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Impaired arterial dilation and increased NOX2 generated oxidative stress in subjects with ataxia-telangiectasia mutated (ATM) kinase.
Loffredo L, Soresina A, Cinicola BL, Capponi M, Salvatori F, Bartimoccia S, Picchio V, Forte M, Caputi C, Poscia R, Leuzzi V, Spalice A, Pignatelli P, Badolato R, Duse M, Violi F, Carnevale R, Zicari AM; AT study group. Loffredo L, et al. Among authors: badolato r. Redox Biol. 2024 Nov;77:103347. doi: 10.1016/j.redox.2024.103347. Epub 2024 Sep 12. Redox Biol. 2024. PMID: 39326070 Free PMC article.
In adult X-CGD patients, regulatory T cells are expanded while activated T cells display a NOX2-independent ROS increase.
Cammarata I, Pinna V, Pacella I, Rotella I, Soresina A, Badolato R, Plebani A, Pignata C, Cirillo E, Zicari AM, Violi F, Carnevale R, Loffredo L, Piconese S. Cammarata I, et al. Among authors: badolato r. Immunol Lett. 2024 Apr;266:106839. doi: 10.1016/j.imlet.2024.106839. Epub 2024 Feb 1. Immunol Lett. 2024. PMID: 38309375 Free article.
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.
MicroRNA dysregulation in ataxia telangiectasia.
Cirillo E, Tarallo A, Toriello E, Carissimo A, Giardino G, De Rosa A, Damiano C, Soresina A, Badolato R, Dellepiane RM, Baselli LA, Carrabba M, Fabio G, Bertolini P, Montin D, Conti F, Romano R, Pozzi E, Ferrero G, Roncarati R, Ferracin M, Brusco A, Parenti G, Pignata C. Cirillo E, et al. Among authors: badolato r. Front Immunol. 2024 Aug 19;15:1444130. doi: 10.3389/fimmu.2024.1444130. eCollection 2024. Front Immunol. 2024. PMID: 39224604 Free PMC article.
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.
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
Adolescent gender dysphoria management: position paper from the Italian Academy of Pediatrics, the Italian Society of Pediatrics, the Italian Society for Pediatric Endocrinology and Diabetes, the Italian Society of Adolescent Medicine and the Italian Society of Child and Adolescent Neuropsychiatry.
Calcaterra V, Tornese G, Zuccotti G, Staiano A, Cherubini V, Gaudino R, Fazzi EM, Barbi E, Chiarelli F, Corsello G, Esposito SMR, Ferrara P, Iughetti L, Laforgia N, Maghnie M, Marseglia G, Perilongo G, Pettoello-Mantovani M, Ruggieri M, Russo G, Salerno M, Striano P, Valerio G, Wasniewska M; Italian Academy of Pediatrics, Italian Society of Pediatrics, Italian Society for Pediatric Endocrinology and Diabetes, Italian Society of Adolescent Medicine, Italian Society of Child and Adolescent Neuropsychiatry. Calcaterra V, et al. Ital J Pediatr. 2024 Apr 18;50(1):73. doi: 10.1186/s13052-024-01644-7. Ital J Pediatr. 2024. PMID: 38637868 Free PMC article.
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.
245 results