Sfoglia per Autore
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
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment
2017-05-01 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
Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome?
2017-05-02 Moscato, G; Giacobbi, E; Anemona, L; DI CESARE, S; DI MATTEO, G; Andreoni, M; Mauriello, A; Moschese, V; Chini, L
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene
2018-01-01 Di Matteo, G; Chiriaco, ; M. Scarselli A., Cc; Livadiotti, S; Di Cesare, S; Ferradini, V; Aiuti, A; Rossi, P; Finocchi, A; Cancrini, C
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene
2018-01-01 Di Matteo, G; Chiriaco, M; Scarselli, A; Cifaldi, C; Livadiotti, S; Di Cesare, S; Ferradini, V; Aiuti, A; Rossi, P; Finocchi, A; Cancrini, C
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent
2018-01-01 Chiriaco, M; Casciano, F; Di Matteo, G; Gentner, B; Claps, A; Di Cesare, S; Cotugno, N; D'Argenio, P; Rossi, P; Aiuti, A; Finocchi, A
Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment.
2019-01-01 Zangari, P; Cifaldi, C; Di Cesare, S; Di Matteo, G; Chiriaco, M; Amodio, D; Cotugno, N; De Luca, M; Surace, C; Ladogana, S; Gardini, S; Merli, P; Algeri, M; Rossi, P; Palma, P; Cancrini, C; Finocchi, 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
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies
2019-01-01 Cifaldi, C; Brigida, I; Barzaghi, F; Zoccolillo, M; Ferradini, V; Petricone, D; Cicalese, Mp; Lazarevic, D; Cittaro, D; Omrani, M; Attardi, E; Conti, F; Scarselli, A; Chiriaco, M; Di Cesare, S; Licciardi, F; Forin, Dm; Ferrua, F; Canessa, C; Pignata, C; Giliani, S; Ferrari, S; Fousteri, G; Barera, G; Merli, P; Palma, P; Cesaro, S; Gattorno, M; Trizzino, A; Moschese, V; Chini, L; Villa, A; Azzari, C; Finocchi, A; Locatelli, F; Rossi, P; Sangiuolo, F; Aiuti, A; Cancrini, C; Di Matteo, G
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome
2019-01-01 Montin, D; Marolda, A; Licciardi, F; Robasto, F; Di Cesare, S; Ricotti, E; Ferro, F; Scaioli, G; Giancotta, C; Amodio, D; Conti, F; Giardino, G; Leonardi, L; Ricci, S; Volpi, S; Baselli, La; Azzari, C; Bossi, G; Consolini, R; Dellepiane, Rm; Duse, M; Gattorno, M; Martire, B; Putti, Mc; Soresina, A; Plebani, A; Ramenghi, U; Martino, S; Pignata, C; Cancrini, C
Regulation of Kit Expression in Early Mouse Embryos and ES Cells
2019-01-01 Todaro, F; Campolo, F; Barrios, F; Pellegrini, M; Di Cesare, S; Tessarollo, L; Rossi, P; Jannini, Ea; Dolci, S
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children
2019-01-01 Moschese, V; Chini, L; Graziani, S; Sgrulletti, M; Gallo, V; Di Matteo, G; Ferrari, S; Di Cesare, S; Cirillo, E; Pession, A; Pignata, C; Specchia, F
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia
2019-02-01 Chiriaco, M; Di Matteo, G; Conti, F; Petricone, D; De Luca, M; Di Cesare, S; Cifaldi, C; De Vito, R; Zoccolillo, M; Serafinelli, J; Poerio, N; Fraziano, M; Brigida, I; Cardinale, F; Rossi, P; Aiuti, A; Cancrini, C; Finocchi, A
Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene
2020-01-01 Cifaldi, C; Cotugno, N; Di Cesare, S; Giliani, S; Di Matteo, G; Amodio, D; Piano Mortari, E; Chiriaco, M; Buonsenso, D; Zangari, P; Pagliara, D; Gaspari, S; Carsetti, R; Palma, P; Finocchi, A; Locatelli, F; Rossi, P; Doria, M; Cancrini, C
Early ART-treated perinatally HIV-infected seronegative children demonstrate distinct long-term persistence of HIV-specific T and B cell memory
2020-01-01 Cotugno, N; Morrocchi, E; Rinaldi, S; Rocca, S; Pepponi, I; di Cesare, S; Bernardi, S; Zangari, P; Pallikkuth, S; de Armas, L; Levy, O; Rossi, P; Pahwa, S; Palma, P
Seletalisib for activated PI3Kδ syndromes: open-label phase 1b and extension studies
2020-12-15 Diaz, N; Juarez, M; Cancrini, C; Heeg, M; Soler-Palacín, P; Payne, A; Johnston, G; Helmer, E; Cain, D; Mann, J; Yuill, D; Conti, F; Di Cesare, S; Ehl, S; Garcia-Prat, M; Maccari, M; Martín-Nalda, A; Martínez-Gallo, M; Moshous, D; Santilli, V; Semeraro, M; Simonetti, A; Suarez, F; Cavazzana, M; Kracker, S
Thymosin Alpha 1 Mitigates Cytokine Storm in Blood Cells From Coronavirus Disease 2019 Patients
2021-01-01 Matteucci, C; Minutolo, A; Balestrieri, E; Petrone, V; Fanelli, M; Malagnino, V; Iannetta, M; Giovinazzo, A; Barreca, F; Di Cesare, S; De Marco, P; Miele, M; Toschi, N; Mastino, A; Vallebona, P; Bernardini, S; Rogliani, P; Sarmati, L; Andreoni, M; Grelli, S; Garaci, E
Immunological aspects of x-linked chronic granulomatous disease female carriers
2021-01-01 Chiriaco, M; Salfa, I; Ursu, Gm; Cifaldi, C; Di Cesare, S; Rossi, P; Di Matteo, G; Finocchi, A
Author Correction: Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome (Scientific Reports, (2017), 7, 1, (12297), 10.1038/s41598-017-12069-0)
2021-01-01 Sbardella, D; Tundo, Gr; Campagnolo, L; Valacchi, G; Orlandi, A; Curatolo, P; Borsellino, G; D?esposito, M; Ciaccio, C; Di Cesare, S; Pierro, Dd; Galasso, C; Santarone, Me; Hayek, J; Coletta, M; Marini, S
Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature
2021-01-01 Romani, L; Williamson, P; Di Cesare, S; Di Matteo, G; De Luca, M; Carsetti, R; Figà-Talamanca, L; Cancrini, C; Rossi, P; Finocchi A 10. 3389/fimmu. 2021., 7
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 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-mag-2017 | The case of an 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 | |
| 2-mag-2017 | Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome? | Moscato, G; Giacobbi, E; Anemona, L; DI CESARE, S; DI MATTEO, G; Andreoni, M; Mauriello, A; Moschese, V; Chini, L | Articolo su rivista | |
| 1-gen-2018 | JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene | Di Matteo, G; Chiriaco, ; M. Scarselli A., Cc; Livadiotti, S; Di Cesare, S; Ferradini, V; Aiuti, A; Rossi, P; Finocchi, A; Cancrini, C | Articolo su rivista | |
| 1-gen-2018 | JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene | Di Matteo, G; Chiriaco, M; Scarselli, A; Cifaldi, C; Livadiotti, S; Di Cesare, S; Ferradini, V; Aiuti, A; Rossi, P; Finocchi, A; Cancrini, C | Articolo su rivista | |
| 1-gen-2018 | Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent | Chiriaco, M; Casciano, F; Di Matteo, G; Gentner, B; Claps, A; Di Cesare, S; Cotugno, N; D'Argenio, P; Rossi, P; Aiuti, A; Finocchi, A | Articolo su rivista | |
| 1-gen-2019 | Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment. | Zangari, P; Cifaldi, C; Di Cesare, S; Di Matteo, G; Chiriaco, M; Amodio, D; Cotugno, N; De Luca, M; Surace, C; Ladogana, S; Gardini, S; Merli, P; Algeri, M; Rossi, P; Palma, P; Cancrini, C; Finocchi, 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-gen-2019 | Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies | Cifaldi, C; Brigida, I; Barzaghi, F; Zoccolillo, M; Ferradini, V; Petricone, D; Cicalese, Mp; Lazarevic, D; Cittaro, D; Omrani, M; Attardi, E; Conti, F; Scarselli, A; Chiriaco, M; Di Cesare, S; Licciardi, F; Forin, Dm; Ferrua, F; Canessa, C; Pignata, C; Giliani, S; Ferrari, S; Fousteri, G; Barera, G; Merli, P; Palma, P; Cesaro, S; Gattorno, M; Trizzino, A; Moschese, V; Chini, L; Villa, A; Azzari, C; Finocchi, A; Locatelli, F; Rossi, P; Sangiuolo, F; Aiuti, A; Cancrini, C; Di Matteo, G | Articolo su rivista | |
| 1-gen-2019 | Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome | Montin, D; Marolda, A; Licciardi, F; Robasto, F; Di Cesare, S; Ricotti, E; Ferro, F; Scaioli, G; Giancotta, C; Amodio, D; Conti, F; Giardino, G; Leonardi, L; Ricci, S; Volpi, S; Baselli, La; Azzari, C; Bossi, G; Consolini, R; Dellepiane, Rm; Duse, M; Gattorno, M; Martire, B; Putti, Mc; Soresina, A; Plebani, A; Ramenghi, U; Martino, S; Pignata, C; Cancrini, C | Articolo su rivista | |
| 1-gen-2019 | Regulation of Kit Expression in Early Mouse Embryos and ES Cells | Todaro, F; Campolo, F; Barrios, F; Pellegrini, M; Di Cesare, S; Tessarollo, L; Rossi, P; Jannini, Ea; Dolci, S | Articolo su rivista | |
| 1-gen-2019 | Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children | Moschese, V; Chini, L; Graziani, S; Sgrulletti, M; Gallo, V; Di Matteo, G; Ferrari, S; Di Cesare, S; Cirillo, E; Pession, A; Pignata, C; Specchia, F | Articolo su rivista | |
| 1-feb-2019 | First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia | Chiriaco, M; Di Matteo, G; Conti, F; Petricone, D; De Luca, M; Di Cesare, S; Cifaldi, C; De Vito, R; Zoccolillo, M; Serafinelli, J; Poerio, N; Fraziano, M; Brigida, I; Cardinale, F; Rossi, P; Aiuti, A; Cancrini, C; Finocchi, A | Articolo su rivista | |
| 1-gen-2020 | Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene | Cifaldi, C; Cotugno, N; Di Cesare, S; Giliani, S; Di Matteo, G; Amodio, D; Piano Mortari, E; Chiriaco, M; Buonsenso, D; Zangari, P; Pagliara, D; Gaspari, S; Carsetti, R; Palma, P; Finocchi, A; Locatelli, F; Rossi, P; Doria, M; Cancrini, C | Articolo su rivista | |
| 1-gen-2020 | Early ART-treated perinatally HIV-infected seronegative children demonstrate distinct long-term persistence of HIV-specific T and B cell memory | Cotugno, N; Morrocchi, E; Rinaldi, S; Rocca, S; Pepponi, I; di Cesare, S; Bernardi, S; Zangari, P; Pallikkuth, S; de Armas, L; Levy, O; Rossi, P; Pahwa, S; Palma, P | Articolo su rivista | |
| 15-dic-2020 | Seletalisib for activated PI3Kδ syndromes: open-label phase 1b and extension studies | Diaz, N; Juarez, M; Cancrini, C; Heeg, M; Soler-Palacín, P; Payne, A; Johnston, G; Helmer, E; Cain, D; Mann, J; Yuill, D; Conti, F; Di Cesare, S; Ehl, S; Garcia-Prat, M; Maccari, M; Martín-Nalda, A; Martínez-Gallo, M; Moshous, D; Santilli, V; Semeraro, M; Simonetti, A; Suarez, F; Cavazzana, M; Kracker, S | Articolo su rivista | |
| 1-gen-2021 | Thymosin Alpha 1 Mitigates Cytokine Storm in Blood Cells From Coronavirus Disease 2019 Patients | Matteucci, C; Minutolo, A; Balestrieri, E; Petrone, V; Fanelli, M; Malagnino, V; Iannetta, M; Giovinazzo, A; Barreca, F; Di Cesare, S; De Marco, P; Miele, M; Toschi, N; Mastino, A; Vallebona, P; Bernardini, S; Rogliani, P; Sarmati, L; Andreoni, M; Grelli, S; Garaci, E | Articolo su rivista | |
| 1-gen-2021 | Immunological aspects of x-linked chronic granulomatous disease female carriers | Chiriaco, M; Salfa, I; Ursu, Gm; Cifaldi, C; Di Cesare, S; Rossi, P; Di Matteo, G; Finocchi, A | Articolo su rivista | |
| 1-gen-2021 | Author Correction: Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome (Scientific Reports, (2017), 7, 1, (12297), 10.1038/s41598-017-12069-0) | Sbardella, D; Tundo, Gr; Campagnolo, L; Valacchi, G; Orlandi, A; Curatolo, P; Borsellino, G; D?esposito, M; Ciaccio, C; Di Cesare, S; Pierro, Dd; Galasso, C; Santarone, Me; Hayek, J; Coletta, M; Marini, S | Articolo su rivista | |
| 1-gen-2021 | Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature | Romani, L; Williamson, P; Di Cesare, S; Di Matteo, G; De Luca, M; Carsetti, R; Figà-Talamanca, L; Cancrini, C; Rossi, P; Finocchi A 10. 3389/fimmu. 2021., 7 | Articolo su rivista |
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