BARZAGHI, FEDERICA
BARZAGHI, FEDERICA
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 Novel Assay in Whole Blood Demonstrates Restoration of Mitochondrial Activity in Phagocytes After Successful HSCT in Hyperinflamed X-Linked Chronic Granulomatous Disease
2022-11-01 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
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-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
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for the diagnosis of inborn errors of immunity (IEI)
2024-11-30 Giardino, G; Di Matteo, G; Giliani, S; Ferrari, S; Lougaris, V; Badolato, R; Conti, F; Romano, R; Cicalese, Mp; Ricci, S; Barzaghi, F; Marzollo, A; Cifaldi, C; Montin, D; Lodi, L; Cirillo, E; Martire, B; Trizzino, A; Sgrulletti, M; Moschese, V; Comegna, M; Castaldo, G; Tommasini, A; Azzari, C; Cancrini, C; Aiuti, A; Pignata, C
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
Corrigendum : Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies (Frontiers in Immunology (2019) 10 (316) DOI: 10.3389/fimmu.2019.00316)
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; Cesare, Sd; Licciardi, F; Davide, M; 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
Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN Survey
2023-01-01 Muskan, I; Bethany, N; Nizar, M; Laura, O; Linda, R; Helen, L; Georgia, H; Mojca Zajc, A; Aurelien, G; Virgil, D; Rachel, R; Leire, S; Carlotta, V; Andrew R, G; Stephanie, S; Julia, N; Klaus, W; Anne-Sophie, K; Jordi, A; Marco, C; Tania, A; Stephan, B; Pere, S; Siobhan O, B; Mari, C; Transition Working Group Consortium (C Wouters, R; Meyts, I; E van der Werff Ten Bosch, J; Goffin, L; Ogunjimi, B; Gilliaux, O; Kelecic, J; Jelusic, M; Fingerhutová, S; Sediva, A; Herlin, T; J Seppänen Mikko, R; Aalto, K; Ritterbusch, H; Insalaco, A; Moschese, V; Plebani, A; Cimaz, R; Canessa, C; M Dellepiane, R; Carrabba, M; Barzaghi, F; M van Laar, Ja; M Wulffraat, N; Marques, L; Carreras, C; Sánchez-Manubens, J; Alsina, L; E Seoane Reula, M; Mendez-Echevarria, A; I Gonzales-Granado, L; Santamaria, M; Neth, O; Ekwall, O; Brodszki, O; Hague, H; A Devlin, L; Brogan, P; D Arkwright, P; Riordan, A; Mccann, L; Mcdermott, E; N Faust, S; Carne), E
Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency
2024-02-01 Migliavacca, M; Barzaghi, F; Fossati, C; Rancoita, Pmv; Gabaldo, M; Dionisio, F; Giannelli, S; Salerio, Fa; Ferrua, F; Tucci, F; Calbi, V; Gallo, V; Recupero, S; Consiglieri, G; Pajno, R; Sambuco, M; Priolo, A; Ferri, C; Garella, V; Monti, I; Silvani, P; Darin, S; Casiraghi, M; Corti, A; Zancan, S; Levi, M; Cesana, D; Carlucci, F; Pituch-Noworolska, A; Abdelaziz, D; Baumann, U; Finocchi, A; Cancrini, C; Ladogana, S; Meinhardt, A; Meyts, I; Montin, D; Notarangelo, Ld; Porta, F; Pasquet, M; Speckmann, C; Stepensky, P; Tommasini, A; Rabusin, M; Karakas, Z; Galicchio, M; Leonardi, L; Duse, M; Guner, Sn; Di Serio, C; Ciceri, F; Bernardo, Me; Aiuti, A; Cicalese, Mp
Natural history of Ras-associated autoimmune leukoproliferative disorder: A 20-year follow-up of a NRAS-mutated patient excluding a malignant progression
2023-11-27 Rivalta, B; Attardi, E; Cifaldi, C; Rosti, V; Pacillo, L; Hajrullaj, H; Di , ; Cesare, S; Amodio, D; Algeri, M; Luciani, M; Barzaghi, F; Finocchi, A; Di , ; Matteo, G; Aiuti, A; Locatelli, F; Voso, Mt; Palumbo, G; Cancrini, C
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report
2022-01-01 Di Lorenzo, B; Pacillo, L; Milardi, G; Jofra, T; Di Cesare, S; Gerosa, J; Marzinotto, I; Zapparoli, E; Rivalta, B; Cifaldi, C; Barzaghi, F; Giancotta, C; Zangari, P; Rapini, N; Deodati, A; Amodio, G; Passerini, L; Carrera, P; Gregori, S; Palma, P; Finocchi, A; Lampasona, V; Cicalese, M; Schiaffini, R; Di Matteo, G; Merelli, I; Barcella, M; Aiuti, A; Piemonti, L; Cancrini, C; Fousteri G. 10. 3389/fimmu., 2
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
2023-04-05 Matuozzo, D; Talouarn, E; Marchal, A; Zhang, P; Manry, J; Seeleuthner, Y; Zhang, Y; Bolze, A; Chaldebas, M; Milisavljevic, B; Gervais, A; Bastard, P; Asano, T; Bizien, L; Barzaghi, F; Abolhassani, H; Abou Tayoun, A; Aiuti, A; Alavi Darazam, I; Allende, Lm; Alonso-Arias, R; Arias, Aa; Aytekin, G; Bergman, P; Bondesan, S; Bryceson, Yt; Bustos, Ig; Cabrera-Marante, O; Carcel, S; Carrera, P; Casari, G; Chaïbi, K; Colobran, R; Condino-Neto, A; Covill, Le; Delmonte, Om; El Zein, L; Flores, C; Gregersen, Pk; Gut, M; Haerynck, F; Halwani, R; Hancerli, S; Hammarström, L; Hatipoğlu, N; Karbuz, A; Keles, S; Kyheng, C; Leon-Lopez, R; Franco, Jl; Mansouri, D; Martinez-Picado, J; Metin Akcan, O; Migeotte, I; Morange, P; Morelle, G; Martin-Nalda, A; Novelli, G; Novelli, A; Ozcelik, T; Palabiyik, F; Pan-Hammarström, Q; de Diego, Rp; Planas-Serra, L; Pleguezuelo, De; Prando, C; Pujol, A; Reyes, Lf; Rivière, Jg; Rodriguez-Gallego, C; Rojas, J; Rovere-Querini, P; Schlüter, A; Shahrooei, M; Sobh, A; Soler-Palacin, P; Tandjaoui-Lambiotte, Y; Tipu, I; Tresoldi, C; Troya, J; van de Beek, D; Zatz, M; Zawadzki, P; Al-Muhsen, Sz; Alosaimi, Mf; Alsohime, Fm; Baris-Feldman, H; Butte, Mj; Constantinescu, Sn; Cooper, Ma; Dalgard, Cl; Fellay, J; Heath, Jr; Lau, Y; Lifton, Rp; Maniatis, T; Mogensen, Th; von Bernuth, H; Lermine, A; Vidaud, M; Boland, A; Deleuze, J; Nussbaum, R; Kahn-Kirby, A; Mentre, F; Tubiana, S; Gorochov, G; Tubach, F; Hausfater, P; Meyts, I; Zhang, S; Puel, A; Notarangelo, Ld; Boisson-Dupuis, S; Su, Hc; Boisson, B; Jouanguy, E; Casanova, J; Zhang, Q; Abel, L; Cobat, A
Rituximab unveils hypogammaglobulinemia and immunodeficiency in children with autoimmune cytopenia
2020-01-01 Ottaviano, G; Marinoni, M; Graziani, S; Sibson, K; Barzaghi, F; Bertolini, P; Chini, L; Corti, P; Cancrini, C; D'Alba, I; Gabelli, M; Gallo, V; Giancotta, C; Giordano, P; Lassandro, G; Martire, B; Angarano, R; Mastrodicasa, E; Bava, C; Miano, M; Naviglio, S; Verzegnassi, F; Saracco, P; Trizzino, A; Biondi, A; Pignata, C; Moschese, V
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
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies. Front Immunol. 2019 Apr 11;10:316. doi: 10.3389/fimmu.2019.00316. eCollection 2019. Erratum in: Front Immunol. 2019 May 31;10:1184.
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; Cesare, Sd; Licciardi, F; Davide, M; 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
Urogenital Abnormalities in Adenosine Deaminase Deficiency
2020-01-01 Pajno, R; Pacillo, L; Recupero, S; Cicalese, Mp; Ferrua, F; Barzaghi, F; Ricci, S; Marzollo, A; Pecorelli, S; Azzari, C; Finocchi, A; Cancrini, C; Di Matteo, G; Russo, G; Alfano, M; Lesma, A; Salonia, A; Adams, S; Booth, C; Aiuti, A
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19
2021-08-01 Asano, T; Boisson, B; Onodi, F; Matuozzo, D; Moncada-Velez, M; Maglorius Renkilaraj, Mrl; Zhang, P; Meertens, L; Bolze, A; Materna, M; Korniotis, S; Gervais, A; Talouarn, E; Bigio, B; Seeleuthner, Y; Bilguvar, K; Zhang, Y; Neehus, A; Ogishi, M; Pelham, Sj; Le Voyer, T; Rosain, J; Philippot, Q; Soler-Palacín, P; Colobran, R; Martin-Nalda, A; Rivière, Jg; Tandjaoui-Lambiotte, Y; Chaïbi, K; Shahrooei, M; Darazam, Ia; Olyaei, Na; Mansouri, D; Hatipoğlu, N; Palabiyik, F; Ozcelik, T; Novelli, G; Novelli, A; Casari, G; Aiuti, A; Carrera, P; Bondesan, S; Barzaghi, F; Rovere-Querini, P; Tresoldi, C; Franco, Jl; Rojas, J; Reyes, Lf; Bustos, Ig; Arias, Aa; Morelle, G; Christèle, K; Troya, J; Planas-Serra, L; Schlüter, A; Gut, M; Pujol, A; Allende, Lm; Rodriguez-Gallego, C; Flores, C; Cabrera-Marante, O; Pleguezuelo, De; de Diego, Rp; Keles, S; Aytekin, G; Akcan, Om; Bryceson, Yt; Bergman, P; Brodin, P; Smole, D; Smith, Cie; Norlin, A; Campbell, Tm; Covill, Le; Hammarström, L; Pan-Hammarström, Q; Abolhassani, H; Mane, S; Marr, N; Ata, M; Al Ali, F; Khan, T; Spaan, An; Dalgard, Cl; Bonfanti, P; Biondi, A; Tubiana, S; Burdet, C; Nussbaum, R; Kahn-Kirby, A; Snow, Al; Bustamante, J; Puel, A; Boisson-Dupuis, S; Zhang, S; Béziat, V; Lifton, Rp; Bastard, P; Notarangelo, Ld; Abel, L; Su, Hc; Jouanguy, E; Amara, A; Soumelis, V; Cobat, A; Zhang, Q; Casanova, J
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
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 | |
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-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 | |
30-nov-2024 | Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for the diagnosis of inborn errors of immunity (IEI) | Giardino, G; Di Matteo, G; Giliani, S; Ferrari, S; Lougaris, V; Badolato, R; Conti, F; Romano, R; Cicalese, Mp; Ricci, S; Barzaghi, F; Marzollo, A; Cifaldi, C; Montin, D; Lodi, L; Cirillo, E; Martire, B; Trizzino, A; Sgrulletti, M; Moschese, V; Comegna, M; Castaldo, G; Tommasini, A; Azzari, C; Cancrini, C; Aiuti, A; Pignata, C | 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-gen-2019 | Corrigendum : Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies (Frontiers in Immunology (2019) 10 (316) DOI: 10.3389/fimmu.2019.00316) | 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; Cesare, Sd; Licciardi, F; Davide, M; 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-2023 | Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN Survey | Muskan, I; Bethany, N; Nizar, M; Laura, O; Linda, R; Helen, L; Georgia, H; Mojca Zajc, A; Aurelien, G; Virgil, D; Rachel, R; Leire, S; Carlotta, V; Andrew R, G; Stephanie, S; Julia, N; Klaus, W; Anne-Sophie, K; Jordi, A; Marco, C; Tania, A; Stephan, B; Pere, S; Siobhan O, B; Mari, C; Transition Working Group Consortium (C Wouters, R; Meyts, I; E van der Werff Ten Bosch, J; Goffin, L; Ogunjimi, B; Gilliaux, O; Kelecic, J; Jelusic, M; Fingerhutová, S; Sediva, A; Herlin, T; J Seppänen Mikko, R; Aalto, K; Ritterbusch, H; Insalaco, A; Moschese, V; Plebani, A; Cimaz, R; Canessa, C; M Dellepiane, R; Carrabba, M; Barzaghi, F; M van Laar, Ja; M Wulffraat, N; Marques, L; Carreras, C; Sánchez-Manubens, J; Alsina, L; E Seoane Reula, M; Mendez-Echevarria, A; I Gonzales-Granado, L; Santamaria, M; Neth, O; Ekwall, O; Brodszki, O; Hague, H; A Devlin, L; Brogan, P; D Arkwright, P; Riordan, A; Mccann, L; Mcdermott, E; N Faust, S; Carne), E | Articolo su rivista | |
1-feb-2024 | Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency | Migliavacca, M; Barzaghi, F; Fossati, C; Rancoita, Pmv; Gabaldo, M; Dionisio, F; Giannelli, S; Salerio, Fa; Ferrua, F; Tucci, F; Calbi, V; Gallo, V; Recupero, S; Consiglieri, G; Pajno, R; Sambuco, M; Priolo, A; Ferri, C; Garella, V; Monti, I; Silvani, P; Darin, S; Casiraghi, M; Corti, A; Zancan, S; Levi, M; Cesana, D; Carlucci, F; Pituch-Noworolska, A; Abdelaziz, D; Baumann, U; Finocchi, A; Cancrini, C; Ladogana, S; Meinhardt, A; Meyts, I; Montin, D; Notarangelo, Ld; Porta, F; Pasquet, M; Speckmann, C; Stepensky, P; Tommasini, A; Rabusin, M; Karakas, Z; Galicchio, M; Leonardi, L; Duse, M; Guner, Sn; Di Serio, C; Ciceri, F; Bernardo, Me; Aiuti, A; Cicalese, Mp | Articolo su rivista | |
27-nov-2023 | Natural history of Ras-associated autoimmune leukoproliferative disorder: A 20-year follow-up of a NRAS-mutated patient excluding a malignant progression | Rivalta, B; Attardi, E; Cifaldi, C; Rosti, V; Pacillo, L; Hajrullaj, H; Di , ; Cesare, S; Amodio, D; Algeri, M; Luciani, M; Barzaghi, F; Finocchi, A; Di , ; Matteo, G; Aiuti, A; Locatelli, F; Voso, Mt; Palumbo, G; Cancrini, C | Articolo su rivista | |
1-gen-2022 | Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report | Di Lorenzo, B; Pacillo, L; Milardi, G; Jofra, T; Di Cesare, S; Gerosa, J; Marzinotto, I; Zapparoli, E; Rivalta, B; Cifaldi, C; Barzaghi, F; Giancotta, C; Zangari, P; Rapini, N; Deodati, A; Amodio, G; Passerini, L; Carrera, P; Gregori, S; Palma, P; Finocchi, A; Lampasona, V; Cicalese, M; Schiaffini, R; Di Matteo, G; Merelli, I; Barcella, M; Aiuti, A; Piemonti, L; Cancrini, C; Fousteri G. 10. 3389/fimmu., 2 | Articolo su rivista | |
5-apr-2023 | Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 | Matuozzo, D; Talouarn, E; Marchal, A; Zhang, P; Manry, J; Seeleuthner, Y; Zhang, Y; Bolze, A; Chaldebas, M; Milisavljevic, B; Gervais, A; Bastard, P; Asano, T; Bizien, L; Barzaghi, F; Abolhassani, H; Abou Tayoun, A; Aiuti, A; Alavi Darazam, I; Allende, Lm; Alonso-Arias, R; Arias, Aa; Aytekin, G; Bergman, P; Bondesan, S; Bryceson, Yt; Bustos, Ig; Cabrera-Marante, O; Carcel, S; Carrera, P; Casari, G; Chaïbi, K; Colobran, R; Condino-Neto, A; Covill, Le; Delmonte, Om; El Zein, L; Flores, C; Gregersen, Pk; Gut, M; Haerynck, F; Halwani, R; Hancerli, S; Hammarström, L; Hatipoğlu, N; Karbuz, A; Keles, S; Kyheng, C; Leon-Lopez, R; Franco, Jl; Mansouri, D; Martinez-Picado, J; Metin Akcan, O; Migeotte, I; Morange, P; Morelle, G; Martin-Nalda, A; Novelli, G; Novelli, A; Ozcelik, T; Palabiyik, F; Pan-Hammarström, Q; de Diego, Rp; Planas-Serra, L; Pleguezuelo, De; Prando, C; Pujol, A; Reyes, Lf; Rivière, Jg; Rodriguez-Gallego, C; Rojas, J; Rovere-Querini, P; Schlüter, A; Shahrooei, M; Sobh, A; Soler-Palacin, P; Tandjaoui-Lambiotte, Y; Tipu, I; Tresoldi, C; Troya, J; van de Beek, D; Zatz, M; Zawadzki, P; Al-Muhsen, Sz; Alosaimi, Mf; Alsohime, Fm; Baris-Feldman, H; Butte, Mj; Constantinescu, Sn; Cooper, Ma; Dalgard, Cl; Fellay, J; Heath, Jr; Lau, Y; Lifton, Rp; Maniatis, T; Mogensen, Th; von Bernuth, H; Lermine, A; Vidaud, M; Boland, A; Deleuze, J; Nussbaum, R; Kahn-Kirby, A; Mentre, F; Tubiana, S; Gorochov, G; Tubach, F; Hausfater, P; Meyts, I; Zhang, S; Puel, A; Notarangelo, Ld; Boisson-Dupuis, S; Su, Hc; Boisson, B; Jouanguy, E; Casanova, J; Zhang, Q; Abel, L; Cobat, A | Articolo su rivista | |
1-gen-2020 | Rituximab unveils hypogammaglobulinemia and immunodeficiency in children with autoimmune cytopenia | Ottaviano, G; Marinoni, M; Graziani, S; Sibson, K; Barzaghi, F; Bertolini, P; Chini, L; Corti, P; Cancrini, C; D'Alba, I; Gabelli, M; Gallo, V; Giancotta, C; Giordano, P; Lassandro, G; Martire, B; Angarano, R; Mastrodicasa, E; Bava, C; Miano, M; Naviglio, S; Verzegnassi, F; Saracco, P; Trizzino, A; Biondi, A; Pignata, C; Moschese, V | 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 | Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies. Front Immunol. 2019 Apr 11;10:316. doi: 10.3389/fimmu.2019.00316. eCollection 2019. Erratum in: Front Immunol. 2019 May 31;10:1184. | 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; Cesare, Sd; Licciardi, F; Davide, M; 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-2020 | Urogenital Abnormalities in Adenosine Deaminase Deficiency | Pajno, R; Pacillo, L; Recupero, S; Cicalese, Mp; Ferrua, F; Barzaghi, F; Ricci, S; Marzollo, A; Pecorelli, S; Azzari, C; Finocchi, A; Cancrini, C; Di Matteo, G; Russo, G; Alfano, M; Lesma, A; Salonia, A; Adams, S; Booth, C; Aiuti, A | Articolo su rivista | |
1-ago-2021 | X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19 | Asano, T; Boisson, B; Onodi, F; Matuozzo, D; Moncada-Velez, M; Maglorius Renkilaraj, Mrl; Zhang, P; Meertens, L; Bolze, A; Materna, M; Korniotis, S; Gervais, A; Talouarn, E; Bigio, B; Seeleuthner, Y; Bilguvar, K; Zhang, Y; Neehus, A; Ogishi, M; Pelham, Sj; Le Voyer, T; Rosain, J; Philippot, Q; Soler-Palacín, P; Colobran, R; Martin-Nalda, A; Rivière, Jg; Tandjaoui-Lambiotte, Y; Chaïbi, K; Shahrooei, M; Darazam, Ia; Olyaei, Na; Mansouri, D; Hatipoğlu, N; Palabiyik, F; Ozcelik, T; Novelli, G; Novelli, A; Casari, G; Aiuti, A; Carrera, P; Bondesan, S; Barzaghi, F; Rovere-Querini, P; Tresoldi, C; Franco, Jl; Rojas, J; Reyes, Lf; Bustos, Ig; Arias, Aa; Morelle, G; Christèle, K; Troya, J; Planas-Serra, L; Schlüter, A; Gut, M; Pujol, A; Allende, Lm; Rodriguez-Gallego, C; Flores, C; Cabrera-Marante, O; Pleguezuelo, De; de Diego, Rp; Keles, S; Aytekin, G; Akcan, Om; Bryceson, Yt; Bergman, P; Brodin, P; Smole, D; Smith, Cie; Norlin, A; Campbell, Tm; Covill, Le; Hammarström, L; Pan-Hammarström, Q; Abolhassani, H; Mane, S; Marr, N; Ata, M; Al Ali, F; Khan, T; Spaan, An; Dalgard, Cl; Bonfanti, P; Biondi, A; Tubiana, S; Burdet, C; Nussbaum, R; Kahn-Kirby, A; Snow, Al; Bustamante, J; Puel, A; Boisson-Dupuis, S; Zhang, S; Béziat, V; Lifton, Rp; Bastard, P; Notarangelo, Ld; Abel, L; Su, Hc; Jouanguy, E; Amara, A; Soumelis, V; Cobat, A; Zhang, Q; Casanova, J | Articolo su rivista |