CANCRINI, CATERINA
CANCRINI, CATERINA
Dipartimento di Medicina dei sistemi
(2012). Analysis of B cell immune recovery after hematopoietic stem cell transplantation in primary immunodeficiency.
2012-01-01 Scarselli, ; A, ; Di, C; S, ; Cascioli, ; S, ; Romiti, ; Ml, ; Finocchi, A; Palma, ; P, ; Pinto, ; Rm, ; Palumbo, ; G, ; Aiuti, ; A, ; Carsetti, ; R, ; Cancrini, C
. 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
22q11.2 Deletion and Duplication Syndromes and COVID-19
2022-01-01 Blaine Crowley 1, T; 1, Dmm; E Sullivan 2, K; 2 COVID group report Collaborators, Iq; Cancrini, C; Gennery, A; Kumararatne, D; McDonald McGinn, D; Oskarsdottir, S; Richter, A; E Sullivan, K; Vergaelen, E
[Perinatal infections of B19 Parvoviruses]
2002-05-01 DI DOMENICO, C; Moschese, V; Chini, L; Zirletta, E; Cancrini, C; DI PAOLO, A; A, ; Rossi, P; Scalamandre', A
A 23-Year Follow-Up of a Patient with Gain-of-Function IkB-Alpha Mutation and Stable Full Chimerism After Hematopoietic Stem Cell Transplantation.
2020-07-24 Conti, F; Carsetti, R; Casanova, J; Fischer, A; Cancrini, C
A case of APDS patient: defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment
2017-01-01 Chiriaco, M; Brigida, I; Ariganello, P; DI CESARE, S; DI MATTEO, G; Taus, F; Cittaro, D; Lazarevic, D; Scarselli, A; Santilli, V; Attardi, E; Stupka, E; Giannelli, S; Fraziano, M; Finocchi, A; Rossi, P; Aiuti, A; Palma, P; Cancrini, C
A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCID
2024-04-30 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
A hypermorphic I kappa B alpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency
2003-01-01 Courtois, G; Smahi, A; Reichenbach, J; Doffinger, R; Cancrini, C; Bonnet, M; Puel, A; Chable Bessia, C; Yamaoka, S; Feinberg, J; Dupuis Girod, S; Bodemer, C; Livadiotti, S; Novelli, F; Rossi, P; Fischer, A; Israel, A; Munnich, A; Le Deist, F; Casanova, Jl
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 systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency
2014-04-01 Lee, Y; Frugoni, F; Dobbs, K; Walter, J; Giliani, S; Gennery, A; Al Herz, W; Haddad, E; Ledeist, F; Bleesing, J; Henderson, L; Pai, S; Nelson, R; El Ghoneimy, D; El Feky, R; Reda, S; Hossny, E; Soler Palacin, P; Fuleihan, R; Patel, N; Massaad, M; Geha, R; Puck, J; Palma, P; Cancrini, C; Chen, K; Vihinen, M; Alt, F; Notarangelo, L
Accumulation of peripheral autoreactive B cells in the absence of functional human regulatory T cells
2013-01-01 Kinnunen, T; Chamberlain, N; Morbach, H; Choi, J; Kim, S; Craft, J; Mayer, L; Cancrini, C; Passerini, L; Bacchetta, R; Ochs, H; Torgerson TR and Meffre, E
Activated phosphoinositde 3-kinase (PI3Kδ) syndrome: an Italian point of view on diagnosis and new advances in treatment
2024-05-20 Lougaris, V; Piane, Fl; Cancrini, C; Conti, F; Tommasini, A; Badolato, R; Trizzino, A; Zecca, M; De Rosa, A; Barzaghi, F; Pignata, C
Activated phosphoinositide 3-dinase delta syndrome (APDS): An update
2022-01-01 Lougaris, V; Cancrini, C; Rivalta, B; Castagnoli, R; Giardino, G; Volpi, S; Leonardi, L; La Torre, F; Federici, S; Corrente, S; Cinicola, B; Soresina, A; Marseglia, G; Cardinale, F
Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity
2023-10-01 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
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy
2016-01-01 Cifaldi, C; Scarselli, A; Petricone, D; DI CESARE, S; Chiriaco, M; Claps, A; Rossi, P; Calzoni, E; Yamazaki, Y; Notarangelo, L; DI MATTEO, G; Cancrini, C; Finocchi, A
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia
2021-09-01 Desimio, Mg; Finocchi, A; Di Matteo, G; Di Cesare, S; Giancotta, C; Conti, F; Chessa, L; Piane, M; Montin, D; Dellepiane, M; Rossi, P; Cancrini, C; Doria, M
Analysis of HIV-1 reverse transcriptase gene mutations in infected children treated with zidovudine
1998-01-01 Orlandi, P; Cancrini, C; Scaccia, S; Romiti, Ml; Livadiotti, S; Gattinara, Gc; Angelini, F; Cox, S; Rossi, P
Anti-infective prophylaxis for primary immunodeficiencies: what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature
2013-10-01 Moschese, V; Martire, B; Soresina, A; Chini, L; Graziani, S; Monteferrario, E; Bacchetta, R; Cancrini, C; Fiorilli, M; Gambineri, E; Pession, A; Pignata, C; Quinti, I; Rondelli, R; Rossi, P; Ugazio, A; Plebani, A; Pietrogrande, M
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
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2012 | (2012). Analysis of B cell immune recovery after hematopoietic stem cell transplantation in primary immunodeficiency. | Scarselli, ; A, ; Di, C; S, ; Cascioli, ; S, ; Romiti, ; Ml, ; Finocchi, A; Palma, ; P, ; Pinto, ; Rm, ; Palumbo, ; G, ; Aiuti, ; A, ; Carsetti, ; R, ; Cancrini, C | Articolo su rivista | |
| 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-2022 | 22q11.2 Deletion and Duplication Syndromes and COVID-19 | Blaine Crowley 1, T; 1, Dmm; E Sullivan 2, K; 2 COVID group report Collaborators, Iq; Cancrini, C; Gennery, A; Kumararatne, D; McDonald McGinn, D; Oskarsdottir, S; Richter, A; E Sullivan, K; Vergaelen, E | Articolo su rivista | |
| 1-mag-2002 | [Perinatal infections of B19 Parvoviruses] | DI DOMENICO, C; Moschese, V; Chini, L; Zirletta, E; Cancrini, C; DI PAOLO, A; A, ; Rossi, P; Scalamandre', A | Articolo su rivista | |
| 24-lug-2020 | A 23-Year Follow-Up of a Patient with Gain-of-Function IkB-Alpha Mutation and Stable Full Chimerism After Hematopoietic Stem Cell Transplantation. | Conti, F; Carsetti, R; Casanova, J; Fischer, A; Cancrini, C | Articolo su rivista | |
| 1-gen-2017 | A case of APDS patient: defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment | Chiriaco, M; Brigida, I; Ariganello, P; DI CESARE, S; DI MATTEO, G; Taus, F; Cittaro, D; Lazarevic, D; Scarselli, A; Santilli, V; Attardi, E; Stupka, E; Giannelli, S; Fraziano, M; Finocchi, A; Rossi, P; Aiuti, A; Palma, P; Cancrini, C | 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-gen-2003 | A hypermorphic I kappa B alpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency | Courtois, G; Smahi, A; Reichenbach, J; Doffinger, R; Cancrini, C; Bonnet, M; Puel, A; Chable Bessia, C; Yamaoka, S; Feinberg, J; Dupuis Girod, S; Bodemer, C; Livadiotti, S; Novelli, F; Rossi, P; Fischer, A; Israel, A; Munnich, A; Le Deist, F; Casanova, Jl | 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-2014 | A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency | Lee, Y; Frugoni, F; Dobbs, K; Walter, J; Giliani, S; Gennery, A; Al Herz, W; Haddad, E; Ledeist, F; Bleesing, J; Henderson, L; Pai, S; Nelson, R; El Ghoneimy, D; El Feky, R; Reda, S; Hossny, E; Soler Palacin, P; Fuleihan, R; Patel, N; Massaad, M; Geha, R; Puck, J; Palma, P; Cancrini, C; Chen, K; Vihinen, M; Alt, F; Notarangelo, L | Articolo su rivista | |
| 1-gen-2013 | Accumulation of peripheral autoreactive B cells in the absence of functional human regulatory T cells | Kinnunen, T; Chamberlain, N; Morbach, H; Choi, J; Kim, S; Craft, J; Mayer, L; Cancrini, C; Passerini, L; Bacchetta, R; Ochs, H; Torgerson TR and Meffre, E | Articolo su rivista | |
| 20-mag-2024 | Activated phosphoinositde 3-kinase (PI3Kδ) syndrome: an Italian point of view on diagnosis and new advances in treatment | Lougaris, V; Piane, Fl; Cancrini, C; Conti, F; Tommasini, A; Badolato, R; Trizzino, A; Zecca, M; De Rosa, A; Barzaghi, F; Pignata, C | Articolo su rivista | |
| 1-gen-2022 | Activated phosphoinositide 3-dinase delta syndrome (APDS): An update | Lougaris, V; Cancrini, C; Rivalta, B; Castagnoli, R; Giardino, G; Volpi, S; Leonardi, L; La Torre, F; Federici, S; Corrente, S; Cinicola, B; Soresina, A; Marseglia, G; Cardinale, F | 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-2016 | Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy | Cifaldi, C; Scarselli, A; Petricone, D; DI CESARE, S; Chiriaco, M; Claps, A; Rossi, P; Calzoni, E; Yamazaki, Y; Notarangelo, L; DI MATTEO, G; Cancrini, C; Finocchi, A | Articolo su rivista | |
| 1-set-2021 | Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia | Desimio, Mg; Finocchi, A; Di Matteo, G; Di Cesare, S; Giancotta, C; Conti, F; Chessa, L; Piane, M; Montin, D; Dellepiane, M; Rossi, P; Cancrini, C; Doria, M | Articolo su rivista | |
| 1-gen-1998 | Analysis of HIV-1 reverse transcriptase gene mutations in infected children treated with zidovudine | Orlandi, P; Cancrini, C; Scaccia, S; Romiti, Ml; Livadiotti, S; Gattinara, Gc; Angelini, F; Cox, S; Rossi, P | Articolo su rivista | |
| 1-ott-2013 | Anti-infective prophylaxis for primary immunodeficiencies: what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature | Moschese, V; Martire, B; Soresina, A; Chini, L; Graziani, S; Monteferrario, E; Bacchetta, R; Cancrini, C; Fiorilli, M; Gambineri, E; Pession, A; Pignata, C; Quinti, I; Rondelli, R; Rossi, P; Ugazio, A; Plebani, A; Pietrogrande, M | 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 |