sauer, A; Brigida, I; Carriglio, N; Aiuti, A
Autoimmunity and regulatory T cells in 22q11.2 deletion syndrome patients
2015-01-01 DI CESARE, S; Puliafito, P; Ariganello, P; Marcovecchio, Ge; Mandolesi, M; Capolino, R; Digilio, M; Aiuti, A; Rossi, P; Cancrini, C
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
2003-01-01 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
Biological and functional characterization of bone marrow-derived mesenchymal stromal cells from patients affected by primary immunodeficiency
2017-01-01 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
Challenges in vector and trial design using retroviral vectors for long-term gene correction in hematopoietic stem cell gene therapy
2012-06-01 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
Chronic Granulomatous Disease Presenting with Salmonella Brain Abscesses.
2014-01-01 Finocchi, A; Claps, A; Serafinelli, J; Salfa, I; Longo, D; DI MATTEO, G; Aiuti, A; Rossi, P
Clinical features and follow-up in patients with 22q11.2 deletion syndrome
2014-06-01 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
Clinical features and follow-up in patients with 22q11.2 deletion syndrome
2014-01-01 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
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity
2021-01-01 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
Comprehensive genomic access to vector integration in clinical gene therapy.
2009-01-01 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
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity
2020-11-01 Cirillo, E; Giardino, G; Ricci, S; Moschese, V; Lougaris, V; Conti, F; Azzari, C; Barzaghi, F; Canessa, C; Martire, B; Badolato, R; Dotta, L; Soresina, A; Cancrini, C; Finocchi, A; Montin, D; Romano, R; Amodio, D; Ferrua, F; Tommasini, A; Baselli, La; Dellepiane, Rm; Polizzi, A; Chessa, L; Marzollo, A; Cicalese, Mp; Putti, Mc; Pession, A; Aiuti, A; Locatelli, F; Plebani, A; Pignata, C
Defective B cell tolerance in adenosine deaminase deficiency is corrected by gene therapy
2012-06-01 Sauer, A; Morbach, H; Brigida, I; Ng, Y; Aiuti, A; Meffre, E
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease
2014-08-29 Cotugno, N; Finocchi, A; Cagigi, A; DI MATTEO, G; Chiriaco, M; DI CESARE, S; Rossi, P; Aiuti, A; Palma, P; Douagi, I
| 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 | |
| 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-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 | |
| 1-nov-2020 | Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity | Cirillo, E; Giardino, G; Ricci, S; Moschese, V; Lougaris, V; Conti, F; Azzari, C; Barzaghi, F; Canessa, C; Martire, B; Badolato, R; Dotta, L; Soresina, A; Cancrini, C; Finocchi, A; Montin, D; Romano, R; Amodio, D; Ferrua, F; Tommasini, A; Baselli, La; Dellepiane, Rm; Polizzi, A; Chessa, L; Marzollo, A; Cicalese, Mp; Putti, Mc; Pession, A; Aiuti, A; Locatelli, F; Plebani, A; Pignata, C | Articolo su rivista | |
| 1-giu-2012 | Defective B cell tolerance in adenosine deaminase deficiency is corrected by gene therapy | Sauer, A; Morbach, H; Brigida, I; Ng, Y; Aiuti, A; Meffre, E | Articolo su rivista | |
| 29-ago-2014 | Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease | Cotugno, N; Finocchi, A; Cagigi, A; DI MATTEO, G; Chiriaco, M; DI CESARE, S; Rossi, P; Aiuti, A; Palma, P; Douagi, I | Articolo su rivista |