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Scalable GMP-compliant gene correction of CD4+ T cells with IDLV template functionally validated in vitro and in vivo.
Asperti C, Canarutto D, Porcellini S, Sanvito F, Cecere F, Vavassori V, Ferrari S, Rovelli E, Albano L, Jacob A, Sergi Sergi L, Montaldo E, Ferrua F, González-Granado LI, Lougaris V, Badolato R, Finocchi A, Villa A, Radrizzani M, Naldini L. Asperti C, et al. Among authors: badolato r. Mol Ther Methods Clin Dev. 2023 Aug 23;30:546-557. doi: 10.1016/j.omtm.2023.08.020. eCollection 2023 Sep 14. Mol Ther Methods Clin Dev. 2023. PMID: 37693944 Free PMC article.
Hennekam Syndrome due to a Novel Homozygous CCBE1 Mutation Presenting as Pediatric-Onset Common Variable Immune Deficiency.
Tessarin G, Baronio M, Gazzurelli L, Rossi S, Chiarini M, Moratto D, Badolato R, Lougaris V. Tessarin G, et al. Among authors: badolato r. J Investig Allergol Clin Immunol. 2023 Dec 14;33(6):488-490. doi: 10.18176/jiaci.0895. Epub 2023 Feb 7. J Investig Allergol Clin Immunol. 2023. PMID: 36748365 Free article. No abstract available.
CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis.
Baronio M, Gazzurelli L, Rezzola S, Rossi S, Tessarin G, Marinoni M, Salpietro A, Fiore M, Moratto D, Chiarini M, Badolato R, Parolini S, Tabellini G, Lougaris V. Baronio M, et al. Among authors: badolato r. Immunobiology. 2023 May;228(3):152381. doi: 10.1016/j.imbio.2023.152381. Epub 2023 Apr 5. Immunobiology. 2023. PMID: 37086690
Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job's syndrome.
Carrabba M, Dellepiane RM, Cortesi M, Baselli LA, Soresina A, Cirillo E, Giardino G, Conti F, Dotta L, Finocchi A, Cancrini C, Milito C, Pacillo L, Cinicola BL, Cossu F, Consolini R, Montin D, Quinti I, Pession A, Fabio G, Pignata C, Pietrogrande MC, Badolato R. Carrabba M, et al. Among authors: badolato r. Allergy Asthma Clin Immunol. 2023 Apr 20;19(1):32. doi: 10.1186/s13223-023-00776-5. Allergy Asthma Clin Immunol. 2023. PMID: 37081481 Free PMC article.
Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function.
Dotta L, Baresi G, Tamassia N, Calzetti F, Bianchetto-Aguilera F, Gasperini S, Gardiman E, Chiarini M, Moratto D, Martellosio G, Serana F, Micheletti M, Tregambe D, Pintabona V, Soncini E, Meini A, Girelli MF, Beghin A, Lanfranchi A, Bugatti M, Brugnoni D, Soresina A, Plebani A, Cassatella M, Vermi W, Porta F, Badolato R. Dotta L, et al. Among authors: badolato r. Pediatr Blood Cancer. 2023 Dec;70(12):e30671. doi: 10.1002/pbc.30671. Epub 2023 Sep 15. Pediatr Blood Cancer. 2023. PMID: 37712719
COVID-19 Pneumonia with Migratory Pattern in Agammaglobulinemic Patients: A Report of Two Cases and Review of Literature.
Degli Antoni M, Crosato V, Pennati F, Borghesi A, Cristini G, Allegri R, Capone S, Bergamasco A, Soresina A, Badolato R, Maroldi R, Quiros-Roldan E, Matteelli A, Castelli F, Focà E. Degli Antoni M, et al. Among authors: badolato r. Tomography. 2023 Apr 23;9(3):894-900. doi: 10.3390/tomography9030073. Tomography. 2023. PMID: 37218933 Free PMC article. Review.
Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation.
Sbrini G, Tomasoni Z, Cutrì MR, Pilotta A, Mingotti C, Badolato R, La Via L, Barbon A, Bono F, Fiorentini C. Sbrini G, et al. Among authors: badolato r. Stem Cell Res. 2024 Feb;74:103293. doi: 10.1016/j.scr.2023.103293. Epub 2023 Dec 28. Stem Cell Res. 2024. PMID: 38160629 Free article.
237 results