CANCRINI, CATERINA
CANCRINI, CATERINA
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
[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 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 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
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
Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function
2003-07-01 Gagliardi, M; Finocchi, A; Orlandi, P; Cursi, L; Cancrini, C; Moschese, V; Miyawaki, T; Rossi, P
Caratterizzazione clinica di pazienti con ipogammaglobulinemia.
2010-01-01 Yammine, M; Conti, F; LA ROCCA, M; Silenzi, R; Chini, L; Graziani, S; Corrente, S; Freda, E; DI CESARE, S; DI MATTEO, G; Barroeta Seijas, A; Cancrini, C; Finocchi, A; Moschese, V
Caratterizzazione genetica di pazienti pediatrici con ipogammaglobulinemia.
2010-01-01 Barroeta Seijas, A; LA ROCCA, M; Conti, F; Graziani, S; Chini, L; Corrente, S; Yammine, M; Silenzi, R; Cancrini, C; Finocchi, A; Moschese, V
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up
2021-01-01 Rivalta, B; Amodio, D; Milito, C; Chiriaco, M; Di Cesare, S; Giancotta, C; Conti, F; Santilli, V; Pacillo, L; Cifaldi, C; Desimio, Mg; Doria, M; Quinti, I; De Vito, R; Di Matteo, G; Finocchi, A; Palma, P; Trizzino, A; Tommasini, A; Cancrini, C
Case Report: Successful Treatment With Monoclonal Antibodies in One APDS Patient With Prolonged SARS-CoV-2 Infection Not Responsive to Previous Lines of Treatment
2022-01-01 Rivalta, B; Amodio, D; Giancotta, C; Santilli, V; Pacillo, L; Zangari, P; Cotugno, N; Manno, Ec; Finocchi, A; Bernardi, S; Colagrossi, L; Gentile, L; Russo, C; Perno, Cf; Rossi, P; Cancrini, C; Palma, P
Characterization of T and B cell repertoire diversity in patients with RAG deficiency
2016-01-01 Lee, Yn; Frugoni, F; Dobbs, K; Tirosh, I; Du, L; Ververs, Fa; Ru, H; De Bruin, Lo; Adeli, M; Bleesing, Jh; Buchbinder, D; Butte, Mj; Cancrini, C; Chen, K; Choo, S; Elfeky, Ra; Finocchi, A; Fuleihan, Rl; Gennery, Ar; El-Ghoneimy, Dh; Henderson, La; Al-Herz, W; Hossny, E; Nelson, Rp; Pai, S-; Patel, Nc; Reda, Sm; Soler-Palacin, P; Somech, R; Palma, P; Wu, H; Giliani, S; Walter, Je; Notarangelo, Ld
| 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-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 | |
| 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-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-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 | |
| 1-lug-2003 | Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function | Gagliardi, M; Finocchi, A; Orlandi, P; Cursi, L; Cancrini, C; Moschese, V; Miyawaki, T; Rossi, P | Articolo su rivista | |
| 1-gen-2010 | Caratterizzazione clinica di pazienti con ipogammaglobulinemia. | Yammine, M; Conti, F; LA ROCCA, M; Silenzi, R; Chini, L; Graziani, S; Corrente, S; Freda, E; DI CESARE, S; DI MATTEO, G; Barroeta Seijas, A; Cancrini, C; Finocchi, A; Moschese, V | Articolo su rivista | |
| 1-gen-2010 | Caratterizzazione genetica di pazienti pediatrici con ipogammaglobulinemia. | Barroeta Seijas, A; LA ROCCA, M; Conti, F; Graziani, S; Chini, L; Corrente, S; Yammine, M; Silenzi, R; Cancrini, C; Finocchi, A; Moschese, V | Articolo su rivista | |
| 1-gen-2021 | Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up | Rivalta, B; Amodio, D; Milito, C; Chiriaco, M; Di Cesare, S; Giancotta, C; Conti, F; Santilli, V; Pacillo, L; Cifaldi, C; Desimio, Mg; Doria, M; Quinti, I; De Vito, R; Di Matteo, G; Finocchi, A; Palma, P; Trizzino, A; Tommasini, A; Cancrini, C | Articolo su rivista | |
| 1-gen-2022 | Case Report: Successful Treatment With Monoclonal Antibodies in One APDS Patient With Prolonged SARS-CoV-2 Infection Not Responsive to Previous Lines of Treatment | Rivalta, B; Amodio, D; Giancotta, C; Santilli, V; Pacillo, L; Zangari, P; Cotugno, N; Manno, Ec; Finocchi, A; Bernardi, S; Colagrossi, L; Gentile, L; Russo, C; Perno, Cf; Rossi, P; Cancrini, C; Palma, P | Articolo su rivista | |
| 1-gen-2016 | Characterization of T and B cell repertoire diversity in patients with RAG deficiency | Lee, Yn; Frugoni, F; Dobbs, K; Tirosh, I; Du, L; Ververs, Fa; Ru, H; De Bruin, Lo; Adeli, M; Bleesing, Jh; Buchbinder, D; Butte, Mj; Cancrini, C; Chen, K; Choo, S; Elfeky, Ra; Finocchi, A; Fuleihan, Rl; Gennery, Ar; El-Ghoneimy, Dh; Henderson, La; Al-Herz, W; Hossny, E; Nelson, Rp; Pai, S-; Patel, Nc; Reda, Sm; Soler-Palacin, P; Somech, R; Palma, P; Wu, H; Giliani, S; Walter, Je; Notarangelo, Ld | Articolo su rivista |